Variant #0000863391 (NC_000013.10:g.46541921_46541932del, NM_015070.3:c.4038_4049del (ZC3H13))

Chromosome 13
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.46541921_46541932del
DNA change (hg38) -
Published as ZC3H13(NM_001330566.1):c.4038_4049delGAGAGAACGAGA (p.E1346_R1349del)
ISCN -
DB-ID ZC3H13_000008
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ZC3H13 NM_015070.3 ?/. - c.4038_4049del r.(?) p.(Glu1346_Arg1349del)


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