Product Details

SNP ID
rs202240472
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.10:96192057 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CAATAAGAACCAAAGGACTATGTTG[A/G]TGATTCCTGATGATTTCAGCAACAC
Phenotype
MIM: 604515
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
BLNK PubMed Links

Gene Details

Gene
BLNK
Gene Name
B-cell linker
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001114094.1 1274 Silent Mutation CAC,CAT H406H NP_001107566.1
NM_001258440.1 1274 Silent Mutation CAC,CAT H377H NP_001245369.1
NM_001258441.1 1274 Silent Mutation CAC,CAT H354H NP_001245370.1
NM_001258442.1 1274 Silent Mutation CAC,CAT H272H NP_001245371.1
NM_013314.3 1274 Silent Mutation CAC,CAT H429H NP_037446.1
XM_011539728.2 1274 Silent Mutation CAC,CAT H429H XP_011538030.1
XM_017016159.1 1274 Silent Mutation CAC,CAT H406H XP_016871648.1

View Full Product Details