Variant #0000866936 (NC_000023.10:g.100662839A>G, NM_000169.2:c.53T>C (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.100662839A>G
DNA change (hg38) -
Published as GLA(NM_000169.2):c.53T>C (p.F18S), GLA(NM_000169.3):c.53T>C (p.F18S)
ISCN -
DB-ID GLA_000096 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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2022-05-09 16:01:56 +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.53T>C r.(?) p.(Phe18Ser)
RPL36A-HNRNPH2 NM_001199973.1 +/. - c.409-4085A>G r.(=) p.(=)
HNRNPH2 NM_019597.4 +/. - c.-522A>G r.(?) p.(=)
RPL36A NM_021029.5 +/. - c.*12103A>G r.(=) p.(=)


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