Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TCCTAAGCGGGAGGACTCACCGAGA[G/T]AGATACCCTTTCCATATTGGATAAA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 616804 | ||||||||||||||||||||
Literature Links: |
VSTM1 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 |
VSTM1 - V-set and transmembrane domain containing 1 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001288791.1 | 1069 | Missense Mutation | ATC,CTC | I,L 108 | NP_001275720.1 | |
NM_001288792.1 | 1069 | Missense Mutation | ATC,CTC | I,L 165 | NP_001275721.1 | |
NM_001288793.1 | 1069 | Missense Mutation | ATC,CTC | I,L 76 | NP_001275722.1 | |
NM_198481.3 | 1069 | Missense Mutation | ATC,CTC | I,L 196 | NP_940883.2 | |
XM_011526845.1 | 1069 | Missense Mutation | ATC,CTC | I,L 324 | XP_011525147.1 | |
XM_011526846.1 | 1069 | Missense Mutation | ATC,CTC | I,L 294 | XP_011525148.1 | |
XM_011526847.1 | 1069 | Silent Mutation | CTA,CTC | L,L 316 | XP_011525149.1 | |
XM_011526848.1 | 1069 | Missense Mutation | ATC,CTC | I,L 263 | XP_011525150.1 | |
XM_011526849.1 | 1069 | Missense Mutation | ATC,CTC | I,L 226 | XP_011525151.1 | |
XM_017026666.1 | 1069 | Intron | XP_016882155.1 |