ZMP
arfgef1
Ensembl ID:
ZFIN ID:
Description:
Im:7138204 protein [Source:UniProtKB/TrEMBL;Acc:Q6DEJ1]
Human Orthologue:
ARFGEF1
Human Description:
ADP-ribosylation factor guanine nucleotide-exchange factor 1(brefeldin A-inhibited) [Source:HGNC Sym
Mouse Orthologue:
Arfgef1
Mouse Description:
ADP-ribosylation factor guanine nucleotide-exchange factor 1(brefeldin A-inhibited) Gene [Source:MGI
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa14568 | Nonsense | Available for shipment | Available now |
sa30078 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa37862 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa17540 | Essential Splice Site | Available for shipment | Available now |
sa778 | Nonsense | F2 line generated | Not yet available |
sa10355 | Nonsense | Available for shipment | Available now |
Mutation Details
This allele has been removed from public view.
Allele Name:
sa30079
Status:
Less stringent filtering
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000092783 | Nonsense | 43 | 1849 | 2 | 39 |
Genomic Location (Zv9):
Chromosome 24 (position 19390225)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 18696379 |
GRCz11 | 24 | 18840798 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCAGTCTATTTGCCTCACTCATGTGAATCTTTTCTTTTCTTTTGCAGAG[G/T]AAATCAAGCAGGAATCGGAGAAATTAAGGTAAGTCGATATCTTGTGCTAC
Long Flanking Sequence:
CAAGCTGGGAATCAAACTTGGGTCACTGTGAGCACCATGGTGCTATATGTCAGCGCACTTAACCACTATTGGTGCCGACAACAAACTAAAATTGTTTATATTGCAAGTTGTTTATCAATTATCACTAGCTTTGAAATATAAAATATGGATGACGTCATTAGCATTAATGGAATGCAGATATAACTACAATTAAAATTGCAACACATACACATTATTTATAGCATTTACAAACATTTTAAGATACAGTTCTTTGAAAGCATCCTTTTTCATTGTATTATTATTTCTAACAAAACAAATATTTACTGCATTTTATCTCAAAAGGCTTCAAAGTCTTGTGTTTACCTGCTAGTACACGGTAAACAAGTCAAGACTGCTTTTGTAGCTGCTTTTAATGCAACCTCATTAGCCTTTACGGTCTGCTATAGGCAGTTTATTTATTTAGTATTGTCAGTCAGTCTATTTGCCTCACTCATGTGAATCTTTTCTTTTCTTTTGCAGAG[G/T]AAATCAAGCAGGAATCGGAGAAATTAAGGTAAGTCGATATCTTGTGCTACACCCCAGCAGTTGATATATTGAACTAGTGTTTCAAAAATCCCCCTTCTTTATTGTTGTCGAGTTCACTGCTTGTAATGAAGCCCTGACATTTTCCAGAGAGTATACCACACGCGGCCTCTTTGTGTTTTAGCTGCTGTTCTGGCCTTATTGTGATTTGTGTGTGTATGTGTGTGAGAGAAAAAACACCCCTTGTGGTCTGTGTTGTTAATGTGCTTGGAGACCTTGCTGTGTGGACACAGGAATGAGACATACTGTGCTCAGGGCTTTCTGCAGGGCCAGGGCGGCCTGTTCCGAGGACCTTCATCTCTCACCCTCTACGTCTATTAATTCACAGCTCACCTGTTTCACCACATCGGCCAGCTTTCTCATCCATGACTGTGTCTTTTGGCTTTTCTTTTCTTTATTGCTTGCATGTGTCTGTTTTAAAATCAGGGAGCACTGCTTTCAAA
Associated Phenotype:
Not determined
Mutation Details
This allele has been removed from public view.
