Variant #0000687825 (NC_000001.10:g.118495168A>G, NM_206996.2:c.*1505T>C (SPAG17))

Chromosome 1
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.118495168A>G
DNA change (hg38) -
Published as WDR3(NM_006784.3):c.2034A>G (p.I678M)
ISCN -
DB-ID SPAG17_000003
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) 1.0E-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 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
WDR3 NM_006784.2 ?/. - c.2034A>G r.(?) p.(Ile678Met)
SPAG17 NM_206996.2 ?/. - c.*1505T>C r.(=) p.(=)


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