Variant #0000659010 (NC_000023.10:g.100656740C>T, NM_000169.2:c.427G>A (GLA))

Chromosome X
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.100656740C>T
DNA change (hg38) g.101401752C>T
Published as GLA(NM_000169.2):c.427G>A (p.A143T), GLA(NM_000169.3):c.427G>A (p.A143T)
ISCN -
DB-ID GLA_000014 See all 9 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) 0.00054 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GLA NM_000169.2 -?/. - c.427G>A r.(?) p.(Ala143Thr)
RPL36A-HNRNPH2 NM_001199973.1 -?/. - c.408+6295C>T r.(=) p.(=)
HNRNPH2 NM_019597.4 -?/. - c.-6621C>T r.(?) p.(=)
RPL36A NM_021029.5 -?/. - c.*6004C>T r.(=) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.