Variant #0000538224 (NC_000009.11:g.40705403G>C, NM_001083124.1:c.3060G>C (SPATA31A3))

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.40705403G>C
DNA change (hg38) g.66987438C>G
Published as SPATA31A3(NM_001083124.1):c.3060G>C (p.(Lys1020Asn))
ISCN -
DB-ID SPATA31A3_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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SPATA31A3 NM_001083124.1 ?/. - c.3060G>C r.(?) p.(Lys1020Asn)


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