Variant #0000236467 (NC_000002.11:g.127827669G>C, NC_000002.11(NM_139343.2):c.316-3C>G (BIN1))

Chromosome 2
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.127827669G>C
DNA change (hg38) g.127070093G>C
Published as -
ISCN -
DB-ID BIN1_000036
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs113742431
Origin Germline
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 2010-12-28 11:40:11 +01:00 (CET)
Date last edited 2012-11-02 20:40:23 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BIN1 NM_139343.2 ?/. 4i c.316-3C>G r.(=) p.(=)


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