Product Details

SNP ID

rs7108281

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:65376522 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GAAGAAGACTCCCAGTCCTTCCTGC[C/T]GGATGCTGCTCACCATGCAGTCCAG

Phenotype

MIM: 610825

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

SLC25A45 PubMed Links

Gene Details

Gene

SLC25A45

Gene Name

solute carrier family 25 member 45

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001077241.2	1761	Missense Mutation	CAG,CGG	Q209R	NP_001070709.2
NM_001278250.2	1761	Missense Mutation	CAG,CGG	Q227R	NP_001265179.2
NM_001278251.2	1761	Missense Mutation	CAG,CGG	Q209R	NP_001265180.2
NM_001300820.1	1761	Missense Mutation	CAG,CGG	Q189R	NP_001287749.1
NM_182556.3	1761	Missense Mutation	CAG,CGG	Q251R	NP_872362.3
XM_006718509.3	1761	Missense Mutation	CAG,CGG	Q209R	XP_006718572.1
XM_006718510.3	1761	Missense Mutation	CAG,CGG	Q209R	XP_006718573.1
XM_011544943.2	1761	Missense Mutation	CAG,CGG	Q209R	XP_011543245.1
XM_011544944.2	1761	Missense Mutation	CAG,CGG	Q209R	XP_011543246.1
XM_011544947.2	1761	Intron			XP_011543249.1
XM_011544949.2	1761	Missense Mutation	CAG,CGG	Q209R	XP_011543251.1
XM_017017562.1	1761	Intron			XP_016873051.1
XM_017017563.1	1761	Missense Mutation	CAG,CGG	Q209R	XP_016873052.1
XM_017017564.1	1761	Missense Mutation	CAG,CGG	Q209R	XP_016873053.1
XM_017017565.1	1761	Missense Mutation	CAG,CGG	Q209R	XP_016873054.1
XM_017017566.1	1761	Missense Mutation	CAG,CGG	Q209R	XP_016873055.1
XM_017017567.1	1761	Missense Mutation	CAG,CGG	Q209R	XP_016873056.1
XM_017017568.1	1761	Missense Mutation	CAG,CGG	Q209R	XP_016873057.1
XM_017017569.1	1761	Missense Mutation	CAG,CGG	Q209R	XP_016873058.1
XM_017017570.1	1761	Missense Mutation	CAG,CGG	Q147R	XP_016873059.1
XM_017017571.1	1761	Missense Mutation	CAG,CGG	Q147R	XP_016873060.1

View Full Product Details