Variant #0000654191 (NC_000002.11:g.127816618_127816629del, NM_139343.2:c.969_980del (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.127816618_127816629del
DNA change (hg38) g.127059042_127059053del
Published as BIN1(NM_004305.3):c.921_932del (p.(Pro308_Thr311del))
ISCN -
DB-ID BIN1_000051
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2020-03-23 16:13:27 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BIN1 NM_139343.2 ?/. - c.969_980del r.(?) p.(Pro324_Thr327del)


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