Variant #0000692317 (NC_000017.10:g.34894082G>C, NM_004773.3:c.*42834G>C (ZNHIT3))

Chromosome 17
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.34894082G>C
DNA change (hg38) -
Published as PIGW(NM_178517.4):c.1132G>C (p.V378L)
ISCN -
DB-ID MYO19_000012
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) 0.00071 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 2020-09-15 15:50:26 +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     
ZNHIT3 NM_004773.3 -?/. - c.*42834G>C r.(=) p.(=)
MYO19 NM_025109.5 -?/. - c.-3790C>G r.(?) p.(=)
PIGW NM_178517.3 -?/. - c.1132G>C r.(?) p.(Val378Leu)


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