Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GAAGGAGGAGAGGTGGTAGAGGAAC[A/T]CCCATCTGTTTTTTCTGGAGTGGAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 182391 | ||||||||||||||||||||
Literature Links: |
SCN3A 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 |
SCN3A - sodium voltage-gated channel alpha subunit 3 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001081676.1 | 6496 | Missense Mutation | AGT,TGT | S,C 1912 | NP_001075145.1 | |
NM_001081677.1 | 6496 | Missense Mutation | AGT,TGT | S,C 1912 | NP_001075146.1 | |
NM_006922.3 | 6496 | Missense Mutation | AGT,TGT | S,C 1961 | NP_008853.3 | |
XM_011511610.2 | 6496 | Missense Mutation | AGT,TGT | S,C 1961 | XP_011509912.1 | |
XM_011511613.2 | 6496 | Missense Mutation | AGT,TGT | S,C 1331 | XP_011509915.1 | |
XM_017004660.1 | 6496 | Missense Mutation | AGT,TGT | S,C 1961 | XP_016860149.1 | |
XM_017004661.1 | 6496 | Missense Mutation | AGT,TGT | S,C 1944 | XP_016860150.1 | |
XM_017004662.1 | 6496 | Missense Mutation | AGT,TGT | S,C 1915 | XP_016860151.1 | |
XM_017004663.1 | 6496 | Missense Mutation | AGT,TGT | S,C 1331 | XP_016860152.1 | |
XM_017004664.1 | 6496 | Intron | XP_016860153.1 | |||
XM_017004665.1 | 6496 | Intron | XP_016860154.1 | |||
XM_017004666.1 | 6496 | Intron | XP_016860155.1 |