Variant #0000572596 (NC_000023.10:g.100656671_100656672insGA, NM_000169.2:c.495_496insTC (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.100656671_100656672insGA
DNA change (hg38) g.101401683_101401684insGA
Published as GLA(NM_000169.2):c.495_496insTC (p.L166Sfs*3)
ISCN -
DB-ID HNRNPH2_000018
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-20 18:13:23 +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.495_496insTC r.(?) p.(Leu166SerfsTer3)
RPL36A-HNRNPH2 NM_001199973.1 ?/. - c.408+6226_408+6227insGA r.(=) p.(=)
HNRNPH2 NM_019597.4 ?/. - c.-6690_-6689insGA r.(?) p.(=)
RPL36A NM_021029.5 ?/. - c.*5935_*5936insGA r.(=) p.(=)


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