Product Details
- SNP ID
-
rs201232183
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.7:107593967 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- TGTTCTGTAATAGATGCTGTGAGAG[A/T]AGTAAGGAAATATTCCTCAGTTCAT
- Phenotype
-
- Polymorphism
- A/T, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
BCAP29
PubMed Links
Gene Details
- Gene
- BCAP29
- Gene Name
- B-cell receptor-associated protein 29
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001008405.2 |
541 |
Missense Mutation |
GAA,GTA |
E69V |
NP_001008405.1 |
NM_018844.3 |
541 |
Missense Mutation |
GAA,GTA |
E69V |
NP_061332.2 |
XM_006716051.2 |
541 |
Missense Mutation |
GAA,GTA |
E69V |
XP_006716114.1 |
XM_011516406.2 |
541 |
Missense Mutation |
GAA,GTA |
E69V |
XP_011514708.1 |
XM_011516407.1 |
541 |
Missense Mutation |
GAA,GTA |
E69V |
XP_011514709.1 |
XM_011516408.2 |
541 |
Missense Mutation |
GAA,GTA |
E69V |
XP_011514710.1 |
XM_011516409.2 |
541 |
Missense Mutation |
GAA,GTA |
E69V |
XP_011514711.1 |
XM_017012436.1 |
541 |
Missense Mutation |
GAA,GTA |
E69V |
XP_016867925.1 |
XM_017012437.1 |
541 |
Missense Mutation |
GAA,GTA |
E69V |
XP_016867926.1 |
XM_017012438.1 |
541 |
Missense Mutation |
GAA,GTA |
E69V |
XP_016867927.1 |
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