Variant #0000271074 (NC_000019.9:g.11618630G>A, NM_016581.4:c.832C>T (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.11618630G>A
DNA change (hg38) g.11507815G>A
Published as ECSIT(NM_016581.5):c.832C>T (p.R278C)
ISCN -
DB-ID ECSIT_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) 0.04687 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ECSIT NM_016581.4 -?/. - c.832C>T r.(?) p.(Arg278Cys)
ZNF653 NM_138783.3 -?/. - c.-2029C>T r.(?) p.(=)


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