Variant #0000262718 (NC_000014.8:g.104029307C>G, NM_032374.3:c.8C>G (APOPT1))

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.104029307C>G
DNA change (hg38) g.103562970C>G
Published as APOPT1(NM_032374.4):c.8C>G (p.P3R)
ISCN -
DB-ID APOPT1_000002
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) 0.00067 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BAG5 NM_001015048.2 ?/. - c.-383G>C r.(?) p.(=)
APOPT1 NM_032374.3 ?/. - c.8C>G r.(?) p.(Pro3Arg)


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