Product Details

SNP ID
rs9171
Assay Type
Validated
NCBI dbSNP Submissions
NA
Location
Chr.20:3753739 on Build GRCh38
Set Membership
Validated
Context Sequence [VIC/FAM]
GTCCTCTCCCAGACCCTGGTGGGAG[C/T]CCCTGTGGCTTGGGGTGGGGAGTGG
Phenotype
MIM: 610702
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
C20orf27 PubMed Links

Gene Details

Gene
C20orf27
Gene Name
chromosome 20 open reading frame 27
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001039140.2 1527 UTR 3 NP_001034229.1
NM_001258429.1 1527 UTR 3 NP_001245358.1
NM_001258430.1 1527 UTR 3 NP_001245359.1
XM_011529266.2 1527 UTR 3 XP_011527568.1
Gene
HSPA12B
Gene Name
heat shock protein family A (Hsp70) member 12B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001197327.1 1527 Intron NP_001184256.1
NM_001318322.1 1527 Intron NP_001305251.1
NM_052970.4 1527 Intron NP_443202.3
XM_011529151.2 1527 Intron XP_011527453.1
XM_017027632.1 1527 Intron XP_016883121.1
XM_017027633.1 1527 Intron XP_016883122.1
XM_017027634.1 1527 Intron XP_016883123.1
XM_017027635.1 1527 Intron XP_016883124.1

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