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TTTGACATTTTGCCTTAAGCGGTAA[C/T]GTCTATAAGCACGCTGAATGACAGT
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) - 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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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 | 5980 | Missense Mutation | CAT,CGT | H,R 1891 | NP_002968.1 | |
XM_005246757.2 | 5980 | Missense Mutation | CAT,CGT | H,R 1902 | XP_005246814.1 | |
XM_011511616.2 | 5980 | Missense Mutation | CAT,CGT | H,R 1902 | XP_011509918.1 | |
XM_011511617.2 | 5980 | Missense Mutation | CAT,CGT | H,R 1902 | XP_011509919.1 | |
XM_011511618.2 | 5980 | Missense Mutation | CAT,CGT | H,R 1891 | XP_011509920.1 | |
XM_011511619.2 | 5980 | Intron | XP_011509921.1 | |||
XM_017004668.1 | 5980 | Missense Mutation | CAT,CGT | H,R 1773 | XP_016860157.1 | |
XM_017004669.1 | 5980 | Missense Mutation | CAT,CGT | H,R 1654 | XP_016860158.1 |