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RET c.74-7333G>T
Variant ID: 10-43588574-G-T
NM_020975.4(
RET
):c.74-7333G>T
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:
A multi-enhancer RET regulatory code is disrupted in Hirschsprung disease.
Genome Research
Chatterjee, Sumantra S; Karasaki, Kameko M KM; Fries, Lauren E LE; Kapoor, Ashish A; Chakravarti, Aravinda A
Publication Date: 2021-11-15
Variant appearance in text: rs7393733
PubMed Link:
34782358
Variant Present in the following documents:
Main text
2199.pdf
View BVdb publication page