Variant #0000576788 (NC_000023.10:g.55054238C>T, NC_000023.10(NM_000032.4):c.-15-1790G>A (ALAS2))

Chromosome X
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.55054238C>T
DNA change (hg38) g.55027805C>T
Published as ALAS2(NM_000032.4):c.-15-1790G>A (p.(=)), ALAS2(NM_001037968.3):c.3G>A (p.M1?), ALAS2(NM_001037968.4):c.3G>A (p.M1?)
ISCN -
DB-ID ALAS2_000015 See all 4 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) 0.00285 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 2022-05-09 15:51:19 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ALAS2 NM_000032.4 -/. - c.-15-1790G>A r.(=) p.(=)


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