Variant #0000267275 (NC_000002.11:g.172305177C>T, NC_000002.11(NM_025000.3):c.322-14C>T (DCAF17))

Chromosome 2
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.172305177C>T
DNA change (hg38) g.171448667C>T
Published as DCAF17(NM_025000.3):c.322-14C>T, DCAF17(NM_025000.4):c.322-14C>T
ISCN -
DB-ID DCAF17_000007 See all 4 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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
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.-14006G>A r.(?) p.(=)
DCAF17 NM_025000.3 -/. - c.322-14C>T r.(=) p.(=)


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