Variant #0000653975 (NC_000001.10:g.24131018A>G, NC_000001.10(NM_000191.2):c.751-3T>C (HMGCL))

Chromosome 1
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.24131018A>G
DNA change (hg38) g.23804528A>G
Published as HMGCL(NM_000191.2):c.751-3T>C
ISCN -
DB-ID HMGCL_000015
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) 0 View details
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 2022-03-17 16:36:00 +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.751-3T>C r.spl? p.?
GALE NM_000403.3 -?/. - c.-4218T>C r.(?) p.(=)


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