Variant #0000719254 (NC_000003.11:g.151085514C>T, NM_053002.4:c.3303C>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.151085514C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID GPR87_000005
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) 0.00294 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GPR171 NM_013308.3 -?/. - c.-164766G>A r.(?) p.(=)
P2RY14 NM_014879.3 -?/. - c.-89572G>A r.(?) p.(=)
P2RY12 NM_022788.3 -?/. - c.-180+16966G>A r.(=) p.(=)
GPR87 NM_023915.3 -?/. - c.-51239G>A r.(?) p.(=)
MED12L NM_053002.4 -?/. - c.3303C>T r.(?) p.(Asp1101=)
P2RY13 NM_176894.2 -?/. - c.-38198G>A r.(?) p.(=)
IGSF10 NM_178822.4 -?/. - c.*68963G>A r.(=) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.