Variant #0000284657 (NC_000023.10:g.100653883C>T, NM_000169.2:c.691G>A (GLA))

Chromosome X
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.100653883C>T
DNA change (hg38) g.101398895C>T
Published as GLA(NM_000169.2):c.691G>A (p.D231N)
ISCN -
DB-ID GLA_000061 See all 3 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_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)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GLA NM_000169.2 ?/. - c.691G>A r.(?) p.(Asp231Asn)
RPL36A-HNRNPH2 NM_001199973.1 ?/. - c.408+3438C>T r.(=) p.(=)
HNRNPH2 NM_019597.4 ?/. - c.-9478C>T r.(?) p.(=)
RPL36A NM_021029.5 ?/. - c.*3147C>T r.(=) p.(=)


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