Busch Lab

ZMP

dnmt3

Ensembl ID:
ENSDARG00000057830
ZFIN ID:
ZDB-GENE-990712-11
Description:
DNA (cytosine-5-)-methyltransferase 3 [Source:RefSeq peptide;Acc:NP_571461]
Human Orthologue:
DNMT3B
Human Description:
DNA (cytosine-5-)-methyltransferase 3 beta [Source:HGNC Symbol;Acc:2979]
Mouse Orthologue:
Dnmt3b
Mouse Description:
DNA methyltransferase 3B Gene [Source:MGI Symbol;Acc:MGI:1261819]

Alleles

There are 10 alleles of this gene:

Allele Name Consequence Status Availability
sa24284 Nonsense Available for shipment Available now
sa43937 Nonsense Mutation detected in F1 DNA Not yet available
sa43936 Nonsense Mutation detected in F1 DNA Not yet available
sa14072 Nonsense Available for shipment Available now
sa37658 Nonsense Mutation detected in F1 DNA Not yet available
sa9741 Nonsense Available for shipment Available now
sa24283 Essential Splice Site Available for shipment Available now
sa43935 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa24284
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000080545 Nonsense 153 1448 4 24
ENSDART00000126841 Nonsense 153 1448 5 25

The following transcripts of ENSDARG00000057830 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 23 (position 17169993)
Other Location(s):
Assembly Chromosome Position
GRCz10 23 17072932
GRCz11 23 16999275
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATCTATTTTCTTTATTCATAGTTGAAAAGGAAAATGTGTCAAGCCTCTA[C/A]AATACTGAAGAAACCAGTTCAAACCAGAAAACGCAACATGTTGAGAAGAC
Long Flanking Sequence:
ACGTAACTAAAGTGAATTTCACAGCAGAGGAGAACCTAGACATCTTGAATAATTATAATCTGCTACAGGAAGCTTTCAGCAAAGCACAGATTCAAAAAGTGAGTACACAATAGAATTCCACTGTAGAATGGAAAGTTTATGATGTACAATTTCAGTTAAATGAATGAATTATAGTGGTCAACACAGGCAACAGGCATCTTTTTTCGTCTTTATAGGAGCTGGAGCTGACATTGCTGGTGAATGGAGATATTATGACAACGTGTGATTTGCTTACATGGTTCAAAGACATGTATGATCACAATTTTGCAAAGCAGAAATGTAACCCACAGGTGGCCTTCATTAAACCTGAAGTAGTTTCATTGAAATCAAGCAGAGAGTTTGAAACAAGTAGGTGTTTACTTTTTGTGTTTGTAATAATTCTGTAAAATTGATATTTAAGTTTAATGATGTCATCTATTTTCTTTATTCATAGTTGAAAAGGAAAATGTGTCAAGCCTCTA[C/A]AATACTGAAGAAACCAGTTCAAACCAGAAAACGCAACATGTTGAGAAGACGTCACAAGAGTCAGTCTCCTGGAGTCCACTCACATCTTTCATAAGAAAGTATGGCTCATCCACCTTAACTGATGATGAATCAAACAATGTGAATAGTAAGGATTGTCCAGGCCAGAAATCTTTTGGAGACATTACACCATTCTGGAGACAGACTCCATACTGCCTTTATCTTTTACATGGAGTGGAGCTCGAGGATGACAAGAAGGCCAGTGTGCTCTTGTTGGGCTTTTTTGACAAAGAAACTGGGGAAAACAAAATCAGACTACTGGATGTTGTCTATCCAACAAAAGAGTCCACTGAAGACATCTGCAACTACATCTTGGACACTCTGAGGAAGATCGGAATACCTTTATTCAACATGGCCATATTATATTCAGATTTTCCAGATCACGAACATCTTGTAGCTGGTCTACAGTTAATGAAAGCTGAGATTGTGTCTTTATGTGGACT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa43937
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000080545 Nonsense 650 1448 5 24
ENSDART00000126841 Nonsense 650 1448 6 25

