Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TGATGAGGAACTGCGCCCTCCGGAA[C/T]ATCACCCTCTCTTGCTCCTGCTTGA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||
Phenotype: |
MIM: 603788 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
KCNG1 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||||||||||||||||||||
Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
|||||
AMR
|
KCNG1 - potassium voltage-gated channel modifier subfamily G member 1 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_002237.3 | 1896 | Missense Mutation | ATA,ATG | I,M 478 | NP_002228.2 | |
XM_006723785.2 | 1896 | Missense Mutation | ATA,ATG | I,M 478 | XP_006723848.1 | |
XM_011528800.1 | 1896 | Missense Mutation | ATA,ATG | I,M 478 | XP_011527102.1 | |
XM_011528801.1 | 1896 | Missense Mutation | ATA,ATG | I,M 478 | XP_011527103.1 | |
XM_011528802.1 | 1896 | Missense Mutation | ATA,ATG | I,M 478 | XP_011527104.1 | |
XM_011528803.2 | 1896 | Missense Mutation | ATA,ATG | I,M 478 | XP_011527105.1 | |
XM_011528804.1 | 1896 | Missense Mutation | ATA,ATG | I,M 478 | XP_011527106.1 | |
XM_011528805.2 | 1896 | Missense Mutation | ATA,ATG | I,M 478 | XP_011527107.1 | |
XM_011528806.1 | 1896 | Missense Mutation | ATA,ATG | I,M 478 | XP_011527108.1 |