Variant #0000331634 (NC_000007.13:g.76069666_76069668del, NC_000007.13(NM_001110354.1):c.923+8_923+10del (ZP3))

Chromosome 7
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.76069666_76069668del
DNA change (hg38) g.76440349_76440351del
Published as ZP3(NM_001110354.1):c.923+3_923+5del (p.?)
ISCN -
DB-ID ZP3_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) 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ZP3 NM_001110354.1 ?/. - c.923+8_923+10del r.(=) p.(=)
SRCRB4D NM_080744.1 ?/. - c.-30999_-30997del r.(?) p.(=)


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