Product Details

SNP ID
rs11542697
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.9:105694739 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCCCTTTTTTGACATCGCGCACTAT[C/G]TAGTGTCAGTGATGGCGGTGAAACG
Phenotype
MIM: 611236
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
TMEM38B PubMed Links

Gene Details

Gene
TMEM38B
Gene Name
transmembrane protein 38B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_018112.2 207 Missense Mutation CTA,GTA L27V NP_060582.1
XM_005252075.2 207 Intron XP_005252132.1
XM_005252076.2 207 Missense Mutation CTA,GTA L27V XP_005252133.1
XM_005252077.3 207 Missense Mutation CTA,GTA L27V XP_005252134.1
XM_011518829.1 207 Missense Mutation CTA,GTA L27V XP_011517131.1
XM_011518831.2 207 Missense Mutation CTA,GTA L27V XP_011517133.1
XM_011518832.2 207 Missense Mutation CTA,GTA L27V XP_011517134.1
XM_011518833.2 207 UTR 5 XP_011517135.1

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