UniProtKB/Swiss-Prot P01116 : Variant p.Gly12Val
GTPase KRas
Gene: KRAS
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Variant information
Variant position:
12
The position of the amino-acid change on the UniProtKB canonical protein sequence.
Type of variant:
LP/P [Disclaimer : Variants classification is intended for research purposes only, not for clinical and diagnostic use . The label disease variant is assigned according to literature reports on probable disease-association that can be based on theoretical reasons. This label must not be considered as a definitive proof for the pathogenic role of a variant. ]
The variants are classified into three categories: LP/P, LB/B and US.LP/P: likely pathogenic or pathogenic. LB/B: likely benign or benign. US: uncertain significance
Residue change:
From Glycine (G) to Valine (V) at position 12 (G12V, p.Gly12Val).
Indicates the amino acid change of the variant. The one-letter and three-letter codes for amino acids used in UniProtKB/Swiss-Prot are those adopted by the commission on Biochemical Nomenclature of the IUPAC-IUB.
Physico-chemical properties:
Change from glycine (G) to medium size and hydrophobic (V)
The physico-chemical property of the reference and variant residues and the change implicated.
BLOSUM score:
-3
The score within a Blosum matrix for the corresponding wild-type to variant amino acid change. The log-odds score measures the logarithm for the ratio of the likelihood of two amino acids appearing by chance. The Blosum62 substitution matrix is used. This substitution matrix contains scores for all possible exchanges of one amino acid with another: Lowest score: -4 (low probability of substitution).Highest score: 11 (high probability of substitution). More information can be found on the following page
Variant description:
In GASC; also found in lung carcinoma, pancreatic carcinoma and colon cancer; also found in metastatic colorectal cancer; somatic mutation; it is constitutively activated and stimulates transcription activation of tumor suppressor genes in non-transformed fibroblasts.
Any additional useful information about the variant.
Other resources:
Links to websites of interest for the variant.
Sequence information
Variant position:
12
The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length:
189
The length of the canonical sequence.
Location on the sequence:
MTEYKLVVVGA
G GVGKSALTIQLIQNHFVDEY
The residue change on the sequence. Unless the variant is located at the beginning or at the end of the protein sequence, both residues upstream (20) and downstream (20) of the variant will be shown.
Residue conservation:
The multiple alignment of the region surrounding the variant against various orthologous sequences.
Human MTEYKLVVVGAG GVGKSALTIQLIQNHFVDEY
Mouse MTEYKLVVVGAG GVGKSALTIQLIQNHFVDEY
Rat MTEYKLVVVGAG GVGKSALTIQLIQNHFVDEY
Xenopus laevis MTEYKLVVVGAV GVGKSALTIQLIQNHFVDEY
Sequence annotation in neighborhood:
The regions or sites of interest surrounding the variant. In general the features listed are posttranslational modifications, binding sites, enzyme active sites, local secondary structure or other characteristics reported in the cited references. The "Sequence annotation in neighborhood" lines have a fixed format:Type: the type of sequence feature. Positions: endpoints of the sequence feature. Description: contains additional information about the feature.
Type Positions Description
Chain
1 – 186
GTPase KRas
Initiator methionine
1 – 1
Removed; alternate
Chain
2 – 186
GTPase KRas, N-terminally processed
Binding site
10 – 18
Modified residue
1 – 1
N-acetylmethionine; in GTPase KRas; alternate
Modified residue
2 – 2
N-acetylthreonine; in GTPase KRas, N-terminally processed
Beta strand
12 – 14
Literature citations
Human colon carcinoma Ki-ras2 oncogene and its corresponding proto-oncogene.
McCoy M.S.; Bargmann C.I.; Weinberg R.A.;
Mol. Cell. Biol. 4:1577-1582(1984)
Cited for: NUCLEOTIDE SEQUENCE [GENOMIC DNA] (ISOFORMS 2A AND 2B); VARIANT COLON CANCER VAL-12;
Activated c-Ha-ras oncogene with a guanine to thymine transversion at the twelfth codon in a human stomach cancer cell line.
