Product Details

SNP ID

rs56261530

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:4280210 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ACTTCGAGGACCCCTATGAGGACGC[C/G]GAGAGCCGCTTGGAGCCGGACCCCG

Phenotype

MIM: 610481

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

SHD PubMed Links

Gene Details

Gene

SHD

Gene Name

Src homology 2 domain containing transforming protein D

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_020209.3	1610	Silent Mutation	GCC,GCG	A49A	NP_064594.3

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