Bibliome.ai browser hg19
Search
About
Stats
FAQ
LDLR c.902A>T ;(p.D301V)
Variant ID: 19-11218152-A-T
NM_000527.4(
LDLR
):c.902A>T;(p.D301V)
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:
Effects of Different Types of Pathogenic Variants on Phenotypes of Familial Hypercholesterolemia.
Frontiers In Genetics
Tada, Hayato H; Kojima, Nobuko N; Yamagami, Kan K; Nomura, Akihiro A; Nohara, Atsushi A; Usui, Soichiro S; Sakata, Kenji K; Fujino, Noboru N; Takamura, Masayuki M; Kawashiri, Masa-Aki MA
Publication Date: 2022
Variant appearance in text: LDLR: 902A>T; Asp301Val
PubMed Link:
35480308
Variant Present in the following documents:
Presentation1.pdf
View BVdb publication page