Allele Name:
sa4277
Status:
Allele not cryopreserved
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000092783 | Nonsense | 652 | 1849 | 14 | 39 |
Genomic Location (Zv9):
Chromosome 24 (position 19336539)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 18642693 |
GRCz11 | 24 | 18787112 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTTTCTCTAAACCCTCATCTGAATTTCWTTCCCCTCTTTTTCAATCAGGY[C/T]AAGAAAAGCCTTCAGAGCAGGAGAGCAATGAGTCGAAGCATCCAGAAACG
Long Flanking Sequence:
GTCTCTCAGCTTGTTTCTCTAATCTTTCCAAGGGAAGAAACTGTAAGAGATAAAGAAGTGACCCGACAGCTCATGTTACAGTGATAGCTACCCACTAAATCTTTTACAGTGTTTCCAGTGTGCAATTAGATCCTGCAAACTGCAACCATGGCTTCCACATACCCGACCGCCTATTTGTTTTGCTTTGCACCAACTTCAGATCTGTTACTTGGTGTATACAGGTCATGCTGCTCTTACTCCTGTCCCCATCGTGCTGTTTTTTGTGATACGAGTCAGCAGAGACCAAAGACTTTATTAGAGAAGTGTTGTATTGGGAAACTCATATAGGAAGCAGAGCCAGAGAAAAGGCTCAATACACCAACTCACATTTGAGCCAAACAGGATTTTCAATGAATCATGCTGTCTCTACTCTCTAGGCTGTTTCACAAAACAGGCTCCACACTTCTTCTGCTTTCTCTAAACCCTCATCTGAATTTCATTCCCCTCTTTTTCAATCAGGC[C/T]AAGAAAAGCCTTCAGAGCAGGAGAGCAATGAGTCGAAGCATCCAGAAACGATCAACCGTTACGGCAGCATTAACTCTTTGGACTCCACTGCATCATCAGGCATTGGGAGCTACAGCACACAGATGTCCGGAACAGACAACCCGGAGCAGTTTGAGGTCCTCAAACAACAGAAGGAGATCATAGAGCAAGGCATTGACCTGTAAGCCACCAAGTTGAAACCACAAAACATCAAATCAGTCTCTGCATTATACAAGATGTTGATAAAATCTAGTATATATTTGTATTGAAATTGAAAGAGTGTCTAGTGTCTAGTCTAGTGTTGCTCCTTGAGGGCCACTATTAGCCCTTTTCCACCAAAGATGTTCCAGAGTCTAGTTCCAAATCGTTTTTTTGTCTTTTGATCCCCAAAGCAAGTAAGTTAGTAAGTTTAAGTAGCATCAAAACTTGTCTTTTGTGCCTGCATCAGAGTCCAGAGTTACAGTGACCAATGACACTGTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14568
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000092783 | Nonsense | 692 | 1849 | 14 | 39 |
Genomic Location (Zv9):
Chromosome 24 (position 19336419)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 18642573 |
GRCz11 | 24 | 18786992 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTAACTCTTTGGACTCCACTGCATCATCAGGCATTGGGAGCTACAGCACR[C/T]AGATGTCCGGAACAGACAACCCKGAGCAGTTTGAGGTCCTCAAACAACAG
Long Flanking Sequence:
TGCAATTAGATCCTGCAAACTGCAACCATGGCTTCCACATACCCGACCGCCTATTTGTTTTGCTTTGCACCAACTTCAGATCTGTTACTTGGTGTATACAGGTCATGCTGCTCTTACTCCTGTCCCCATCGTGCTGTTTTTTGTGATACGAGTCAGCAGAGACCAAAGACTTTATTAGAGAAGTGTTGTATTGGGAAACTCATATAGGAAGCAGAGCCAGAGAAAAGGCTCAATACACCAACTCACATTTGAGCCAAACAGGATTTTCAATGAATCATGCTGTCTCTACTCTCTAGGCTGTTTCACAAAACAGGCTCCACACTTCTTCTGCTTTCTCTAAACCCTCATCTGAATTTCATTCCCCTCTTTTTCAATCAGGCCAAGAAAAGCCTTCAGAGCAGGAGAGCAATGAGTCGAAGCATCCAGAAACGATCAACCGTTACGGCAGCATTAACTCTTTGGACTCCACTGCATCATCAGGCATTGGGAGCTACAGCACA[C/T]AGATGTCCGGAACAGACAACCCGGAGCAGTTTGAGGTCCTCAAACAACAGAAGGAGATCATAGAGCAAGGCATTGACCTGTAAGCCACCAAGTTGAAACCACAAAACATCAAATCAGTCTCTGCATTATACAAGATGTTGATAAAATCTAGTATATATTTGTATTGAAATTGAAAGAGTGTCTAGTGTCTAGTCTAGTGTTGCTCCTTGAGGGCCACTATTAGCCCTTTTCCACCAAAGATGTTCCAGAGTCTAGTTCCAAATCGTTTTTTTGTCTTTTGATCCCCAAAGCAAGTAAGTTAGTAAGTTTAAGTAGCATCAAAACTTGTCTTTTGTGCCTGCATCAGAGTCCAGAGTTACAGTGACCAATGACACTGTTTTGTTGTTGTTTTGACACTGTTTTGAACCAAGTTTATTGTAATTAACGAAAATGAATGAAAAAACAAAACTAGAATTGAAAAGCATTTTCTTTAACTGAACTAACCGAAACTGTATTGTGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30078
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000092783 | Nonsense | 825 | 1849 | 17 | 39 |
Genomic Location (Zv9):
Chromosome 24 (position 19332872)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 18639026 |
GRCz11 | 24 | 18783445 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTGCTAATTATGCTATAAACACTAAACTTGTCTCCCTTGTCTCCTTAGG[C/T]AAACACTGTTCGCCAGCGCTGACACCGCATACGTTCTTGCGTATTCAATC
Long Flanking Sequence:
GGGTAAAGTGAGCTCCTTATATCTGCCCTAAAATTAGGGCACTTCAGCAGAACAACCCTCAGCCTGAATGACTCGAGATGTGCTAGGAATACTTTAGCAGATCTACATCCAATACATCCTCTGTCTGGATTTCGAGTTACGAAAGACTTTTTCTGCTATTCATTTCACTACCTACGCAATCAATACGGGACTCATTGGCTGTTTTCTTTCAGATCCAGGTAGGAGAGTTTCTAGGAGACAACGACCGCATCAATAAAGAGGTCATGTATGCCTACGTCGACCAAATGGACTTCCAGGGCAAAGACTTCGTGCCAGCGCTGCGCATGTTCCTGGAGGGTTTCCGTCTGCCCGGCGAAGCCCAGAAAATTGATCGACTGATGGAGAAATTTGCTGCTAGATATTTAGAATGCAACCAAGGGTGAGTTTGACGTTTGCGACAGATTAGCCTAAGTTGCTAATTATGCTATAAACACTAAACTTGTCTCCCTTGTCTCCTTAGG[C/T]AAACACTGTTCGCCAGCGCTGACACCGCATACGTTCTTGCGTATTCAATCATCATGTTGACTACCGATCTGCACAGTCCACAGGTTAGTACACAACACACTGATTGATCACTGGAATTTTAGGCGAATGCGGAATTCGTTTTCTTTTATTCTCGAGTCTATGAATTTTAATGCGAATGTCAGTGCTGGAAAGGGCTGTTGGGCGTTCTGTCTTGATATGTAAGCTAACTCTAGGGTGATGGATGTTTCTGAGACGCAACAGAAAACAAGAGGAAGAGCGGTTCTGATCTGTTGTTTCCTTTATCTTGGCACAGGTGAAGAATAAAATGACGAAAGAGCAATACATCAAGATGAATCGAGGTATCAATGACAGTAAAGATTTACCGGAGGAGTATCTCTCAGCCATTTATGATGAAATCGCAGGGAAGAAAATCTCCATGAAGGAGACAAAGGAGTTAACTCTCAAATCAAATAAGCAAAGTGAGTATTCAGAATATAAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37862
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000092783 | Nonsense | 884 | 1849 | 18 | 39 |
Genomic Location (Zv9):
Chromosome 24 (position 19332463)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 18638617 |
GRCz11 | 24 | 18783036 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGTATCAATGACAGTAAAGATTTACCGGAGGAGTATCTCTCAGCCATTTA[T/A]GATGAAATCGCAGGGAAGAAAATCTCCATGAAGGAGACAAAGGAGTTAAC
Long Flanking Sequence:
