Variant #0000692677 (NC_000019.9:g.11616546C>T, NM_016581.4:c.*453G>A (ECSIT))

Chromosome 19
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.11616546C>T
DNA change (hg38) -
Published as ZNF653(NM_138783.4):c.56G>A (p.G19D)
ISCN -
DB-ID ECSIT_000011
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 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     
ECSIT NM_016581.4 -?/. - c.*453G>A r.(=) p.(=)
ZNF653 NM_138783.3 -?/. - c.56G>A r.(?) p.(Gly19Asp)


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