Variant #0000930834 (NC_000017.10:g.57322928A>T, NC_000017.10(NM_182569.3):c.321+18A>T (GDPD1))

Chromosome 17
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.57322928A>T
DNA change (hg38) -
Published as GDPD1(NM_182569.4):c.321+18A>T
ISCN -
DB-ID GDPD1_000000
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) 0.00087 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2023-07-07 10:10:56 +02:00 (CEST)
Date last edited 2023-08-17 14:00:11 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GDPD1 NM_182569.3 -?/. - c.321+18A>T r.(=) p.(=)


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