Product Details

SNP ID
rs199692915
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.19:45468691 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTTCGGTGGACTCCTTCGGCAGTCC[A/C]CCCACCGCCGCCGCCTCCCAGGTAA
Phenotype
MIM: 126380 MIM: 164772
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
ERCC1 PubMed Links

Gene Details

Gene
ERCC1
Gene Name
ERCC excision repair 1, endonuclease non-catalytic subunit
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001166049.1 697 Intron NP_001159521.1
NM_001983.3 697 Intron NP_001974.1
NM_202001.2 697 Intron NP_973730.1
XM_005258634.1 697 Intron XP_005258691.1
XM_005258635.2 697 Intron XP_005258692.1
XM_005258636.4 697 Intron XP_005258693.1
XM_005258637.1 697 Intron XP_005258694.1
XM_011526610.2 697 Intron XP_011524912.1
XM_017026459.1 697 Intron XP_016881948.1
XM_017026460.1 697 Intron XP_016881949.1
XM_017026461.1 697 Intron XP_016881950.1
XM_017026462.1 697 Intron XP_016881951.1
XM_017026463.1 697 Intron XP_016881952.1
XM_017026464.1 697 Intron XP_016881953.1
XM_017026465.1 697 Intron XP_016881954.1
XM_017026466.1 697 Intron XP_016881955.1
Gene
FOSB
Gene Name
FosB proto-oncogene, AP-1 transcription factor subunit
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001114171.1 697 Silent Mutation CCA,CCC P35P NP_001107643.1
NM_006732.2 697 Silent Mutation CCA,CCC P35P NP_006723.2
XM_005258691.1 697 Silent Mutation CCA,CCC P35P XP_005258748.1

View Full Product Details