Variant #0000274759 (NC_000002.11:g.172309724G>A, NC_000002.11(NM_025000.3):c.627+1G>A (DCAF17))

Chromosome 2
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.172309724G>A
DNA change (hg38) g.171453214G>A
Published as DCAF17(NM_025000.3):c.627+1G>A
ISCN -
DB-ID DCAF17_000009
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) 1.0E-5 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 2020-06-09 19:25:06 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
METTL8 NM_024770.3 +/. - c.-18553C>T r.(?) p.(=)
DCAF17 NM_025000.3 +/. - c.627+1G>A r.spl? p.?


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