Variant #0000506614 (NC_000001.10:g.24130889C>G, NC_000001.10(NM_000191.2):c.876+1G>C (HMGCL))

Chromosome 1
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.24130889C>G
DNA change (hg38) g.23804399C>G
Published as -
ISCN -
DB-ID HMGCL_000014 See all 7 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2022-03-17 16:35:36 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HMGCL NM_000191.2 +/. - c.876+1G>C r.spl? p.?
GALE NM_000403.3 +/. - c.-4089G>C r.(?) p.(=)


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