Variant #0000576779 (NC_000023.10:g.55039960G>A, NM_000032.4:c.1559C>T (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.55039960G>A
DNA change (hg38) g.55013527G>A
Published as ALAS2(NM_000032.4):c.1559C>T (p.(Pro520Leu)), ALAS2(NM_000032.5):c.1559C>T (p.P520L)
ISCN -
DB-ID ALAS2_000012 See all 5 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) 0.00134 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +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.1559C>T r.(?) p.(Pro520Leu)


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