Variant #0000561060 (NC_000017.10:g.3374975_3374976del, NM_000049.2:c.-4479_-4478del (ASPA))

Chromosome 17
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.3374975_3374976del
DNA change (hg38) g.3471681_3471682del
Published as SPATA22(NM_001170698.1):c.-74+2_-74+3del (p.(=))
ISCN -
DB-ID SPATA22_000001
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 2025-02-07 18:57:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ASPA NM_000049.2 -?/. - c.-4479_-4478del r.(?) p.(=)
TRPV3 NM_145068.3 -?/. - c.*42237_*42238del r.(=) p.(=)


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