Variant #0000618696 (NC_000023.10:g.100653088_100653089insA, NC_000023.10(NM_000169.2):c.1000-2_1000-1insT (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.100653088_100653089insA
DNA change (hg38) g.101398100_101398101insA
Published as -
ISCN -
DB-ID HNRNPH2_000033
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-07-20 18:06:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GLA NM_000169.2 +?/. - c.1000-2_1000-1insT r.spl? p.?
RPL36A-HNRNPH2 NM_001199973.1 +?/. - c.408+2643_408+2644insA r.(=) p.(=)
HNRNPH2 NM_019597.4 +?/. - c.-10273_-10272insA r.(?) p.(=)
RPL36A NM_021029.5 +?/. - c.*2352_*2353insA r.(=) p.(=)


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