Product Details

SNP ID

rs114790937

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.18:24430352 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTTGGCTTAAAGGGCAAGAACGTGC[A/G]GATTTATCAAATAGCCTTGAGGAAA

Phenotype

MIM: 615319

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

IMPACT PubMed Links

Gene Details

Gene

IMPACT

Gene Name

impact RWD domain protein

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_018439.3	361	Silent Mutation	GCA,GCG	A83A	NP_060909.1
XM_017025832.1	361	Silent Mutation	GCA,GCG	A65A	XP_016881321.1

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