Product Details

SNP ID

rs150967731

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.6:28995953 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGGCTTCTCCCCGGTGTGGATAAGC[C/T]GATGCATACAGAGACGGTTCCTGGT

Phenotype

Polymorphism

C/T, 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	1512	Missense Mutation	CAG,CGG	Q350R	NP_001010877.2
NM_001318534.1	1512	Missense Mutation	CAG,CGG	Q258R	NP_001305463.1
NM_001318535.1	1512	Missense Mutation	CAG,CGG	Q258R	NP_001305464.1
XM_005249019.3	1512	Missense Mutation	CAG,CGG	Q383R	XP_005249076.1
XM_006715067.2	1512	Missense Mutation	CAG,CGG	Q383R	XP_006715130.1
XM_011514510.1	1512	Missense Mutation	CAG,CGG	Q383R	XP_011512812.1
XM_011514511.2	1512	Missense Mutation	CAG,CGG	Q383R	XP_011512813.1
XM_011514512.1	1512	Missense Mutation	CAG,CGG	Q375R	XP_011512814.1
XM_011514513.1	1512	Missense Mutation	CAG,CGG	Q374R	XP_011512815.1
XM_011514514.1	1512	Missense Mutation	CAG,CGG	Q358R	XP_011512816.1
XM_011514516.1	1512	Missense Mutation	CAG,CGG	Q302R	XP_011512818.1
XM_011514517.1	1512	Missense Mutation	CAG,CGG	Q258R	XP_011512819.1
XM_011514518.1	1512	Missense Mutation	CAG,CGG	Q258R	XP_011512820.1
XM_017010756.1	1512	Missense Mutation	CAG,CGG	Q383R	XP_016866245.1
XM_017010757.1	1512	Missense Mutation	CAG,CGG	Q383R	XP_016866246.1
XM_017010758.1	1512	Missense Mutation	CAG,CGG	Q350R	XP_016866247.1
XM_017010759.1	1512	Missense Mutation	CAG,CGG	Q350R	XP_016866248.1
XM_017010760.1	1512	Missense Mutation	CAG,CGG	Q302R	XP_016866249.1
XM_017010761.1	1512	Missense Mutation	CAG,CGG	Q258R	XP_016866250.1

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