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GGGCAGGGACAGAGCTGAGCTCTCC[A/G]TCCTCTGGTCGCTCCACCCACCAGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
32 submissions
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Phenotype: |
MIM: 606644 MIM: 600932 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
IGSF8 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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IGSF8 - immunoglobulin superfamily member 8 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001206665.2 | 1539 | Silent Mutation | GAC,GAT | D,D 486 | NP_001193594.1 | |
NM_001320247.1 | 1539 | Silent Mutation | GAC,GAT | D,D 486 | NP_001307176.1 | |
NM_052868.5 | 1539 | Silent Mutation | GAC,GAT | D,D 486 | NP_443100.1 | |
XM_006711631.3 | 1539 | Silent Mutation | GAC,GAT | D,D 469 | XP_006711694.1 | |
XM_011510159.2 | 1539 | Silent Mutation | GAC,GAT | D,D 464 | XP_011508461.1 | |
XM_017002835.1 | 1539 | Silent Mutation | GAC,GAT | D,D 486 | XP_016858324.1 | |
XM_017002836.1 | 1539 | Silent Mutation | GAC,GAT | D,D 486 | XP_016858325.1 | |
XM_017002837.1 | 1539 | Silent Mutation | GAC,GAT | D,D 486 | XP_016858326.1 | |
XM_017002838.1 | 1539 | Silent Mutation | GAC,GAT | D,D 464 | XP_016858327.1 | |
XM_017002839.1 | 1539 | Silent Mutation | GAC,GAT | D,D 464 | XP_016858328.1 | |
XM_017002840.1 | 1539 | Silent Mutation | GAC,GAT | D,D 464 | XP_016858329.1 |
KCNJ9 - potassium voltage-gated channel subfamily J member 9 | ||||||
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There are no transcripts associated with this gene. |