Product Details

SNP ID

rs201934688

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.4:499420 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CGCGGTCTTCCTTCGGGGATTCTTC[C/G]CGGCTCCCGTTCGTTCCTCTGCCAG

Phenotype

MIM: 616918

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

PIGG PubMed Links

Gene Details

Gene

PIGG

Gene Name

phosphatidylinositol glycan anchor biosynthesis class G

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001127178.2	219	Missense Mutation	CCG,GCG	P29A	NP_001120650.1
NM_001289051.1	219	Intron			NP_001275980.1
NM_001289052.1	219	Missense Mutation	CCG,GCG	P29A	NP_001275981.1
NM_001289053.1	219	UTR 5			NP_001275982.1
NM_001289055.1	219	UTR 5			NP_001275984.1
NM_001289057.1	219	UTR 5			NP_001275986.1
NM_017733.4	219	Missense Mutation	CCG,GCG	P29A	NP_060203.3
XM_005272284.2	219	UTR 5			XP_005272341.1
XM_011513490.2	219	Missense Mutation	CCG,GCG	P29A	XP_011511792.1
XM_011513491.1	219	UTR 5			XP_011511793.1
XM_011513492.1	219	Intron			XP_011511794.1
XM_011513493.1	219	Missense Mutation	CCG,GCG	P29A	XP_011511795.1
XM_011513494.2	219	Missense Mutation	CCG,GCG	P29A	XP_011511796.1
XM_017008321.1	219	UTR 5			XP_016863810.1
XM_017008322.1	219	UTR 5			XP_016863811.1
XM_017008323.1	219	UTR 5			XP_016863812.1
XM_017008324.1	219	UTR 5			XP_016863813.1
XM_017008325.1	219	UTR 5			XP_016863814.1
XM_017008326.1	219	Missense Mutation	CCG,GCG	P29A	XP_016863815.1

Gene

ZNF721

Gene Name

zinc finger protein 721

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_133474.3	219	Intron			NP_597731.2

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