CAACCAAGGGTGAGTTTGACGTTTGCGACAGATTAGCCTAAGTTGCTAATTATGCTATAAACACTAAACTTGTCTCCCTTGTCTCCTTAGGCAAACACTGTTCGCCAGCGCTGACACCGCATACGTTCTTGCGTATTCAATCATCATGTTGACTACCGATCTGCACAGTCCACAGGTTAGTACACAACACACTGATTGATCACTGGAATTTTAGGCGAATGCGGAATTCGTTTTCTTTTATTCTCGAGTCTATGAATTTTAATGCGAATGTCAGTGCTGGAAAGGGCTGTTGGGCGTTCTGTCTTGATATGTAAGCTAACTCTAGGGTGATGGATGTTTCTGAGACGCAACAGAAAACAAGAGGAAGAGCGGTTCTGATCTGTTGTTTCCTTTATCTTGGCACAGGTGAAGAATAAAATGACGAAAGAGCAATACATCAAGATGAATCGAGGTATCAATGACAGTAAAGATTTACCGGAGGAGTATCTCTCAGCCATTTA[T/A]GATGAAATCGCAGGGAAGAAAATCTCCATGAAGGAGACAAAGGAGTTAACTCTCAAATCAAATAAGCAAAGTGAGTATTCAGAATATAAACCGTCAAACTTGGAGACAGTAGCAGACAATAGTATGATCAAGTAGTCTCCTACAAAAGCTATGATTGGAAAAATGCTATTTGCTTGCTGGGGTCAGGCAATCCTTTAAAAGTAATTATTATAAAAAATGACTGGGGACTGTGGATTGTCCCACTTACTATTTATTTAATTATTACCGGGAAAAAAAATTGTATTTAACTGTATAATTATTAGGATTTATCATAAAATATTCTAGCAATTGGAAATAATTATTAAAGTAGGTCTGCAATTATTTGTACAATAGTTTTCAGTCAATATTTGTTATAAAAATAAATAAATAAACAATTACAATTTAAGCCAAATTTGGTTTAATTCTCCCCGGTCATTTTTGCCATTTCAGTATTTTCATAAGTTGCGAAAATACCACTCAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17540
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000092783 | Essential Splice Site | 958 | 1849 | 19 | 39 |
Genomic Location (Zv9):
Chromosome 24 (position 19330411)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 18636565 |
GRCz11 | 24 | 18780984 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCCCTTCACCAGCGCCACACATCTWGAGCATGTCAGACCAATGTTTAAGG[T/C]AWTCTCTTCATNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNCAGTA
Long Flanking Sequence:
AGTACCTGATAGCTCCTCTCTTACTGCTATGTTGGTGATAAATAATCACTTATTTTGATTGGTTGAATAATACACCATCCTGGTATATAAAGTGCACATTCTTTTTTTAATTTTTGTGTAAATGCATCAGTATTTATACTGTAAAATGAATTGGAATAGTGCATTAGTAAGCAAGTTGGGACAGTTCTAGTATTAGTTTTCTATTATAGTTAGAGTAATAATAGTAATAATTAGTGCTGGGCAAAAAAAAATGTTATTAATCAAGTCACCTGACTTTAATAGAGGTATAAGGTGAACACTGCTATTTGGTGTTGATTTTAGTTTTTCTGCTGCTTTCTCTGGATCAGGTGTGGCGAGTGAGAAGCAGAGGAGGCTGCTGTATAATGTTGAGATGGAGCAGATGGCAAAAACAGCAAAGGCTCTGATGGAGGCCGTGAGCCACGTTCAAGCCCCCTTCACCAGCGCCACACATCTTGAGCATGTCAGACCAATGTTTAAGG[T/C]AATCTCTTCATGCACATGGACACTACCATTCAAAGATATTGGGATCAGTAAGATTTTTAAAGGTTTTTAAAAGAAGTTGATTCTGGCTATCAAGGCAGCTTTTTATAAGATTGTGTATAAAGATTGAATATAATTGAGATTGAATATAAAATTATAAGATTGTGCAATATTACTGCAATTTAAAATAACCGTTTCCTTATTGAATGAGGCTTAAACTAATCTATTGATGCGATTTCTGGAAATTTTTTAGCATCACTACAGACTTCTGTGTCAAATGATCCTTCAGAAATCATTCTGCTCAAGAAATATTTAATTATTTTTTAGAAAGTGAAGGAAACACACCAATCAAATGTAAAGGCATTTATTTTGTTAAATACGTATTGTTTTGTGTGTTATTTTTTTAAAATAAATGCTGTTATTTTGATCTTCCCTTTTAACAAGGATTTCTAAAAGGTCGAATGTGTCAGTTTTCACAGAAGCAGGAAAAAAACATGTTAATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa778
Status:
F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000092783 | Nonsense | 1167 | 1849 | 25 | 39 |
Genomic Location (Zv9):
Chromosome 24 (position 19321296)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 18627450 |
GRCz11 | 24 | 18771869 |
KASP Assay ID:
554-0683.1 (used for ordering genotyping assays)
KASP Sequence:
