Variant #0000949084 (NC_000008.10:g.55372276_55372287del, NM_022454.3:c.966_977del (SOX17))

Chromosome 8
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.55372276_55372287del
DNA change (hg38) -
Published as SOX17(NM_022454.4):c.966_977delGCACCAGCACCA (p.Q322_H325del)
ISCN -
DB-ID SOX17_000016
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 2023-11-27 17:35:39 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SOX17 NM_022454.3 ?/. - c.966_977del r.(?) p.(Gln322_His325del)


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