Variant #0000973208 (NC_000001.10:g.118584599T>G, NM_206996.2:c.2881A>C (SPAG17))

Chromosome 1
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.118584599T>G
DNA change (hg38) -
Published as SPAG17(NM_206996.4):c.2881A>C (p.(Lys961Gln))
ISCN -
DB-ID SPAG17_000005
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:20:39 +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.*82529T>G r.(=) p.(=)
SPAG17 NM_206996.2 -?/. - c.2881A>C r.(?) p.(Lys961Gln)


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