Variant #0001076108 (NC_000009.11:g.101594190G>T, NM_024642.4:c.868G>T (GALNT12))

Chromosome 9
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.101594190G>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID GALNT12_000023 See all 3 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs371949942
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 9.0E-5 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2026-05-07 14:46:01 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GALNT12 NM_024642.4 ?/. - c.868G>T r.(?) p.(Val290Phe)


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