Variant #0001033758 (NC_000003.11:g.151165106T>G, NM_053002.4:c.*14514T>G (MED12L))

Chromosome 3
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.151165106T>G
DNA change (hg38) -
Published as IGSF10(NM_178822.5):c.2663A>C (p.(Gln888Pro))
ISCN -
DB-ID IGSF10_000020
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) 0.00156 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MED12L NM_053002.4 ?/. - c.*14514T>G r.(=) p.(=)
IGSF10 NM_178822.4 ?/. - c.2663A>C r.(?) p.(Gln888Pro)


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