Product Details

SNP ID

rs9295783

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.6:28995546 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GTATGCTCTCGTTCATGAGCCCTGC[A/G]CTTACAGTTATGACGAAAGGCTTTC

Phenotype

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

HCG16 PubMed Links

Gene Details

Gene

HCG16

Gene Name

HLA complex group 16 (non-protein coding)

There are no transcripts associated with this gene.

Gene

ZNF311

Gene Name

zinc finger protein 311

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001010877.3	1919	Missense Mutation	CGC,TGC	R486C	NP_001010877.2
NM_001318534.1	1919	Missense Mutation	CGC,TGC	R394C	NP_001305463.1
NM_001318535.1	1919	Missense Mutation	CGC,TGC	R394C	NP_001305464.1
XM_005249019.3	1919	Missense Mutation	CGC,TGC	R519C	XP_005249076.1
XM_006715067.2	1919	Missense Mutation	CGC,TGC	R519C	XP_006715130.1
XM_011514510.1	1919	Missense Mutation	CGC,TGC	R519C	XP_011512812.1
XM_011514511.2	1919	Missense Mutation	CGC,TGC	R519C	XP_011512813.1
XM_011514512.1	1919	Missense Mutation	CGC,TGC	R511C	XP_011512814.1
XM_011514513.1	1919	Missense Mutation	CGC,TGC	R510C	XP_011512815.1
XM_011514514.1	1919	Missense Mutation	CGC,TGC	R494C	XP_011512816.1
XM_011514516.1	1919	Missense Mutation	CGC,TGC	R438C	XP_011512818.1
XM_011514517.1	1919	Missense Mutation	CGC,TGC	R394C	XP_011512819.1
XM_011514518.1	1919	Missense Mutation	CGC,TGC	R394C	XP_011512820.1
XM_017010756.1	1919	Missense Mutation	CGC,TGC	R519C	XP_016866245.1
XM_017010757.1	1919	Missense Mutation	CGC,TGC	R519C	XP_016866246.1
XM_017010758.1	1919	Missense Mutation	CGC,TGC	R486C	XP_016866247.1
XM_017010759.1	1919	Missense Mutation	CGC,TGC	R486C	XP_016866248.1
XM_017010760.1	1919	Missense Mutation	CGC,TGC	R438C	XP_016866249.1
XM_017010761.1	1919	Missense Mutation	CGC,TGC	R394C	XP_016866250.1

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