Variant #0000510256 (NC_000002.11:g.172330477T>C, NM_025000.3:c.1083T>C (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.172330477T>C
DNA change (hg38) g.171473967T>C
Published as DCAF17(NM_025000.3):c.1083T>C (p.N361=)
ISCN -
DB-ID DCAF17_000027
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) 7.0E-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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-08-06 14:59:34 +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.-39306A>G r.(?) p.(=)
DCAF17 NM_025000.3 -?/. - c.1083T>C r.(?) p.(Asn361=)


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