Variant #0000532676 (NC_000007.13:g.76069618del, NM_001110354.1:c.883del (ZP3))

Chromosome 7
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.76069618del
DNA change (hg38) g.76440301del
Published as ZP3(NM_007155.5):c.730delG (p.E244Nfs*46)
ISCN -
DB-ID SRCRB4D_000002
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) 0.00047 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-23 09:57:03 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ZP3 NM_001110354.1 +/. - c.883del r.(?) p.(Glu295AsnfsTer46)
SRCRB4D NM_080744.1 +/. - c.-30954del r.(?) p.(=)


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