Variant #0000659016 (NC_000023.10:g.100662869A>T, NM_000169.2:c.23T>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.100662869A>T
DNA change (hg38) g.101407881A>T
Published as GLA(NM_000169.2):c.23T>A (p.L8Q)
ISCN -
DB-ID HNRNPH2_000036
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 2020-03-23 16:13:27 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GLA NM_000169.2 -?/. - c.23T>A r.(?) p.(Leu8Gln)
RPL36A-HNRNPH2 NM_001199973.1 -?/. - c.409-4055A>T r.(=) p.(=)
HNRNPH2 NM_019597.4 -?/. - c.-492A>T r.(?) p.(=)
RPL36A NM_021029.5 -?/. - c.*12133A>T r.(=) p.(=)


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