Variant #0000799238 (NC_000001.10:g.24125479C>G, NM_000191.2:c.*3474G>C (HMGCL))

Chromosome 1
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.24125479C>G
DNA change (hg38) -
Published as GALE(NM_000403.3):c.19G>C (p.V7L)
ISCN -
DB-ID GALE_000011
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 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HMGCL NM_000191.2 ?/. - c.*3474G>C r.(=) p.(=)
GALE NM_000403.3 ?/. - c.19G>C r.(?) p.(Val7Leu)
LYPLA2 NM_007260.2 ?/. - c.*4257C>G r.(=) p.(=)


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