The following transcripts of ENSDARG00000057830 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 23 (position 17168364)
Other Location(s):
Assembly Chromosome Position
GRCz10 23 17071303
GRCz11 23 16997646
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTGTGTGTGTGTAATAATCTATATTTCAGATGTTTCAACAAACTGACTA[T/G]CTCAAGATGATGAGAAAAGAGGACTGTGAGGAGAAGGATATGATGGAGGA
Long Flanking Sequence:
GTTAATATTGTCAAACGTCTGCCTCTCCCTGATTCCACCCTGAGAAACTTGTCGTTGGTGTTGAGTCCAGGAAAAAAGCTTGAAGTGACGGGCAAAATGGTCCAAGATTTAGGCGTCGGTTTCGGTGTTTGCATAAGGCCAGACAATGTCAGCCTGCTAACGGATGAGTTTTTGGAGTACCAGTTAATTGATGGGGGTGACACTGGCTCGGTCGACCAGCCAACTGAGAAGTACTGGCAAACAGAGCTGAGGATTATGGGAAATGCATCTAATTTCGGGAAATTAATTGTTAGCTTGCTGGCCCTTCCCAAAACACTGAAAAAAGAGATCATTTTTAAACAGGTGAGTTACTGACTTTATGAAGAGCTTCAGAAACCTAATTATCATTGATCATATGTCAATCCATCTAGAACCATGTACATTTCACTCACGCAGACATCTAAATGTTTTTTTGTGTGTGTGTAATAATCTATATTTCAGATGTTTCAACAAACTGACTA[T/G]CTCAAGATGATGAGAAAAGAGGACTGTGAGGAGAAGGATATGATGGAGGATGATGTTACGGACAGCAGCTCATATAAAAGCGCTCCATCACATCTCAGCCCAGAGACGCAGGGAAGCAGCATATCCGGTAAAAATACAAACTCCACAAAGATCAAAACATGCCAAGAAGCCAATCTGTACTACTGACTTTGGATCACAAATGAATTTTTATTTCAGATGTCATTGACCTTACTGAAATGGATGAGATAGGTCCAGTGGAAATAGAGGACATTGCACCAATGGATGTGGATGATATTGTGTCAATTTCTTCTGATTCCGAAACAGAAAACCAGAAAGGTCTCAGGCGCTCTTCAGATATACCAAAATAGGGGTATTTTGTCCGGCAGTTTTGCAGCAGTGAGACAGGTCTAAGTAACTTACCTTTCCCTTCTTTTTACAGTCAATGTTCCACATGTATCTATAGTCTTAGATGATGATGATGATGATGATGATGAAATGAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa43936
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000080545 Nonsense 762 1448 7 24
ENSDART00000126841 Nonsense 762 1448 8 25

