Product Details

SNP ID

rs141915692

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.10:75094696 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCAGATCAGAACCGCCCCGTCTCCC[A/G]CCCCAGTCGGTTGTCCAGAACCTGG

Phenotype

MIM: 613191 MIM: 611575

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

DUSP13 PubMed Links

Gene Details

Gene

DUSP13

Gene Name

dual specificity phosphatase 13

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001007271.1	1081	UTR 3			NP_001007272.1
NM_001007272.1	1081	Missense Mutation	CGG,TGG	R243W	NP_001007273.1
NM_001007273.1	1081	Missense Mutation	CGG,TGG	R286W	NP_001007274.1
NM_001320842.1	1081	Missense Mutation	CGG,TGG	R286W	NP_001307771.1
NM_001320843.1	1081	Missense Mutation	CGG,TGG	R193W	NP_001307772.1
NM_016364.3	1081	Missense Mutation	CGG,TGG	R193W	NP_057448.3
XM_005269883.3	1081	Missense Mutation	CGG,TGG	R412W	XP_005269940.1
XM_005269884.4	1081	Missense Mutation	CGG,TGG	R329W	XP_005269941.3
XM_005269887.1	1081	Missense Mutation	CGG,TGG	R286W	XP_005269944.1
XM_005269890.1	1081	Missense Mutation	CGG,TGG	R193W	XP_005269947.1
XM_011539853.1	1081	Missense Mutation	CGG,TGG	R322W	XP_011538155.1
XM_011539854.2	1081	Missense Mutation	CGG,TGG	R193W	XP_011538156.1
XM_011539855.1	1081	Missense Mutation	CGG,TGG	R193W	XP_011538157.1
XM_011539856.2	1081	Missense Mutation	CGG,TGG	R193W	XP_011538158.1
XM_017016313.1	1081	Missense Mutation	CGG,TGG	R241W	XP_016871802.1
XM_017016314.1	1081	Intron			XP_016871803.1

Gene

SAMD8

Gene Name

sterile alpha motif domain containing 8

There are no transcripts associated with this gene.

View Full Product Details