Product Details

SNP ID

rs184815636

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.15:56631784 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AATGCTTACATTATCTGATGCTAAT[C/T]GCAAATCCTTAATATTCTTTGAAGA

Phenotype

Polymorphism

C/T, Transition 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	2513	Missense Mutation	CAA,CGA	Q872R	NP_001002843.1
NM_001002844.2	2513	Intron			NP_001002844.1
NM_001288588.1	2513	Missense Mutation	CAA,CGA	Q885R	NP_001275517.1
NM_001288589.1	2513	Intron			NP_001275518.1
NM_017661.3	2513	Missense Mutation	CAA,CGA	Q885R	NP_060131.2
XM_005254481.3	2513	Intron			XP_005254538.2
XM_005254483.3	2513	Intron			XP_005254540.2
XM_005254484.3	2513	Intron			XP_005254541.2
XM_005254485.3	2513	Intron			XP_005254542.2
XM_011521701.1	2513	Missense Mutation	CAA,CGA	Q820R	XP_011520003.1
XM_011521702.1	2513	Missense Mutation	CAA,CGA	Q885R	XP_011520004.1
XM_011521704.2	2513	Intron			XP_011520006.1
XM_011521707.2	2513	Intron			XP_011520009.1
XM_011521708.1	2513	Missense Mutation	CAA,CGA	Q779R	XP_011520010.1
XM_011521709.1	2513	Missense Mutation	CAA,CGA	Q779R	XP_011520011.1
XM_011521710.1	2513	Missense Mutation	CAA,CGA	Q779R	XP_011520012.1
XM_011521711.1	2513	Intron			XP_011520013.1
XM_017022344.1	2513	Missense Mutation	CAA,CGA	Q885R	XP_016877833.1
XM_017022345.1	2513	Missense Mutation	CAA,CGA	Q885R	XP_016877834.1
XM_017022346.1	2513	Intron			XP_016877835.1
XM_017022347.1	2513	Intron			XP_016877836.1
XM_017022348.1	2513	Intron			XP_016877837.1
XM_017022349.1	2513	Missense Mutation	CAA,CGA	Q397R	XP_016877838.1

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