Variant #0000515066 (NC_000002.11:g.233344925G>A, NM_004826.2:c.2266C>T (ECEL1))

Chromosome 2
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.233344925G>A
DNA change (hg38) g.232480215G>A
Published as ECEL1(NM_004826.2):c.2266C>T (p.(Arg756Trp)), ECEL1(NM_004826.3):c.2266C>T (p.R756W)
ISCN -
DB-ID ECEL1_000017 See all 2 reported entries
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) 0.00025 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ECEL1 NM_004826.2 ?/. - c.2266C>T r.(?) p.(Arg756Trp)


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