The following transcripts of ENSDARG00000057830 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 23 (position 17167838)
Other Location(s):
Assembly Chromosome Position
GRCz10 23 17070777
GRCz11 23 16997120
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGATGATGATGATGATGAAATGACAGATGATGATGACGATTATGGCTGT[G/T]AAGCTGGCGAAGTCATGTGGAAGTATTCGGTAAATATTTTCCCATTGGTT
Long Flanking Sequence:
GTGAGGAGAAGGATATGATGGAGGATGATGTTACGGACAGCAGCTCATATAAAAGCGCTCCATCACATCTCAGCCCAGAGACGCAGGGAAGCAGCATATCCGGTAAAAATACAAACTCCACAAAGATCAAAACATGCCAAGAAGCCAATCTGTACTACTGACTTTGGATCACAAATGAATTTTTATTTCAGATGTCATTGACCTTACTGAAATGGATGAGATAGGTCCAGTGGAAATAGAGGACATTGCACCAATGGATGTGGATGATATTGTGTCAATTTCTTCTGATTCCGAAACAGAAAACCAGAAAGGTCTCAGGCGCTCTTCAGATATACCAAAATAGGGGTATTTTGTCCGGCAGTTTTGCAGCAGTGAGACAGGTCTAAGTAACTTACCTTTCCCTTCTTTTTACAGTCAATGTTCCACATGTATCTATAGTCTTAGATGATGATGATGATGATGATGATGAAATGACAGATGATGATGACGATTATGGCTGT[G/T]AAGCTGGCGAAGTCATGTGGAAGTATTCGGTAAATATTTTCCCATTGGTTTTATGTTTTAAGTTTATTTCTGGGTGTCTTGATTAAACTTTTTGTTTTTCTCCTAGAAAAATAAAGGAAATACACAAAATGAGATGACAGATAATACATACCAGGTAAATTCTTTAATATTTATATATAAAAAAATTATGACCCAATTTCAGCATTTATAACAGGGCATCTGTGGGGTCTTAAAAGTATTTAAAATTGATAAATCAATTTAGAGAAATTTAAGGCCCTTAAAAAGTATTGAAAAGTCTTAAATGCTATTTTACAAGGTTTTTAATTCGATATCAGTATGTTAAAGTTTACCTGAATTAATTTTTTATATTTTTTATGAATGCTGTGTAGTTTATGAAATAAAAAATATCCAGCTAGATTTGACACCACACTGCTTTGTTTACTTCAGTAAGCAGAGAAAACACTGTTAATCCTGCTGTTGTAAAGGCAGTACGTGCTGGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa14072
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000080545 Nonsense 770 1448 7 24
ENSDART00000126841 Nonsense 770 1448 8 25

The following transcripts of ENSDARG00000057830 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 23 (position 17167812)
Other Location(s):
Assembly Chromosome Position
GRCz10 23 17070751
GRCz11 23 16997094
KASP Assay ID:
2261-7500.1 (used for ordering genotyping assays)
KASP Sequence:
GATGATGATGACGATTATGGCTGTGAAGCTGGCGAAGTCATGTGGAAGTA[T/A]TCGGTAAATATTTTCCCATTGGTTTTATGTTTTAAGTTTATTTCTGGGTG
Long Flanking Sequence:
GATGTTACGGACAGCAGCTCATATAAAAGCGCTCCATCACATCTCAGCCCAGAGACGCAGGGAAGCAGCATATCCGGTAAAAATACAAACTCCACAAAGATCAAAACATGCCAAGAAGCCAATCTGTACTACTGACTTTGGATCACAAATGAATTTTTATTTCAGATGTCATTGACCTTACTGAAATGGATGAGATAGGTCCAGTGGAAATAGAGGACATTGCACCAATGGATGTGGATGATATTGTGTCAATTTCTTCTGATTCCGAAACAGAAAACCAGAAAGGTCTCAGGCGCTCTTCAGATATACCAAAATAGGGGTATTTTGTCCGGCAGTTTTGCAGCAGTGAGACAGGTCTAAGTAACTTACCTTTCCCTTCTTTTTACAGTCAATGTTCCACATGTATCTATAGTCTTAGATGATGATGATGATGATGATGATGAAATGACAGATGATGATGACGATTATGGCTGTGAAGCTGGCGAAGTCATGTGGAAGTA[T/A]TCGGTAAATATTTTCCCATTGGTTTTATGTTTTAAGTTTATTTCTGGGTGTCTTGATTAAACTTTTTGTTTTTCTCCTAGAAAAATAAAGGAAATACACAAAATGAGATGACAGATAATACATACCAGGTAAATTCTTTAATATTTATATATAAAAAAATTATGACCCAATTTCAGCATTTATAACAGGGCATCTGTGGGGTCTTAAAAGTATTTAAAATTGATAAATCAATTTAGAGAAATTTAAGGCCCTTAAAAAGTATTGAAAAGTCTTAAATGCTATTTTACAAGGTTTTTAATTCGATATCAGTATGTTAAAGTTTACCTGAATTAATTTTTTATATTTTTTATGAATGCTGTGTAGTTTATGAAATAAAAAATATCCAGCTAGATTTGACACCACACTGCTTTGTTTACTTCAGTAAGCAGAGAAAACACTGTTAATCCTGCTGTTGTAAAGGCAGTACGTGCTGGATTACCAGTTTTTTGAGTATATAAATA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa37658
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000080545 Nonsense 862 1448 10 24
ENSDART00000126841 Nonsense 862 1448 11 25

