Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GTCTCCCCGCGGTACACTGTGCCTC[C/T]TGCTAGCCATGCCACAGCCTCCAGC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
12 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 |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
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 | 1426 | Missense Mutation | AGA,GGA | R,G 449 | NP_001193594.1 | |
NM_001320247.1 | 1426 | Missense Mutation | AGA,GGA | R,G 449 | NP_001307176.1 | |
NM_052868.5 | 1426 | Missense Mutation | AGA,GGA | R,G 449 | NP_443100.1 | |
XM_006711631.3 | 1426 | Missense Mutation | AGA,GGA | R,G 432 | XP_006711694.1 | |
XM_011510159.2 | 1426 | Missense Mutation | AGA,GGA | R,G 427 | XP_011508461.1 | |
XM_017002835.1 | 1426 | Missense Mutation | AGA,GGA | R,G 449 | XP_016858324.1 | |
XM_017002836.1 | 1426 | Missense Mutation | AGA,GGA | R,G 449 | XP_016858325.1 | |
XM_017002837.1 | 1426 | Missense Mutation | AGA,GGA | R,G 449 | XP_016858326.1 | |
XM_017002838.1 | 1426 | Missense Mutation | AGA,GGA | R,G 427 | XP_016858327.1 | |
XM_017002839.1 | 1426 | Missense Mutation | AGA,GGA | R,G 427 | XP_016858328.1 | |
XM_017002840.1 | 1426 | Missense Mutation | AGA,GGA | R,G 427 | XP_016858329.1 |
KCNJ9 - potassium voltage-gated channel subfamily J member 9 | ||||||
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There are no transcripts associated with this gene. |