Variant #0000692676 (NC_000019.9:g.11596563C>T, NM_001420.3:c.-5140G>A (ELAVL3))

Chromosome 19
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.11596563C>T
DNA change (hg38) -
Published as ZNF653(NM_138783.4):c.1478G>A (p.R493Q)
ISCN -
DB-ID ECSIT_000010
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) 4.0E-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 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     
ELAVL3 NM_001420.3 ?/. - c.-5140G>A r.(?) p.(=)
ECSIT NM_016581.4 ?/. - c.*20436G>A r.(=) p.(=)
ZNF653 NM_138783.3 ?/. - c.1478G>A r.(?) p.(Arg493Gln)


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