Product Details

SNP ID
rs144521316
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.10:14897012 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGCAAAGCAATAACTCCAAAAGACA[A/G]TAACAAAACTTTGAAACCTGCCATT
Phenotype
MIM: 605988 MIM: 606503
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
DCLRE1C PubMed Links

Gene Details

Gene
DCLRE1C
Gene Name
DNA cross-link repair 1C
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001033855.2 651 Intron NP_001029027.1
NM_001033857.2 651 Intron NP_001029029.1
NM_001033858.2 651 Intron NP_001029030.1
NM_001289076.1 651 Intron NP_001276005.1
NM_001289077.1 651 Intron NP_001276006.1
NM_001289078.1 651 Intron NP_001276007.1
NM_001289079.1 651 Intron NP_001276008.1
NM_022487.3 651 Intron NP_071932.2
XM_006717491.3 651 Intron XP_006717554.1
XM_011519616.1 651 Intron XP_011517918.1
XM_011519617.1 651 Intron XP_011517919.1
XM_011519619.1 651 Intron XP_011517921.1
XM_011519620.2 651 Intron XP_011517922.1
XM_011519621.1 651 Intron XP_011517923.1
XM_017016556.1 651 Intron XP_016872045.1
XM_017016557.1 651 Intron XP_016872046.1
XM_017016558.1 651 Intron XP_016872047.1
XM_017016559.1 651 Intron XP_016872048.1
XM_017016560.1 651 Intron XP_016872049.1
Gene
SUV39H2
Gene Name
suppressor of variegation 3-9 homolog 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001193424.1 651 Missense Mutation AAT,AGT N115S NP_001180353.1
NM_001193425.1 651 Missense Mutation AAT,AGT N55S NP_001180354.1
NM_001193426.1 651 Intron NP_001180355.1
NM_001193427.1 651 Intron NP_001180356.1
NM_024670.3 651 Missense Mutation AAT,AGT N55S NP_078946.1
XM_006717503.3 651 Missense Mutation AAT,AGT N55S XP_006717566.1
XM_011519662.2 651 Missense Mutation AAT,AGT N55S XP_011517964.1
XM_017016637.1 651 Missense Mutation AAT,AGT N55S XP_016872126.1

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