Variant #0000265819 (NC_000002.11:g.233350938G>T, NM_004826.2:c.426C>A (ECEL1))

Chromosome 2
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.233350938G>T
DNA change (hg38) g.232486228G>T
Published as ECEL1(NM_001290787.1):c.426C>A (p.(Asp142Glu)), ECEL1(NM_004826.4):c.426C>A (p.D142E)
ISCN -
DB-ID ECEL1_000011 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) 0.00801 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-11-27 17:27:23 +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.426C>A r.(?) p.(Asp142Glu)


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