Product Details

SNP ID
rs147894987
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.8:143158335 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCAGGGGCTGTGCCCTGCCCCTGCC[A/G]CCCCATTGCACAAATCCTTCTCGCA
Phenotype
MIM: 603625
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
LY6H PubMed Links

Gene Details

Gene
LY6H
Gene Name
lymphocyte antigen 6 complex, locus H
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001130478.1 504 Missense Mutation GCG,GTG A134V NP_001123950.1
NM_001135655.1 504 Missense Mutation GCG,GTG A134V NP_001129127.1
NM_002347.4 504 Missense Mutation GCG,GTG A113V NP_002338.3
XM_017013413.1 504 Missense Mutation GCG,GTG A139V XP_016868902.1
XM_017013414.1 504 Missense Mutation GCG,GTG A113V XP_016868903.1

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