Product Details

SNP ID
rs17504209
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.6:87513998 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
ATAACTTGACAAGTCACATTTAATA[C/T]AGATTCTGACACAGAATAATAGTTT
Phenotype
MIM: 611524 MIM: 605634
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
RARS2 PubMed Links

Gene Details

Gene
RARS2
Gene Name
arginyl-tRNA synthetase 2, mitochondrial
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001318785.1 2392 UTR 3 NP_001305714.1
NM_020320.4 2392 UTR 3 NP_064716.2
XM_011535948.2 2392 UTR 3 XP_011534250.1
XM_011535949.2 2392 Intron XP_011534251.1
XM_017011072.1 2392 UTR 3 XP_016866561.1
XM_017011073.1 2392 UTR 3 XP_016866562.1
XM_017011074.1 2392 UTR 3 XP_016866563.1
XM_017011075.1 2392 UTR 3 XP_016866564.1
XM_017011076.1 2392 UTR 3 XP_016866565.1
XM_017011077.1 2392 UTR 3 XP_016866566.1
XM_017011078.1 2392 Intron XP_016866567.1
XM_017011079.1 2392 UTR 3 XP_016866568.1
XM_017011080.1 2392 Intron XP_016866569.1
XM_017011081.1 2392 Intron XP_016866570.1
Gene
SLC35A1
Gene Name
solute carrier family 35 member A1
There are no transcripts associated with this gene.

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