Product Details

SNP ID

rs117764534

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.15:56631916 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CATTTCCTGACAAACGTGTTGTATT[G/T]GTTTTTTCTTTTCCACTTTATCTGC

Phenotype

Polymorphism

G/T, 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	2381	Missense Mutation	CAA,CCA	Q828P	NP_001002843.1
NM_001002844.2	2381	Intron			NP_001002844.1
NM_001288588.1	2381	Missense Mutation	CAA,CCA	Q841P	NP_001275517.1
NM_001288589.1	2381	Intron			NP_001275518.1
NM_017661.3	2381	Missense Mutation	CAA,CCA	Q841P	NP_060131.2
XM_005254481.3	2381	Intron			XP_005254538.2
XM_005254483.3	2381	Intron			XP_005254540.2
XM_005254484.3	2381	Intron			XP_005254541.2
XM_005254485.3	2381	Intron			XP_005254542.2
XM_011521701.1	2381	Missense Mutation	CAA,CCA	Q776P	XP_011520003.1
XM_011521702.1	2381	Missense Mutation	CAA,CCA	Q841P	XP_011520004.1
XM_011521704.2	2381	Intron			XP_011520006.1
XM_011521707.2	2381	Intron			XP_011520009.1
XM_011521708.1	2381	Missense Mutation	CAA,CCA	Q735P	XP_011520010.1
XM_011521709.1	2381	Missense Mutation	CAA,CCA	Q735P	XP_011520011.1
XM_011521710.1	2381	Missense Mutation	CAA,CCA	Q735P	XP_011520012.1
XM_011521711.1	2381	Intron			XP_011520013.1
XM_017022344.1	2381	Missense Mutation	CAA,CCA	Q841P	XP_016877833.1
XM_017022345.1	2381	Missense Mutation	CAA,CCA	Q841P	XP_016877834.1
XM_017022346.1	2381	Intron			XP_016877835.1
XM_017022347.1	2381	Intron			XP_016877836.1
XM_017022348.1	2381	Intron			XP_016877837.1
XM_017022349.1	2381	Missense Mutation	CAA,CCA	Q353P	XP_016877838.1

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