Product Details

SNP ID

rs1049402

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.7:30595045 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

CCGGTCCCTCAGCGCGGCCTCCTGC[C/G]CCCCGATCTCCTTGCCCGCCGCCGC

Phenotype

MIM: 600287

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

GARS PubMed Links

Gene Details

Gene

GARS

Gene Name

glycyl-tRNA synthetase

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001316772.1	311	UTR 5			NP_001303701.1
NM_002047.3	311	Missense Mutation	CCC,GCC	P42A	NP_002038.2
XM_006715686.2	311	UTR 5			XP_006715749.1

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