Variant #0001078467 (NC_000023.10:g.55043925T>C, NM_000032.4:c.997A>G (ALAS2))

Chromosome X
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.55043925T>C
DNA change (hg38) -
Published as -
ISCN -
DB-ID ALAS2_000055
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2026-06-10 14:01:01 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ALAS2 NM_000032.4 +?/. - c.997A>G r.(?) p.(Met333Val)


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