Variant #0001053282 (NC_000009.11:g.90534192_90534202del, NM_001145124.1:c.212_222del (SPATA31C1))

Chromosome 9
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.90534192_90534202del
DNA change (hg38) -
Published as SPATA31C1(NM_001145124.1):c.212_222del (p.(His71ProfsTer23))
ISCN -
DB-ID SPATA31C1_000006
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 2025-11-01 13:22:20 +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     
SPATA31C1 NM_001145124.1 ?/. - c.212_222del r.(?) p.(His71Profs*23)


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