The following transcripts of ENSDARG00000057830 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 23 (position 17162823)
Other Location(s):
Assembly Chromosome Position
GRCz10 23 17065762
GRCz11 23 16992105
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCATTAGCCAAGTGCTTTTGTTCTAATTCCTTCGCTACAGTAATGGCATA[T/G]AAAGATGCAATTTTCAGTTCTCTGCAGGTAAGGCAAATTCTGTTTCTAGT
Long Flanking Sequence:
GTTTGTTTAATTAGGGTTGGAACTAAACTGCGCAGAGCTGCCACTCTCCAGGAACTGAGTTTGACACCTATGCTGTAAAGTATAACATTCTGGTAACAGTTAATTTAACATGGAACAGGAGAAAGTGTAACAAAATATAGTAAGACTCTTATCATCTAATGAGTGTTGTGTTCCTCATTTTAGGGTGGTTTTTCAGTCGGTGAGATGGTTTTGGGACCAATTGAGGGCTTTGGTCTTTGGCCTGGACTAGTTCAGAGCTGGGACAGTGAGAGGCCTTGTGGCTCCATGCGTAAAGTGATTTTCTTTGGGAACGGGATGCAGACAGAAGTAAAAAAATTAAAATTAATTATGTATGCATGCTTTTGAATGTTTTACTCACTCTATAAATAAAAAATACACATAACAAATGATCTATTTCAGGTCCAAGCAGACAGTCTTCTGCCCTTCTCTTCATTAGCCAAGTGCTTTTGTTCTAATTCCTTCGCTACAGTAATGGCATA[T/G]AAAGATGCAATTTTCAGTTCTCTGCAGGTAAGGCAAATTCTGTTTCTAGTGCACTGTAGTGATAATATTATTTCACATTGTTTGCAGTTCTTCTTGACTATGTTTGTGGCATAAGAAAATATTGAAACGATAAGGTCCAGCACATCTAGCCAAAGGACCCTTTTCACAAGACTGTAACAACGCGTTTAACGGTCATCATAATCTTAAATATTTAAAAGCTAAAATATTAAGATTTTTTAAAAAACGTATGAACATTTATATGCTGTTATGTATGTATTATGTCATCTTTGCGTCAAATTATAAAAAAAACAAATTACAGCTTATTTCTAATGCAGTGTCTATGGGTCTTAGAGTATATTTGACATTATTCTCTCCTCTGGCTGCCGTCATCAGTCTCACTGATAGCAGAGTAAAAAACTCTCCCATTCATTGTGCTCTTAAGTTTACCCAGCTATGACTGCTTCTACTGCTGAAAAACCCGCAAATGTAAAAAGTGTCAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa9741
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000080545 Nonsense 984 1448 12 24
ENSDART00000126841 Nonsense 984 1448 13 25

