Product Details

SNP ID
rs11938181
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.4:127918225 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CTCCTGTTGTCATTTTCTCTTTATA[C/T]GCAACTTGGCCTACTCAAGAAGACA
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 4622 UTR 3 NP_689991.1
XM_005262893.1 4622 UTR 3 XP_005262950.1
XM_005262896.1 4622 UTR 3 XP_005262953.1
XM_005262897.2 4622 Intron XP_005262954.1
XM_005262898.2 4622 UTR 3 XP_005262955.1
XM_011531830.1 4622 UTR 3 XP_011530132.1
XM_011531831.1 4622 UTR 3 XP_011530133.1
XM_011531832.1 4622 UTR 3 XP_011530134.1
XM_017007989.1 4622 UTR 3 XP_016863478.1

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