Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GAGTAAATCATCATCTCTGTCTCCA[C/T]CTTTTATGTATATACTTGATATATT
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603415 | |||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
LOC101929680 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)
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EAS
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African American - Not Available | YRI (Yoruba) - Not Available | ||||||
SAS
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Chinese - Not Available | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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LOC101929680 - uncharacterized LOC101929680 | ||||||
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There are no transcripts associated with this gene. |
SCN9A - sodium voltage-gated channel alpha subunit 9 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_002977.3 | 6031 | Missense Mutation | GAT,GGT | D,G 1908 | NP_002968.1 | |
XM_005246757.2 | 6031 | Missense Mutation | GAT,GGT | D,G 1919 | XP_005246814.1 | |
XM_011511616.2 | 6031 | Missense Mutation | GAT,GGT | D,G 1919 | XP_011509918.1 | |
XM_011511617.2 | 6031 | Missense Mutation | GAT,GGT | D,G 1919 | XP_011509919.1 | |
XM_011511618.2 | 6031 | Missense Mutation | GAT,GGT | D,G 1908 | XP_011509920.1 | |
XM_011511619.2 | 6031 | Intron | XP_011509921.1 | |||
XM_017004668.1 | 6031 | Missense Mutation | GAT,GGT | D,G 1790 | XP_016860157.1 | |
XM_017004669.1 | 6031 | Missense Mutation | GAT,GGT | D,G 1671 | XP_016860158.1 |
Set Membership: |
HapMap |