Bibliome.ai browser hg19
Search
About
Stats
FAQ
MVK c.227-660T>C
Variant ID: 12-110016947-T-C
NM_000431.2(
MVK
):c.227-660T>C
This variant was identified in 2 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Analysis of clinical characteristics and genetic testing in patients with acute fatty liver of pregnancy: a retrospective study.
Bmc Pregnancy And Childbirth
Shi, Yixian Y; Wu, Haicong H; Zhou, Xiaoling X; Xu, Qingling Q; Zheng, Liqing L; Li, Dongliang D; Yao, Lvfeng L
Publication Date: 2021-09-08
Variant appearance in text: rs7296044
PubMed Link:
34496798
Variant Present in the following documents:
12884_2021_4095_MOESM3_ESM.xlsx, sheet 1
View BVdb publication page
Novel germline TRAF3IP3 mutation in a dyad with familial acute B lymphoblastic leukemia.
Cancer Reports (Hoboken, N.J.)
Pommert, Lauren L; Burns, Robert R; Furumo, Quinlan Q; Pulakanti, Kirthi K; Brandt, Jon J; Burke, Michael J MJ; Rao, Sridhar S
Publication Date: 2021-06
Variant appearance in text: rs7296044
PubMed Link:
33503336
Variant Present in the following documents:
CNR2-4-e1335-s003.xlsx, sheet 2
View BVdb publication page