Product Details

SNP ID

rs145687726

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.6:28995693 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CACCCATAGTGTTTCTCCCGAGTAT[G/T]GATTCGTTTGTGTTTGCTTAGGTCT

Phenotype

Polymorphism

G/T, Transversion 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	1772	Missense Mutation	AAT,CAT	N437H	NP_001010877.2
NM_001318534.1	1772	Missense Mutation	AAT,CAT	N345H	NP_001305463.1
NM_001318535.1	1772	Missense Mutation	AAT,CAT	N345H	NP_001305464.1
XM_005249019.3	1772	Missense Mutation	AAT,CAT	N470H	XP_005249076.1
XM_006715067.2	1772	Missense Mutation	AAT,CAT	N470H	XP_006715130.1
XM_011514510.1	1772	Missense Mutation	AAT,CAT	N470H	XP_011512812.1
XM_011514511.2	1772	Missense Mutation	AAT,CAT	N470H	XP_011512813.1
XM_011514512.1	1772	Missense Mutation	AAT,CAT	N462H	XP_011512814.1
XM_011514513.1	1772	Missense Mutation	AAT,CAT	N461H	XP_011512815.1
XM_011514514.1	1772	Missense Mutation	AAT,CAT	N445H	XP_011512816.1
XM_011514516.1	1772	Missense Mutation	AAT,CAT	N389H	XP_011512818.1
XM_011514517.1	1772	Missense Mutation	AAT,CAT	N345H	XP_011512819.1
XM_011514518.1	1772	Missense Mutation	AAT,CAT	N345H	XP_011512820.1
XM_017010756.1	1772	Missense Mutation	AAT,CAT	N470H	XP_016866245.1
XM_017010757.1	1772	Missense Mutation	AAT,CAT	N470H	XP_016866246.1
XM_017010758.1	1772	Missense Mutation	AAT,CAT	N437H	XP_016866247.1
XM_017010759.1	1772	Missense Mutation	AAT,CAT	N437H	XP_016866248.1
XM_017010760.1	1772	Missense Mutation	AAT,CAT	N389H	XP_016866249.1
XM_017010761.1	1772	Missense Mutation	AAT,CAT	N345H	XP_016866250.1

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