The following transcripts of ENSDARG00000057830 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 23 (position 17160480)
Other Location(s):
Assembly Chromosome Position
GRCz10 23 17063419
GRCz11 23 16989762
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCAAAATGGAATGGCAGATCAATGCAGACMGTTAAGATCCGTAGAAAATA[T/G]AAACAGCGGAATAAGAATATCATCCCAACTGTACAGATCGAGTCCAGGCA
Long Flanking Sequence:
TAAGCACACAAATGTCTTTGATTCTAGGTGGCTTCCAGACGCAGTAGAATGTTTTTTTCTCCTGAGAGTGAATCTAAGGATGAACTCCTTAGAGTCATGTTGAACTGGGCCTTTGGAGGCTTTGAACCACTGGGTGCAGATGGACTCCAGCCTCAAGCAGAATACAGTGGTATGCAACAACAACTGAATGACTTTCTTTGACCTCAGTGTTTTACTTCAGTATGCGGCATATTGTTTTCAATGCAGTATTCATATAATTTATTCTATTCTCTTTCTTTCTTATACACTTTCTTATATACAATAGTGAAAGTGAAAAAGGGAAAGCGCAAGAACCCTACAGGAAAGTTGTTTAATTTAACTGTGCCCCTCAATAAAATCCCTGAATCTCTGGACCTGAACAATGGCTCAGTAGATCTCGGGACAACAGACGCCGACAAGAAACGCTTGTATTCAAAATGGAATGGCAGATCAATGCAGACCGTTAAGATCCGTAGAAAATA[T/G]AAACAGCGGAATAAGAATATCATCCCAACTGTACAGATCGAGTCCAGGCAAAACAGCCAAAAAAGACGTATGTGCATGCTTTATATTCATTGCTGCTATTAAAACTGTGATGACAAATAAACAAAGAAACCTGATGTTTACTGAACTTTTTCCACAGATCAAATGGTGCATGAATTTCTTAAAAACAAGAGAAAGATTGAAGGTGGGACACTCTTTTATAAGTATTGTGTTAATTTAGGTTGATAATGAGGAAAGTTTAACCGTATGTCATATCCTTTTCCTCAGATTTCTGCTTATCATGTGGCAGTATGTCCGTTGACATCATTCATCCACTCTTCGAAGGAAAGCTGTGTACAAACTGCAAGGTATTACATGTAGTTTAACAGCTTTAGTTCTCAACACACATGGATTTAGTTATTTCAGCTACACCTGTAACTAAATGTTACAAATATAAAACATCCTCATGCTGGGTTCACATTGCTTCATGTCCTCTAAATTAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa24283
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
T > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000080545 Essential Splice Site 1255 1448 19 24
ENSDART00000126841 Essential Splice Site 1255 1448 20 25

The following transcripts of ENSDARG00000057830 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 23 (position 17157459)
Other Location(s):
Assembly Chromosome Position
GRCz10 23 17060398
GRCz11 23 16986741
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCATGTAATGACTTGTCCATAGTCAATCCTGCTCGGAAAGGCTTGTATGG[T/G]AAGACAAAAGTACTGAAAGACAAAGTTCAAGCATTAAATCATAAAATATT
Long Flanking Sequence:
ATGTAAAGGCAGGAAACGCTGTTTGTCAATCATGTAAATAAAAATATATATATAATCTGTAAATAAAAAAGACCTGTTCAGGTAAAGGGATTTGTCTCTTTAGAAGACATGGATTAAACCTTTCTATATACTTATGTGTTATATTTAGTCTTGTTTATGTTTTATACCATCAGATTTACTTAGTGAACTGACTTTCAATGAAGGAACAGAAATAACTCAGATTTAAATGTCTTATTTTTTTGTTTTGTCAATAAATAAATATTCTATAGGTTTGGAATATAAGGGAGGGTAAATTATGAGATGCATTTTGAGTTCAAACATCTCTTCGTACTTTTTGGGACTTTAGTCACGCATATCAAAAAGACTCCTCGGCAGTCTGCTTATTGATTGTATTCTTCATTTTTTTAGATAGAGCAGTGGGGTCCATTTGATCTTCTCATTGGTGGAAGTCCATGTAATGACTTGTCCATAGTCAATCCTGCTCGGAAAGGCTTGTATGG[T/G]AAGACAAAAGTACTGAAAGACAAAGTTCAAGCATTAAATCATAAAATATTCATTTGCCAGGGCGTGACATTAACTTTTTTGATCACCAGCCACTAATGCCAGTAGTTTTATAATGTTACTAGCCACTCGCCATTTTCACTAGCCAATTTTATTGTTGGGAAAATGTATTTTATATGCATAAATGTTACTTTGGCATGCTAAAAAATTGACATTTCTTGTTATATCCACGTCTCCTTATTAATTTAACTTTTTTGACTTTTCATGACTTTTTAGGGCCCAACACTGGATTTACCGATTTTTCTCTGCACATCAAACTAAATATTTCCTTGCCACAATTTTTTTTAAATAATGTGGCAAAACAAGCTAAATGTAGCAGTATATATACAATTTTTATTCTATAATTTAAAAAAGAAAACAATTGACAATTTAAAAAATTATTATCATTTATCTAAAACTATACACAGTAGTTTGTCTGGGCTAAAGGTCCCAGATCATCAGTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa43935
Status:
Mutation detected in F1 DNA
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
ENSDART00000080545 Nonsense 1357 1448 23 24
ENSDART00000126841 Nonsense 1357 1448 24 25

