Product Details

SNP ID

rs1803791

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.14:100337144 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGACACGTCCACATCACAGTTGCCC[A/C]CAAACTGCCTGTGCTCCTCGATGGT

Phenotype

MIM: 609911 MIM: 191050

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

SLC25A47 PubMed Links

Gene Details

Gene

SLC25A47

Gene Name

solute carrier family 25 member 47

There are no transcripts associated with this gene.

Gene

WARS

Gene Name

tryptophanyl-tRNA synthetase

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_004184.3	1527	Missense Mutation	GGG,GTG	G391V	NP_004175.2
NM_173701.1	1527	Missense Mutation	GGG,GTG	G391V	NP_776049.1
NM_213645.1	1527	Missense Mutation	GGG,GTG	G350V	NP_998810.1
NM_213646.1	1527	Missense Mutation	GGG,GTG	G350V	NP_998811.1
XM_005268044.3	1527	Missense Mutation	GGG,GTG	G391V	XP_005268101.1
XM_006720249.3	1527	Missense Mutation	GGG,GTG	G391V	XP_006720312.1
XM_011537133.2	1527	Missense Mutation	GGG,GTG	G391V	XP_011535435.1
XM_011537135.2	1527	Missense Mutation	GGG,GTG	G391V	XP_011535437.1
XM_011537136.2	1527	Missense Mutation	GGG,GTG	G350V	XP_011535438.1
XM_017021627.1	1527	Missense Mutation	GGG,GTG	G391V	XP_016877116.1
XM_017021628.1	1527	Missense Mutation	GGG,GTG	G391V	XP_016877117.1
XM_017021629.1	1527	Missense Mutation	GGG,GTG	G391V	XP_016877118.1

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