Variant #0000288389 (NC_000023.10:g.100653420C>A, NM_000169.2:c.937G>T (GLA))

Chromosome X
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.100653420C>A
DNA change (hg38) g.101398432C>A
Published as GLA(NM_000169.2):c.937G>T (p.D313Y, p.(Asp313Tyr)), GLA(NM_000169.3):c.937G>T (p.D313Y), RPL36A-HNRNPH2(NM_001199973.2):c.300+2975C>A
ISCN -
DB-ID GLA_000001 See all 12 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) 0.00305 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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.937G>T r.(?) p.(Asp313Tyr)
RPL36A-HNRNPH2 NM_001199973.1 -/. - c.408+2975C>A r.(=) p.(=)
HNRNPH2 NM_019597.4 -/. - c.-9941C>A r.(?) p.(=)
RPL36A NM_021029.5 -/. - c.*2684C>A r.(=) p.(=)


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