Variant #0000521518 (NC_000004.11:g.123855735_123855737del, NM_145207.2:c.989_991del (SPATA5))

Chromosome 4
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.123855735_123855737del
DNA change (hg38) g.122934580_122934582del
Published as SPATA5(NM_145207.2):c.989_991delCAA (p.T330del), SPATA5(NM_145207.3):c.989_991del (p.(Thr330del)), SPATA5(NM_145207.3):c.989_991delCAA (p.T330del)
ISCN -
DB-ID SPATA5_000015 See all 11 reported entries
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
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     
SPATA5 NM_145207.2 +/. - c.989_991del r.(?) p.(Thr330del)


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