Product Details

SNP ID

rs140431320

Assay Type

Functionally tested

NCBI dbSNP Submissions

1

Location

Chr.1:108974543 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GAAGTCGATCTCAATCACCTTGTAG[A/G]TCTGTCACCTTTATTTTCATATCAT

Phenotype

MIM: 615734

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

WDR47 PubMed Links

Gene Details

Gene

WDR47

Gene Name

WD repeat domain 47

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001142550.1	2984	Silent Mutation	GAC,GAT	D878D	NP_001136022.1
NM_001142551.1	2984	Silent Mutation	GAC,GAT	D870D	NP_001136023.1
NM_014969.5	2984	Silent Mutation	GAC,GAT	D871D	NP_055784.3
XM_006710460.3	2984	Silent Mutation	GAC,GAT	D873D	XP_006710523.1
XM_011541027.2	2984	Silent Mutation	GAC,GAT	D879D	XP_011539329.1
XM_011541028.2	2984	Silent Mutation	GAC,GAT	D872D	XP_011539330.1
XM_011541029.1	2984	Silent Mutation	GAC,GAT	D880D	XP_011539331.1
XM_011541030.1	2984	Silent Mutation	GAC,GAT	D873D	XP_011539332.1
XM_011541031.1	2984	Silent Mutation	GAC,GAT	D780D	XP_011539333.1
XM_017000696.1	2984	Silent Mutation	GAC,GAT	D877D	XP_016856185.1
XM_017000697.1	2984	Silent Mutation	GAC,GAT	D870D	XP_016856186.1

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