Variant #0000561085 (NC_000017.10:g.34893567_34893570del, NM_004773.3:c.*42319_*42322del (ZNHIT3))

Chromosome 17
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.34893567_34893570del
DNA change (hg38) g.36537718_36537721del
Published as PIGW(NM_178517.4):c.617_620delTTTG (p.V206Gfs*3)
ISCN -
DB-ID MYO19_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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-13 12:20:47 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ZNHIT3 NM_004773.3 ?/. - c.*42319_*42322del r.(=) p.(=)
MYO19 NM_025109.5 ?/. - c.-3276_-3273del r.(?) p.(=)
PIGW NM_178517.3 ?/. - c.617_620del r.(?) p.(Val206GlyfsTer3)


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