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Variant : CV363272 (NM_001904.4(CTNNB1):c.97T>A (p.Ser33Thr)) Homo sapiens

Symbol: CV363272
Name: NM_001904.4(CTNNB1):c.97T>A (p.Ser33Thr)
Condition: Adenocarcinoma of lung [RCV000437702]|Adenocarcinoma of prostate [RCV000424580]|Adenocarcinoma of stomach [RCV000440157]|Carcinoma of esophagus [RCV000431206]|Colorectal Neoplasms [RCV000420531]|Hepatocellular carcinoma [RCV000425706]|Lung adenocarcinoma [RCV000437702]|Malignant melanoma of skin [RCV000427045]|Malignant neoplasm of body of uterus [RCV000432938]|Medulloblastoma [RCV000441880]|Neoplasm of the large intestine [RCV000420531]|Oesophageal carcinoma [RCV000431206]|Pancreatic adenocarcinoma [RCV000418116]|Transitional cell carcinoma of the bladder [RCV000435335]
Clinical Significance: likely pathogenic
Last Evaluated: 05/31/2016
Review Status: no assertion criteria provided
Related Genes: CTNNB1  
Variant Type: single nucleotide variant (SO:0001583)
Source: CLINVAR
Molecular Consequence: missense variant
Evidence: literature only
HGVS Name(s): NP_001091679.1:p.Ser33Thr
NP_001091680.1:p.Ser33Thr
NG_013302.2:g.30159T>A
NC_000003.12:g.41224609T>A
NC_000003.11:g.41266100T>A
NP_001895.1:p.Ser33Thr
NM_001330729.2:c.76T>A
NM_001098209.2:c.97T>A
NM_001098210.2:c.97T>A
NM_001904.4:c.97T>A
NP_001317658.1:p.Ser26Thr
Position
Human AssemblyChrPosition (strand)Source
GRCh38341,224,609 - 41,224,609CLINVAR
GRCh37341,266,100 - 41,266,100CLINVAR
Cytogenetic Map33p22.1CLINVAR
Trait Synonyms: Adenocarcinoma of lung; Adenocarcinoma of lung, somatic; Colorectal Neoplasms; Esophageal carcinoma; Increased hepatocellular carcinoma risk; Increased incidence of hepatocellular carcinoma; Large intestine tumor; Liver cancer; LIVER CELL CARCINOMA; Medulloblastoma, somatic; MELANOMA, MALIGNANT, SOMATIC; Oesophageal carcinoma; Primary carcinoma of liver; Transitional cell bladder carcinoma
Prevalence: 1-9 / 1 000 000



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 12834772
Created: 2017-04-11
Species: Homo sapiens
Last Modified: 2019-12-03
Status: ACTIVE



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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.