Variant #0000726312 (NC_000017.10:g.34893558T>G, NM_004773.3:c.*42310T>G (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.34893558T>G
DNA change (hg38) -
Published as PIGW(NM_178517.4):c.608T>G (p.L203W)
ISCN -
DB-ID MYO19_000007
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) 1.0E-5 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ZNHIT3 NM_004773.3 ?/. - c.*42310T>G r.(=) p.(=)
MYO19 NM_025109.5 ?/. - c.-3266A>C r.(?) p.(=)
PIGW NM_178517.3 ?/. - c.608T>G r.(?) p.(Leu203Trp)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.