Variant #0000348325 (NC_000003.11:g.151055862G>T, NC_000003.11(NM_053002.4):c.2146-11985G>T (MED12L))

Chromosome 3
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.151055862G>T
DNA change (hg38) g.151338074G>T
Published as P2RY12(NM_022788.4):c.772C>A (p.P258T)
ISCN -
DB-ID MED12L_000004 See all 2 reported entries
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GPR171 NM_013308.3 +/. - c.-135114C>A r.(?) p.(=)
P2RY14 NM_014879.3 +/. - c.-59920C>A r.(?) p.(=)
P2RY12 NM_022788.3 +/. - c.772C>A r.(?) p.(Pro258Thr)
GPR87 NM_023915.3 +/. - c.-21587C>A r.(?) p.(=)
MED12L NM_053002.4 +/. - c.2146-11985G>T r.(=) p.(=)
P2RY13 NM_176894.2 +/. - c.-8546C>A r.(?) p.(=)
IGSF10 NM_178822.4 +/. - c.*98615C>A r.(=) p.(=)


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