Product Details

SNP ID
rs111355817
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.20:3754082 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTCAGTCAAAGCCGTGCCAGTCGCT[A/G]TGCTCTGAGTCGTATTCCAGCTCGG
Phenotype
MIM: 610702
Polymorphism
A/G, 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 1184 Silent Mutation CAC,CAT H192H NP_001034229.1
NM_001258429.1 1184 Silent Mutation CAC,CAT H167H NP_001245358.1
NM_001258430.1 1184 Silent Mutation CAC,CAT H167H NP_001245359.1
XM_011529266.2 1184 Silent Mutation CAC,CAT H151H 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 1184 Intron NP_001184256.1
NM_001318322.1 1184 Intron NP_001305251.1
NM_052970.4 1184 Intron NP_443202.3
XM_011529151.2 1184 Intron XP_011527453.1
XM_017027632.1 1184 Intron XP_016883121.1
XM_017027633.1 1184 Intron XP_016883122.1
XM_017027634.1 1184 Intron XP_016883123.1
XM_017027635.1 1184 Intron XP_016883124.1

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