RET c.3049G>A ;(p.D1017N)

Variant ID: 10-43622032-G-A

NM_020975.4(RET):c.3049G>A;(p.D1017N)

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:

The RET proto-oncogene induces apoptosis: a novel mechanism for Hirschsprung disease.

The Embo Journal
Bordeaux, M C MC; Forcet, C C; Granger, L L; Corset, V V; Bidaud, C C; Billaud, M M; Bredesen, D E DE; Edery, P P; Mehlen, P P
Publication Date: 2000-08-01

Variant appearance in text: RET: D1017N
PubMed Link: 10921886
Variant Present in the following documents:
  • Main text
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