Product Details

SNP ID

rs190540164

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.15:56631812 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AAATCCTTAATATTCTTTGAAGAAA[A/G]TCTGGCTTCACTGGAGTTGTGATCT

Phenotype

Polymorphism

A/G, 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	2485	Missense Mutation	CTT,TTT	L863F	NP_001002843.1
NM_001002844.2	2485	Intron			NP_001002844.1
NM_001288588.1	2485	Missense Mutation	CTT,TTT	L876F	NP_001275517.1
NM_001288589.1	2485	Intron			NP_001275518.1
NM_017661.3	2485	Missense Mutation	CTT,TTT	L876F	NP_060131.2
XM_005254481.3	2485	Intron			XP_005254538.2
XM_005254483.3	2485	Intron			XP_005254540.2
XM_005254484.3	2485	Intron			XP_005254541.2
XM_005254485.3	2485	Intron			XP_005254542.2
XM_011521701.1	2485	Missense Mutation	CTT,TTT	L811F	XP_011520003.1
XM_011521702.1	2485	Missense Mutation	CTT,TTT	L876F	XP_011520004.1
XM_011521704.2	2485	Intron			XP_011520006.1
XM_011521707.2	2485	Intron			XP_011520009.1
XM_011521708.1	2485	Missense Mutation	CTT,TTT	L770F	XP_011520010.1
XM_011521709.1	2485	Missense Mutation	CTT,TTT	L770F	XP_011520011.1
XM_011521710.1	2485	Missense Mutation	CTT,TTT	L770F	XP_011520012.1
XM_011521711.1	2485	Intron			XP_011520013.1
XM_017022344.1	2485	Missense Mutation	CTT,TTT	L876F	XP_016877833.1
XM_017022345.1	2485	Missense Mutation	CTT,TTT	L876F	XP_016877834.1
XM_017022346.1	2485	Intron			XP_016877835.1
XM_017022347.1	2485	Intron			XP_016877836.1
XM_017022348.1	2485	Intron			XP_016877837.1
XM_017022349.1	2485	Missense Mutation	CTT,TTT	L388F	XP_016877838.1

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