Variant #0000923856 (NC_000003.11:g.151055966G>A, NC_000003.11(NM_053002.4):c.2146-11881G>A (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.151055966G>A
DNA change (hg38) -
Published as P2RY12(NM_022788.4):c.668C>T (p.T223M)
ISCN -
DB-ID GPR87_000010
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) 5.0E-5 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-04-16 21:50:28 +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     
GPR171 NM_013308.3 -?/. - c.-135218C>T r.(?) p.(=)
P2RY14 NM_014879.3 -?/. - c.-60024C>T r.(?) p.(=)
P2RY12 NM_022788.3 -?/. - c.668C>T r.(?) p.(Thr223Met)
GPR87 NM_023915.3 -?/. - c.-21691C>T r.(?) p.(=)
MED12L NM_053002.4 -?/. - c.2146-11881G>A r.(=) p.(=)
P2RY13 NM_176894.2 -?/. - c.-8650C>T r.(?) p.(=)
IGSF10 NM_178822.4 -?/. - c.*98511C>T r.(=) p.(=)


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