Variant #0000281046 (NC_000023.10:g.100652969C>T, NM_000169.2:c.1118G>A (GLA))

Chromosome X
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.100652969C>T
DNA change (hg38) g.101397981C>T
Published as GLA(NM_000169.3):c.1118G>A (p.G373D)
ISCN -
DB-ID GLA_000397 See all 2 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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +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.1118G>A r.(?) p.(Gly373Asp)
RPL36A-HNRNPH2 NM_001199973.1 +?/. - c.408+2524C>T r.(=) p.(=)
HNRNPH2 NM_019597.4 +?/. - c.-10392C>T r.(?) p.(=)
RPL36A NM_021029.5 +?/. - c.*2233C>T r.(=) p.(=)


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