Product Details

SNP ID

rs199702171

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.15:56631502 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGAAACTTAAAATGACTAATTTCAA[C/T]TTCTTTCTTTTTCGTCTTCCAGGTC

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	2795	Missense Mutation	AAT,AGT	N966S	NP_001002843.1
NM_001002844.2	2795	Intron			NP_001002844.1
NM_001288588.1	2795	Missense Mutation	AAT,AGT	N979S	NP_001275517.1
NM_001288589.1	2795	Intron			NP_001275518.1
NM_017661.3	2795	Missense Mutation	AAT,AGT	N979S	NP_060131.2
XM_005254481.3	2795	Intron			XP_005254538.2
XM_005254483.3	2795	Intron			XP_005254540.2
XM_005254484.3	2795	Intron			XP_005254541.2
XM_005254485.3	2795	Intron			XP_005254542.2
XM_011521701.1	2795	Missense Mutation	AAT,AGT	N914S	XP_011520003.1
XM_011521702.1	2795	Missense Mutation	AAT,AGT	N979S	XP_011520004.1
XM_011521704.2	2795	Intron			XP_011520006.1
XM_011521707.2	2795	Intron			XP_011520009.1
XM_011521708.1	2795	Missense Mutation	AAT,AGT	N873S	XP_011520010.1
XM_011521709.1	2795	Missense Mutation	AAT,AGT	N873S	XP_011520011.1
XM_011521710.1	2795	Missense Mutation	AAT,AGT	N873S	XP_011520012.1
XM_011521711.1	2795	Intron			XP_011520013.1
XM_017022344.1	2795	Missense Mutation	AAT,AGT	N979S	XP_016877833.1
XM_017022345.1	2795	Missense Mutation	AAT,AGT	N979S	XP_016877834.1
XM_017022346.1	2795	Intron			XP_016877835.1
XM_017022347.1	2795	Intron			XP_016877836.1
XM_017022348.1	2795	Intron			XP_016877837.1
XM_017022349.1	2795	Missense Mutation	AAT,AGT	N491S	XP_016877838.1

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