Deng G.; Lu Y.; Chen S.; Miao J.; Lu G.; Li H.; Cai H.; Xu X.; Zheng E.; Liu P.;
Cancer Res. 47:3195-3198(1987)
Cited for: NUCLEOTIDE SEQUENCE [GENOMIC DNA] OF 1-37; VARIANT GASC VAL-12;
Regulation of RAS oncogenicity by acetylation.
Yang M.H.; Nickerson S.; Kim E.T.; Liot C.; Laurent G.; Spang R.; Philips M.R.; Shan Y.; Shaw D.E.; Bar-Sagi D.; Haigis M.C.; Haigis K.M.;
Proc. Natl. Acad. Sci. U.S.A. 109:10843-10848(2012)
Cited for: ACETYLATION AT LYS-104; VARIANT VAL-12; FUNCTION; ACTIVITY REGULATION;
A KRAS-directed transcriptional silencing pathway that mediates the CpG island methylator phenotype.
Serra R.W.; Fang M.; Park S.M.; Hutchinson L.; Green M.R.;
Elife 3:E02313-E02313(2014)
Cited for: FUNCTION; CHARACTERIZATION OF VARIANT COLON CANCER VAL-12;
Detection of point mutations in the Kirsten-ras oncogene provides evidence for the multicentricity of pancreatic carcinoma.
Motojima K.; Urano T.; Nagata Y.; Shiku H.; Tsurifune T.; Kanematsu T.;
Ann. Surg. 217:138-143(1993)
Cited for: VARIANTS PANCREATIC CARCINOMA ASP-12 AND VAL-12;
BRAF and KRAS mutations in stomach cancer.
Lee S.H.; Lee J.W.; Soung Y.H.; Kim H.S.; Park W.S.; Kim S.Y.; Lee J.H.; Park J.Y.; Cho Y.G.; Kim C.J.; Nam S.W.; Kim S.H.; Lee J.Y.; Yoo N.J.;
Oncogene 22:6942-6945(2003)
Cited for: VARIANTS GASC ASN-5; VAL-12; ASP-13 AND THR-59;
Distinct epidermal growth factor receptor and KRAS mutation patterns in non-small cell lung cancer patients with different tobacco exposure and clinicopathologic features.
Tam I.Y.S.; Chung L.P.; Suen W.S.; Wang E.; Wong M.C.M.; Ho K.K.; Lam W.K.; Chiu S.W.; Girard L.; Minna J.D.; Gazdar A.F.; Wong M.P.;
Clin. Cancer Res. 12:1647-1653(2006)
Cited for: VARIANTS LUNG CARCINOMA CYS-12; ASP-12; SER-12; VAL-12 AND HIS-61;
The consensus coding sequences of human breast and colorectal cancers.
Sjoeblom T.; Jones S.; Wood L.D.; Parsons D.W.; Lin J.; Barber T.D.; Mandelker D.; Leary R.J.; Ptak J.; Silliman N.; Szabo S.; Buckhaults P.; Farrell C.; Meeh P.; Markowitz S.D.; Willis J.; Dawson D.; Willson J.K.V.; Gazdar A.F.; Hartigan J.; Wu L.; Liu C.; Parmigiani G.; Park B.H.; Bachman K.E.; Papadopoulos N.; Vogelstein B.; Kinzler K.W.; Velculescu V.E.;
Science 314:268-274(2006)
Cited for: VARIANTS [LARGE SCALE ANALYSIS] ALA-12; ASP-12; SER-12; VAL-12; ASP-13; ARG-61; ASN-117 AND THR-146;
KRAS A146 mutations are associated with distinct clinical behavior in patients with colorectal liver metastases.
van 't Erve I.; Wesdorp N.J.; Medina J.E.; Ferreira L.; Leal A.; Huiskens J.; Bolhuis K.; van Waesberghe J.T.M.; Swijnenburg R.J.; van den Broek D.; Velculescu V.E.; Kazemier G.; Punt C.J.A.; Meijer G.A.; Fijneman R.J.A.;
JCO Precis. Oncol. 5:0-0(2021)
Cited for: VARIANTS ALA-12; ASP-12; CYS-12; VAL-12; ASN-117 AND THR-146;
Disclaimer:
Any medical or genetic information present in this entry is provided for research, educational and informational purposes only. They are not in any way intended to be used as a substitute for professional medical advice, diagnostic, treatment or care.