Product Details

SNP ID

rs138592266

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.10:102469149 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCTTCCTGCTCTACTATGTGGACAC[C/T]TTTGTCTCAGTGTACAAGATCAACA

Phenotype

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

MFSD13A PubMed Links

Gene Details

Gene

MFSD13A

Gene Name

major facilitator superfamily domain containing 13A

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_024789.3	962	Silent Mutation	ACC,ACT	T40T	NP_079065.2
XM_006717973.3	962	Silent Mutation	ACC,ACT	T40T	XP_006718036.1
XM_006717974.3	962	Silent Mutation	ACC,ACT	T40T	XP_006718037.1
XM_011540160.2	962	Silent Mutation	ACC,ACT	T40T	XP_011538462.1
XM_011540163.2	962	Silent Mutation	ACC,ACT	T40T	XP_011538465.1
XM_011540167.2	962	Silent Mutation	ACC,ACT	T40T	XP_011538469.1
XM_011540169.2	962	Silent Mutation	ACC,ACT	T40T	XP_011538471.1
XM_017016654.1	962	Silent Mutation	ACC,ACT	T40T	XP_016872143.1
XM_017016655.1	962	Silent Mutation	ACC,ACT	T40T	XP_016872144.1
XM_017016656.1	962	Silent Mutation	ACC,ACT	T40T	XP_016872145.1
XM_017016657.1	962	Silent Mutation	ACC,ACT	T40T	XP_016872146.1
XM_017016658.1	962	Silent Mutation	ACC,ACT	T40T	XP_016872147.1
XM_017016659.1	962	Silent Mutation	ACC,ACT	T40T	XP_016872148.1
XM_017016660.1	962	Intron			XP_016872149.1
XM_017016661.1	962	Silent Mutation	ACC,ACT	T40T	XP_016872150.1
XM_017016662.1	962	Silent Mutation	ACC,ACT	T40T	XP_016872151.1

View Full Product Details