Variant #0000236464 (NC_000002.11:g.127834262C>A, NM_139343.2:c.105G>T (BIN1))

Chromosome 2
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.127834262C>A
DNA change (hg38) g.127076686C>A
Published as -
ISCN -
DB-ID BIN1_000001 See all 4 reported entries
Variant remarks expression cloning COS-1 cells abolished membrane tubulation
Reference PubMed: Nicot 2007, OMIM:var0001
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2010-03-12 10:36:48 +01:00 (CET)
Date last edited 2020-07-14 21:50:58 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BIN1 NM_139343.2 +/. 2 c.105G>T r.(?) p.Lys35Asn


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