Product Details

SNP ID

rs199895235

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.15:56631998 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTTGAGCCAGTTTCCTGGTCTGCAA[C/G]ACAGGTTTCATTTTCCTTATCTGAA

Phenotype

Polymorphism

C/G, 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	2299	Missense Mutation	CTT,GTT	L801V	NP_001002843.1
NM_001002844.2	2299	Intron			NP_001002844.1
NM_001288588.1	2299	Missense Mutation	CTT,GTT	L814V	NP_001275517.1
NM_001288589.1	2299	Intron			NP_001275518.1
NM_017661.3	2299	Missense Mutation	CTT,GTT	L814V	NP_060131.2
XM_005254481.3	2299	Intron			XP_005254538.2
XM_005254483.3	2299	Intron			XP_005254540.2
XM_005254484.3	2299	Intron			XP_005254541.2
XM_005254485.3	2299	Intron			XP_005254542.2
XM_011521701.1	2299	Missense Mutation	CTT,GTT	L749V	XP_011520003.1
XM_011521702.1	2299	Missense Mutation	CTT,GTT	L814V	XP_011520004.1
XM_011521704.2	2299	Intron			XP_011520006.1
XM_011521707.2	2299	Intron			XP_011520009.1
XM_011521708.1	2299	Missense Mutation	CTT,GTT	L708V	XP_011520010.1
XM_011521709.1	2299	Missense Mutation	CTT,GTT	L708V	XP_011520011.1
XM_011521710.1	2299	Missense Mutation	CTT,GTT	L708V	XP_011520012.1
XM_011521711.1	2299	Intron			XP_011520013.1
XM_017022344.1	2299	Missense Mutation	CTT,GTT	L814V	XP_016877833.1
XM_017022345.1	2299	Missense Mutation	CTT,GTT	L814V	XP_016877834.1
XM_017022346.1	2299	Intron			XP_016877835.1
XM_017022347.1	2299	Intron			XP_016877836.1
XM_017022348.1	2299	Intron			XP_016877837.1
XM_017022349.1	2299	Missense Mutation	CTT,GTT	L326V	XP_016877838.1

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