Product Details

SNP ID
rs145518709
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.4:127921539 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCTGGCTTACCTGAGGTTTTGGTCC[C/T]AGAATTTTTGAATATAGAGTATAGG
Phenotype
MIM: 611124
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
MFSD8 PubMed Links

Gene Details

Gene
MFSD8
Gene Name
major facilitator superfamily domain containing 8
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_152778.2 1308 Silent Mutation CTA,CTG L445L NP_689991.1
XM_005262893.1 1308 Silent Mutation CTA,CTG L445L XP_005262950.1
XM_005262896.1 1308 Silent Mutation CTA,CTG L396L XP_005262953.1
XM_005262897.2 1308 Silent Mutation CTA,CTG L378L XP_005262954.1
XM_005262898.2 1308 UTR 3 XP_005262955.1
XM_011531830.1 1308 Silent Mutation CTA,CTG L407L XP_011530132.1
XM_011531831.1 1308 Silent Mutation CTA,CTG L340L XP_011530133.1
XM_011531832.1 1308 UTR 3 XP_011530134.1
XM_017007989.1 1308 UTR 3 XP_016863478.1

View Full Product Details