GATGGCTGTGCGCTGTCTCGATGGATGAACTGGCCTCCCCAACACACCCT[C/T]GAATGTTCAGTCTGCAGAAGATCGTGGAGATTTCATACTACAATATGGGT
Long Flanking Sequence:
AACAAATCGCAAACAAGTCTTGTGCTTTATTGCGCCGGGTGTCTGATAGGACCCATAAACTTCATAAACAGACAGCCTTAAACTAGAATTTTGAGAAGAATATTCACACTGATAATTCAAATAAACATGACATTTATTTTGTAACACAGTTTTTTTTATCAAGCATGAAAACAGGTGTTACCTACACCTTCACACACGTACACTTTTTTTTATACCATGAACAGTTAAAGCACTTCTTGAAAAAAAAAAAGAGATAAAAACTCAGTACAGCATTTCTTTTGTGAATAAAAAAAAAATGTTCATAGTTTGCATCATATCAGTATTTTTTTCTGGGATGTGTTCCCATAACCTTGGCATTGTACTGACCGAACTCTTTTAGGTCAGGGAGAATTTAAGTGGCAGTTTATTGATCAATGTTGTGTTTTTTTTTTTTTTTAGTGGACTTTGTGCGATGGCTGTGCGCTGTCTCGATGGATGAACTGGCCTCCCCAACACACCCT[C/T]GAATGTTCAGTCTGCAGAAGATCGTGGAGATTTCATACTACAATATGGGTCGTATCAGGTTGCAGTGGTCCAGGATTTGGGAGGTTATAGGGGATCATTTCAATAAGGTGAGTTCAAAAGCAGCGCTGGAAGGAAATCTCTCTGTGAAGAAATGTGTGGCTTTGCACTATATCAGATAAATCTAATGACGCTTTTAAATTTCACCCTGCCTGCGGGAGACCACGTCTAGTAGATTGAAGAAGAGCCAAAAAATGAAAGTACAGCACAATTGTTGCTTAAAGGGACAAGTCATCCACAGTGGAATATGGGTCAGACTGTAGATGTACTGTAATGTATGAAATATAGTGCATATACTACAGGATATATAGCTAAACACTCCTCTCTATGTAACTGTTTTTACTGAGGTAAATATCATGCATCGTGATATAGTTTGTTTTGTTAATGTTCCCAGTTGAAACACAATCAAAGATTGAGACAGCACATTTTTGGAAAAGGAAATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10355
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000092783 | Nonsense | 1611 | 1849 | 35 | 39 |
Genomic Location (Zv9):
Chromosome 24 (position 19301286)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 18607440 |
GRCz11 | 24 | 18751859 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCYTAATTTGATATTATGTTGTGTGTGTGCATTGTGCAGAAGCTCAGGAA[C/T]AGAGGCTGTTTGCTGCGCTACTCATYAAGTGTGTGGTTCAGCTGGAGCTC
Long Flanking Sequence:
AACAATTCATATTTTTAAAGGTCATATATCTTCAAACTTTACAGTTTTGTTCAAAGGGTTGTTGCCAAAGTGTTTTGTTCATATATACTTTGCCTGATTATGTTTACATTAAATGCACCTTAGTTTACAAAACACTCTGAAAAAGTAACTTTTTATGACTCTTCACAGTGTTTTCTGTATTATATATGTATAAATTGCCCAAAATCCAGTGTGTAAAAACACTTGACTGTATCATGACGATTAAAAGAATGATTTTTGAAACTTTGAACTTTGAAACCGACTTCATCCAGACTGAGATAGAAATGTATGCAAATGAGGAAACAATGTTATCGTTTACATTTAATAATTTTTTGCAAGTTTTTAAAAAGGTTTGCAATCAACTAGGAGGTGTGGTGATAACTGTCAGTTAATGTTTTAACCTATTCACTTGCCTTAACCGTATTTTCTTCAGCCTAATTTGATATTATGTTGTGTGTGTGCATTGTGCAGAAGCTCAGGAA[C/T]AGAGGCTGTTTGCTGCGCTACTCATTAAGTGTGTGGTTCAGCTGGAGCTCATTCAGACCATTGACAACATCGTCTTCTTTCCTGCTACCAGTAAGAAAGAAGATGCGGAAAACTTTGCGGCTGCACAGGTACCAGATTTTATTTTTACTATGTTTCAAAATACACATTAGAAAGTTAAATGAGAACGCGATCAGAACATACAGTTGAAGACAAATATTTCACAAGTGATGACCAAGGAACATTTTCAATCTATTACTTTTCTGGAAAGTCATATTTGTTTTAATTTGTCTGGAATAAAAATATTTATATTTTTATTATTATTATTATTTGTTTTTTTACAGCTAAGTTGAATATTATATTTTTTCAATTTTCTACATAACAAACCACTGTTTTACAATGACTTGCTAATTACTCTAGCTTGCCTAGTTTACCTAATTAACCCAGCTAAGCCTTAAAATTGCACTTTAAGCTGAATACTAGTATCTTTCAAAATAACTAGT
Associated Phenotype:
Not determined