Variant #0000572631 (NC_000023.10:g.100667592C>T, NM_000169.2:c.-4701G>A (GLA))

Chromosome X
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.100667592C>T
DNA change (hg38) g.101412604C>T
Published as HNRNPH2(NM_001032393.3):c.616C>T (p.R206W), HNRNPH2(NM_019597.4):c.616C>T (p.(Arg206Trp)), HNRNPH2(NM_019597.5):c.616C>T (p.R206W)
ISCN -
DB-ID HNRNPH2_000004 See all 4 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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-04-16 21:50:28 +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.-4701G>A r.(?) p.(=)
RPL36A-HNRNPH2 NM_001199973.1 +/. - c.*612C>T r.(=) p.(=)
HNRNPH2 NM_019597.4 +/. - c.616C>T r.(?) p.(Arg206Trp)
RPL36A NM_021029.5 +/. - c.*16856C>T r.(=) p.(=)


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