Product Details

SNP ID
rs28383110
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.5:83077430 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCCTCTCCAGCCGTCCGGTTGGGCT[C/T]GTCACGGCACCGCCTACCAAGACGG
Phenotype
MIM: 194363
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
TMEM167A PubMed Links

Gene Details

Gene
TMEM167A
Gene Name
transmembrane protein 167A
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_174909.4 22 Intron NP_777569.1
Gene
XRCC4
Gene Name
X-ray repair cross complementing 4
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001318012.1 22 UTR 5 NP_001304941.1
NM_001318013.1 22 UTR 5 NP_001304942.1
NM_003401.4 22 UTR 5 NP_003392.1
NM_022406.3 22 UTR 5 NP_071801.1
NM_022550.3 22 UTR 5 NP_072044.1
XM_011543626.1 22 Intron XP_011541928.1
XM_017009827.1 22 UTR 5 XP_016865316.1
XM_017009828.1 22 UTR 5 XP_016865317.1
XM_017009829.1 22 UTR 5 XP_016865318.1

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