Product Details

SNP ID

rs202210528

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.13:91399126 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GTTGGGTCCGCCCGCAGCGAGGGCG[A/T]GCAGACCTGCGAAGAAGTTCGGAAA

Phenotype

MIM: 602446

Polymorphism

A/T, Transversion substitution

Allele Nomenclature

Literature Links

GPC5 PubMed Links

Gene Details

Gene

GPC5

Gene Name

glypican 5

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_004466.5	440	Missense Mutation	GAG,GTG	E27V	NP_004457.1
XM_011521054.2	440	Missense Mutation	GAG,GTG	E27V	XP_011519356.1
XM_011521055.2	440	Missense Mutation	GAG,GTG	E27V	XP_011519357.1
XM_011521056.2	440	Missense Mutation	GAG,GTG	E27V	XP_011519358.1
XM_011521057.2	440	Missense Mutation	GAG,GTG	E27V	XP_011519359.1
XM_011521058.2	440	Missense Mutation	GAG,GTG	E27V	XP_011519360.1
XM_011521059.2	440	Missense Mutation	GAG,GTG	E27V	XP_011519361.1
XM_011521060.2	440	Missense Mutation	GAG,GTG	E27V	XP_011519362.1
XM_017020435.1	440	Missense Mutation	GAG,GTG	E27V	XP_016875924.1
XM_017020436.1	440	Missense Mutation	GAG,GTG	E27V	XP_016875925.1
XM_017020437.1	440	Missense Mutation	GAG,GTG	E27V	XP_016875926.1

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