Variant #0000657518 (NC_000014.8:g.96775935T>C, NC_000014.8(NM_018036.5):c.4162-4A>G (ATG2B))

Chromosome 14
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.96775935T>C
DNA change (hg38) g.96309598T>C
Published as ATG2B(NM_018036.5):c.4162-4A>G (p.?)
ISCN -
DB-ID ATG2B_000006
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 2020-07-05 16:46:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ATG2B NM_018036.5 ?/. - c.4162-4A>G r.spl? p.?


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