Variant #0000618692 (NC_000023.10:g.100652922G>C, NM_000169.2:c.1165C>G (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.100652922G>C
DNA change (hg38) g.101397934G>C
Published as GLA(NM_000169.2):c.1165C>G (p.P389A)
ISCN -
DB-ID HNRNPH2_000006 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_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 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.1165C>G r.(?) p.(Pro389Ala)
RPL36A-HNRNPH2 NM_001199973.1 ?/. - c.408+2477G>C r.(=) p.(=)
HNRNPH2 NM_019597.4 ?/. - c.-10439G>C r.(?) p.(=)
RPL36A NM_021029.5 ?/. - c.*2186G>C r.(=) p.(=)


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