Variant #0000908396 (NC_000010.10:g.135176415G>A, NM_004092.3:c.830C>T (ECHS1))

Chromosome 10
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.135176415G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID ECHS1_000025
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs775650144
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-5 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2022-12-09 16:52:01 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ECHS1 NM_004092.3 +?/. - c.830C>T r.(?) p.(Thr277Ile)


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