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CTGTAGGTGACTCCGCCTTTTGATC[C/T]CCGATTCTGTGAAGTGAGAGAAAAA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
1 submissions
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Phenotype: |
MIM: 608162 | ||||||||||||||||||||
Literature Links: |
VTCN1 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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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 |
VTCN1 - V-set domain containing T cell activation inhibitor 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001253849.1 | 1146 | Intron | NP_001240778.1 | |||
NM_001253850.1 | 1146 | Intron | NP_001240779.1 | |||
NM_024626.3 | 1146 | Intron | NP_078902.2 | |||
XM_011542143.2 | 1146 | Missense Mutation | GAG,GGG | E,G 294 | XP_011540445.2 | |
XM_017002335.1 | 1146 | Missense Mutation | GAG,GGG | E,G 249 | XP_016857824.1 |