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TG c.4956A>G ;(p.S1652=)
Variant ID: 8-133948024-A-G
NM_003235.4(
TG
):c.4956A>G;(p.S1652=)
This variant was identified in 1 publication
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
BRCA1/BRCA2 mutation spectrum analysis in South Asia: a systematic review.
The Journal Of International Medical Research
Kharel, Sanjeev S; Shrestha, Suraj S; Yadav, Siddhartha S; Shakya, Prafulla P; Baidya, Sujita S; Hirachan, Suzita S
Publication Date: 2022-01
Variant appearance in text: TG: 4956A>G
PubMed Link:
35000471
Variant Present in the following documents:
sj-pdf-3-imr-10.1177_03000605211070757.pdf
View BVdb publication page
BRCA1/BRCA2 mutation spectrum analysis in South Asia: a systematic review.
The Journal Of International Medical Research
Kharel, Sanjeev S; Shrestha, Suraj S; Yadav, Siddhartha S; Shakya, Prafulla P; Baidya, Sujita S; Hirachan, Suzita S
Publication Date: 2022-01
Variant appearance in text: TG: 4956A>G
PubMed Link:
35000471
Variant Present in the following documents:
sj-pdf-3-imr-10.1177_03000605211070757.pdf
View BVdb publication page