Product Details

SNP ID

rs202001840

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.15:72163398 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGGAGAGCAGTTCGGCATCTTCTTA[C/G]GGCAGGCAGGACCCCAGCCTGGCAT

Phenotype

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

GRAMD2 PubMed Links

Gene Details

Gene

GRAMD2

Gene Name

GRAM domain containing 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001012642.2	1032	Missense Mutation	CCT,CGT	P275R	NP_001012660.1
XM_011521327.2	1032	Missense Mutation	CCT,CGT	P274R	XP_011519629.1
XM_011521328.2	1032	Missense Mutation	CCT,CGT	P273R	XP_011519630.1
XM_011521329.2	1032	Missense Mutation	CCT,CGT	P265R	XP_011519631.1
XM_011521330.2	1032	Missense Mutation	CCT,CGT	P263R	XP_011519632.1
XM_011521331.2	1032	Missense Mutation	CCT,CGT	P256R	XP_011519633.1
XM_011521332.2	1032	Missense Mutation	CCT,CGT	P239R	XP_011519634.1
XM_011521333.2	1032	Missense Mutation	CCT,CGT	P239R	XP_011519635.1
XM_017021997.1	1032	Missense Mutation	CCT,CGT	P237R	XP_016877486.1
XM_017021998.1	1032	Missense Mutation	CCT,CGT	P237R	XP_016877487.1

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