Variant #0001064088 (NC_000003.11:g.150803727A>T, NM_053002.4:c.-987A>T (MED12L))

Chromosome 3
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.150803727A>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID chr3_007572
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2026-01-20 18:57:21 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MED12L NM_001393769.1 -?/. - c.-130+4A>T r.spl? p.?
GPR171 NM_013308.3 -?/. - c.*112487T>A r.(=) p.(=)
P2RY14 NM_014879.3 -?/. - c.*127361T>A r.(=) p.(=)
GPR87 NM_023915.3 -?/. - c.*208230T>A r.(=) p.(=)
MED12L NM_053002.4 -?/. - c.-987A>T r.(?) p.(=)
P2RY13 NM_176894.2 -?/. - c.*242052T>A r.(=) p.(=)
IGSF10 NM_178822.4 -?/. - c.*350750T>A r.(=) p.(=)


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