Variant #0000268649 (NC_000002.11:g.172291616C>T, NM_025000.3:c.150C>T (DCAF17))

Chromosome 2
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.172291616C>T
DNA change (hg38) g.171435106C>T
Published as DCAF17(NM_025000.3):c.150C>T (p.V50=), DCAF17(NM_025000.4):c.150C>T (p.V50=)
ISCN -
DB-ID DCAF17_000002 See all 3 reported entries
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) 0.27519 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +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.-445G>A r.(?) p.(=)
DCAF17 NM_025000.3 -?/. - c.150C>T r.(?) p.(Val50=)


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