Product Details

SNP ID

rs5745907

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.15:75349311 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AAAGTGGCAGCCGGGCCGCGGGCCC[C/T]GTGTCTTGCAGGAGTACCAGCAGTT

Phenotype

MIM: 616701 MIM: 154580 MIM: 608844

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

COMMD4 PubMed Links

Gene Details

Gene

COMMD4

Gene Name

COMM domain containing 4

There are no transcripts associated with this gene.

Gene

MAN2C1

Gene Name

mannosidase alpha class 2C member 1

There are no transcripts associated with this gene.

Gene

MIR631

Gene Name

microRNA 631

There are no transcripts associated with this gene.

Gene

NEIL1

Gene Name

nei like DNA glycosylase 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001256552.1	831	Missense Mutation	CGT,TGT	R222C	NP_001243481.1
NM_024608.3	831	Missense Mutation	CGT,TGT	R136C	NP_078884.2
XM_005254659.4	831	Missense Mutation	CGT,TGT	R136C	XP_005254716.1
XM_006720677.3	831	Missense Mutation	CGT,TGT	R213C	XP_006720740.1
XM_006720678.3	831	Missense Mutation	CGT,TGT	R222C	XP_006720741.1
XM_006720679.3	831	Missense Mutation	CGT,TGT	R179C	XP_006720742.1
XM_006720680.1	831	Missense Mutation	CGT,TGT	R136C	XP_006720743.1
XM_006720681.1	831	Missense Mutation	CGT,TGT	R136C	XP_006720744.1
XM_011522001.2	831	Missense Mutation	CGT,TGT	R199C	XP_011520303.2
XM_011522002.1	831	Missense Mutation	CGT,TGT	R136C	XP_011520304.1
XM_011522003.2	831	Missense Mutation	CGT,TGT	R136C	XP_011520305.1
XM_011522004.2	831	Missense Mutation	CGT,TGT	R136C	XP_011520306.1
XM_011522005.1	831	Missense Mutation	CCG,CTG	P24L	XP_011520307.1
XM_011522006.1	831	Silent Mutation	CCC,CCT	P40P	XP_011520308.1
XM_011522007.1	831	Silent Mutation	CCC,CCT	P40P	XP_011520309.1
XM_011522008.1	831	Silent Mutation	CCC,CCT	P40P	XP_011520310.1
XM_017022566.1	831	Missense Mutation	CGT,TGT	R213C	XP_016878055.1
XM_017022567.1	831	Silent Mutation	CCC,CCT	P40P	XP_016878056.1
XM_017022568.1	831	Missense Mutation	CGT,TGT	R222C	XP_016878057.1

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