Variant #0000326210 (NC_000019.9:g.11624065G>C, NM_016581.4:c.544C>G (ECSIT))

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.11624065G>C
DNA change (hg38) g.11513250G>C
Published as ECSIT(NM_001142464.2):c.544C>G (p.(Leu182Val))
ISCN -
DB-ID ECSIT_000004
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) 1.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ECSIT NM_016581.4 ?/. - c.544C>G r.(?) p.(Leu182Val)
ZNF653 NM_138783.3 ?/. - c.-7464C>G r.(?) p.(=)


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