Variant #0000614722 (NC_000014.8:g.104028259G>C, NM_032374.3:c.-1041G>C (APOPT1))

Chromosome 14
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.104028259G>C
DNA change (hg38) g.103561922G>C
Published as BAG5(NM_001015049.2):c.86C>G (p.P29R)
ISCN -
DB-ID APOPT1_000010
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 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 2019-12-04 15:24:38 +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.-29+694C>G r.(=) p.(=)
APOPT1 NM_032374.3 -?/. - c.-1041G>C r.(?) p.(=)


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