Product Details

SNP ID

rs8177879

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.16:81089766 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TCATTTTCTCTTAAACAGTATCGCC[A/G]TATGGAATTGAGGGGAATTTACAGA

Phenotype

MIM: 238330

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

GCSH PubMed Links

Gene Details

Gene

GCSH

Gene Name

glycine cleavage system protein H

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_004483.4		Intron			NP_004474.2
XM_017023136.1		Intron			XP_016878625.1
XM_017023137.1		Intron			XP_016878626.1

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