Variant #0000676114 (NC_000002.11:g.172314497C>T, NM_025000.3:c.644C>T (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.172314497C>T
DNA change (hg38) -
Published as DCAF17(NM_025000.3):c.644C>T (p.T215I)
ISCN -
DB-ID DCAF17_000030
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2020-09-15 15:50:26 +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.-23326G>A r.(?) p.(=)
DCAF17 NM_025000.3 ?/. - c.644C>T r.(?) p.(Thr215Ile)


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