The following transcripts of ENSDARG00000057830 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 23 (position 17154762)
Other Location(s):
Assembly Chromosome Position
GRCz10 23 17057701
GRCz11 23 16984044
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATAATGATGTCACAGTGGTCGTAACACTGAAATGTACTATTTTCCAGTA[T/A]GAAAAAGTTCGCACTATCACTACACGGCAAAACTCCCTGAAGCAGGGCAC
Long Flanking Sequence:
CTGATACCAAATGATCAACTAAAAGTCAAGATATTAGTTGTTGTTCCTAAAATTTGGATAGGTGACAAGACTTTTGTCAGGTAGTGGATATTGGCATAGTTTTAAAAATGTATTTGTTTGCTTTTTTATTTGTGTGGTTTTTGTTTTTAGTGTAACCCTGTGCTTGTTGATGCCGTGAAAGTGAGTCCAGCTCACAGAGCAAGATACTTCTGGGGGAACATACCTGGCATGAACAGGTGCGTCAGTGGTATCGTGTAACCATCACACTTCATGAAATATACAATCACCTGTTTTAAGTGTATGAACATGACAGTATACCTCATACCTTTTTATTACATTTTGCCAGACCAATCATAGCATCTCAGAATGATAAACTCTGTCTTCAAGAATGTCTGGAGCCTGGCCGCACTGCAAAGGTTAGTCATCTAACCTAATAAAAGTACACTTGACTATAATGATGTCACAGTGGTCGTAACACTGAAATGTACTATTTTCCAGTA[T/A]GAAAAAGTTCGCACTATCACTACACGGCAAAACTCCCTGAAGCAGGGCACCAATGATGCACATTTCCCCGTCACCATGAATGGTAAAGATGACCACATATGGATCACAGAATTGGAGAAGTATGTTTTTTTTGTCTACTTTTTAACAATAAAATTGTGTAAAGAACTATAAATTGAATGATGAATGTTTTATTTATGATGATTCTGACACTTCCACAGAATATTTGGATTTCCGAAGCATTACACTGATGTGAAAAGCATGGGTCGTCCGCAGAGGCAGAGAGTATTGGGGAAGTCCTGGAGCGTTCCTGTCATTAGGCATCTTTTAGCACCACTGAAGGATTACTTTGCTTGTGACGAATTCCCTGTGAAATGAAGAGAGGCTACGATGAGGATTTTAATTCTATTTTGGTCAATGTAAAAAGACTCAGGGACACACAACTATGTTGCTTTTTAAGTGTTTTTTAACTTTTTTAATGAAACTGTTATGACTAGCCGAAG
Associated Phenotype:
Not determined