Geno
|
Mag
|
Summary
|
(A;C)
|
3
|
Drug response to cetuximab and panitumumab
|
(C;C)
|
0
|
common in clinvar
|
(G;G)
|
0
|
common in complete genomics
|
aka c.38G>T (p.Gly13Val)
annotated in ClinVar as a somatic mutation, and also for its PGx association (drug response to cetuximab and panitumumab)
23andMe name for the c.38G>A variant: i5002724
ClinVar
|
Risk
|
rs112445441(A;A) Rs112445441(G;G) rs112445441(T;T) |
Alt
|
rs112445441(A;A) Rs112445441(G;G) rs112445441(T;T) |
Reference
|
Rs112445441(C;C) |
Significance |
Drug-response |
Disease |
Non-small cell lung cancer cetuximab response - Dosage panitumumab response - Dosage Neoplasm of the thyroid gland Colorectal Neoplasms Breast adenocarcinoma Juvenile myelomonocytic leukemia RAS-associated autoimmune leukoproliferative disorder Acute myeloid leukemia Ovarian Neoplasms |
Variation | info |
---|
Gene |
KRAS |
CLNDBN |
Non-small cell lung cancer cetuximab response - Dosage panitumumab response - Dosage Neoplasm of the thyroid gland Colorectal Neoplasms Breast adenocarcinoma Juvenile myelomonocytic leukemia RAS-associated autoimmune leukoproliferative disorder Acute myeloid leukemia Ovarian Neoplasms |
Reversed |
0 |
HGVS |
NC_000012.11:g.25398281C>A; NC_000012.11:g.25398281C>G; NC_000012.11:g.25398281C>T |
CLNSRC |
OMIM Allelic Variant UniProtKB (protein) |
CLNACC |
RCV000038270.2, RCV000417135.1, RCV000417162.1, RCV000422238.1, RCV000439931.1, RCV000431622.1, RCV000444986.1, RCV000013409.6, RCV000038269.3, RCV000144967.4, RCV000144968.4, RCV000421576.1, RCV000427102.1, RCV000431806.1, RCV000444192.1, |