Product Details

SNP ID

rs164122

Assay Type

Validated

NCBI dbSNP Submissions

79

Location

Chr.1:162398567 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

ATTGAGCAAAGTGTAACAGTATACG[C/T]TTTGGGGAGGGCTTGAAGGGCTAGA

Phenotype

MIM: 608510

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

SH2D1B PubMed Links

Gene Details

Gene

SH2D1B

Gene Name

SH2 domain containing 1B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_053282.4		Intron			NP_444512.2

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