Variant #0000849078 (NC_000002.11:g.172330424T>C, NM_025000.3:c.1030T>C (DCAF17))

Chromosome 2
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.172330424T>C
DNA change (hg38) -
Published as DCAF17(NM_025000.3):c.1030T>C (p.W344R), DCAF17(NM_025000.4):c.1030T>C (p.W344R)
ISCN -
DB-ID DCAF17_000025 See all 2 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) 0.00059 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 2022-05-09 15:40:45 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
METTL8 NM_024770.3 ?/. - c.-39253A>G r.(?) p.(=)
DCAF17 NM_025000.3 ?/. - c.1030T>C r.(?) p.(Trp344Arg)


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