Product Details

SNP ID

rs61741526

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.15:56631697 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGTCAGAGGTTCCAAATGAATACTG[A/C]CTTGCTCGCTAACATCAGAACTAAC

Phenotype

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

ZNF280D PubMed Links

Gene Details

Gene

ZNF280D

Gene Name

zinc finger protein 280D

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001002843.2	2600	Missense Mutation	GGC,GTC	G901V	NP_001002843.1
NM_001002844.2	2600	Intron			NP_001002844.1
NM_001288588.1	2600	Missense Mutation	GGC,GTC	G914V	NP_001275517.1
NM_001288589.1	2600	Intron			NP_001275518.1
NM_017661.3	2600	Missense Mutation	GGC,GTC	G914V	NP_060131.2
XM_005254481.3	2600	Intron			XP_005254538.2
XM_005254483.3	2600	Intron			XP_005254540.2
XM_005254484.3	2600	Intron			XP_005254541.2
XM_005254485.3	2600	Intron			XP_005254542.2
XM_011521701.1	2600	Missense Mutation	GGC,GTC	G849V	XP_011520003.1
XM_011521702.1	2600	Missense Mutation	GGC,GTC	G914V	XP_011520004.1
XM_011521704.2	2600	Intron			XP_011520006.1
XM_011521707.2	2600	Intron			XP_011520009.1
XM_011521708.1	2600	Missense Mutation	GGC,GTC	G808V	XP_011520010.1
XM_011521709.1	2600	Missense Mutation	GGC,GTC	G808V	XP_011520011.1
XM_011521710.1	2600	Missense Mutation	GGC,GTC	G808V	XP_011520012.1
XM_011521711.1	2600	Intron			XP_011520013.1
XM_017022344.1	2600	Missense Mutation	GGC,GTC	G914V	XP_016877833.1
XM_017022345.1	2600	Missense Mutation	GGC,GTC	G914V	XP_016877834.1
XM_017022346.1	2600	Intron			XP_016877835.1
XM_017022347.1	2600	Intron			XP_016877836.1
XM_017022348.1	2600	Intron			XP_016877837.1
XM_017022349.1	2600	Missense Mutation	GGC,GTC	G426V	XP_016877838.1

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