Variant #0000302679 (NC_000017.10:g.34859015G>A, NM_004773.3:c.*7767G>A (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.34859015G>A
DNA change (hg38) g.36503175G>A
Published as MYO19(NM_001163735.1):c.2002C>T (p.L668F)
ISCN -
DB-ID MYO19_000003
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) 5.0E-5 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-13 12:20:05 +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.*7767G>A r.(=) p.(=)
MYO19 NM_025109.5 ?/. - c.1402C>T r.(?) p.(Arg468Ter)


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