Product Details

SNP ID
rs17111391
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.10:96190730 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TTAGACTTAATTAGCTGCTTTATCA[C/T]TTCACTGCTGTCTGAAGTACACAGT
Phenotype
MIM: 604515
Polymorphism
C/T, 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 2601 Intron NP_001107566.1
NM_001258440.1 2601 Intron NP_001245369.1
NM_001258441.1 2601 Intron NP_001245370.1
NM_001258442.1 2601 Intron NP_001245371.1
NM_013314.3 2601 Intron NP_037446.1
XM_011539728.2 2601 UTR 3 XP_011538030.1
XM_017016159.1 2601 UTR 3 XP_016871648.1

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