Variant #0000334346 (NC_000023.10:g.55034116C>T, NM_000032.4:c.*1497G>A (ALAS2))

Chromosome X
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.55034116C>T
DNA change (hg38) g.55007683C>T
Published as APEX2(NM_014481.3):c.*248C>T (p.(=))
ISCN -
DB-ID APEX2_000006
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +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.*1497G>A r.(=) p.(=)
APEX2 NM_014481.2 ?/. - c.*248C>T r.(=) p.(=)


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