Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AAAGGCCTTTTGAATAATAGCAGCA[A/C]CTCTTTCCTCTTCCTTTCTCTTGGT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 604385 | ||||||||||||||||||||
Literature Links: |
SCN11A PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||
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 |
SCN11A - sodium voltage-gated channel alpha subunit 11 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001287223.1 | 4015 | Missense Mutation | GGT,GTT | G,V 1736 | NP_001274152.1 | |
NM_014139.2 | 4015 | Missense Mutation | GGT,GTT | G,V 1736 | NP_054858.2 | |
XM_011533321.2 | 4015 | Missense Mutation | GGT,GTT | G,V 1515 | XP_011531623.1 | |
XM_017005647.1 | 4015 | Missense Mutation | GGT,GTT | G,V 1861 | XP_016861136.1 | |
XM_017005648.1 | 4015 | Missense Mutation | GGT,GTT | G,V 1670 | XP_016861137.1 | |
XM_017005649.1 | 4015 | Missense Mutation | GGT,GTT | G,V 1736 | XP_016861138.1 | |
XM_017005650.1 | 4015 | Missense Mutation | GGT,GTT | G,V 1736 | XP_016861139.1 | |
XM_017005651.1 | 4015 | Missense Mutation | GGT,GTT | G,V 1645 | XP_016861140.1 | |
XM_017005652.1 | 4015 | Intron | XP_016861141.1 | |||
XM_017005653.1 | 4015 | Missense Mutation | GGT,GTT | G,V 1204 | XP_016861142.1 |