Variant #0000693237 (NC_000023.10:g.100653916G>A, NM_000169.2:c.658C>T (GLA))

Chromosome X
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.100653916G>A
DNA change (hg38) -
Published as GLA(NM_000169.2):c.658C>T (p.R220*), GLA(NM_000169.3):c.658C>T (p.R220*)
ISCN -
DB-ID GLA_000572 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) Retrieve
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GLA NM_000169.2 +/. - c.658C>T r.(?) p.(Arg220Ter)
RPL36A-HNRNPH2 NM_001199973.1 +/. - c.408+3471G>A r.(=) p.(=)
HNRNPH2 NM_019597.4 +/. - c.-9445G>A r.(?) p.(=)
RPL36A NM_021029.5 +/. - c.*3180G>A r.(=) p.(=)


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