Variant #0000284658 (NC_000023.10:g.100653857T>C, NM_000169.2:c.717A>G (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.100653857T>C
DNA change (hg38) g.101398869T>C
Published as GLA(NM_000169.2):c.717A>G (p.I239M)
ISCN -
DB-ID GLA_000685
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GLA NM_000169.2 -?/. - c.717A>G r.(?) p.(Ile239Met)
RPL36A-HNRNPH2 NM_001199973.1 -?/. - c.408+3412T>C r.(=) p.(=)
HNRNPH2 NM_019597.4 -?/. - c.-9504T>C r.(?) p.(=)
RPL36A NM_021029.5 -?/. - c.*3121T>C r.(=) p.(=)


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