Variant #0000618701 (NC_000023.10:g.100653895G>A, NM_000169.2:c.679C>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.100653895G>A
DNA change (hg38) g.101398907G>A
Published as GLA(NM_000169.3):c.679C>T (p.R227*)
ISCN -
DB-ID GLA_000577 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) Retrieve
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-12-04 15:24:38 +01:00 (CET)
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.679C>T r.(?) p.(Arg227Ter)
RPL36A-HNRNPH2 NM_001199973.1 +/. - c.408+3450G>A r.(=) p.(=)
HNRNPH2 NM_019597.4 +/. - c.-9466G>A r.(?) p.(=)
RPL36A NM_021029.5 +/. - c.*3159G>A r.(=) p.(=)


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