Variant #0000249024 (NC_000003.11:g.151056598A>C, NC_000003.11(NM_053002.4):c.2146-11249A>C (MED12L))

Chromosome 3
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.151056598A>C
DNA change (hg38) g.151338810A>C
Published as MED12L(NM_053002.6):c.2146-11249A>C, P2RY12(NM_022788.5):c.36T>G (p.G12=)
ISCN -
DB-ID MED12L_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) 0.8681 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GPR171 NM_013308.3 -/. - c.-135850T>G r.(?) p.(=)
P2RY14 NM_014879.3 -/. - c.-60656T>G r.(?) p.(=)
P2RY12 NM_022788.3 -/. - c.36T>G r.(?) p.(Gly12=)
GPR87 NM_023915.3 -/. - c.-22323T>G r.(?) p.(=)
MED12L NM_053002.4 -/. - c.2146-11249A>C r.(=) p.(=)
P2RY13 NM_176894.2 -/. - c.-9282T>G r.(?) p.(=)
IGSF10 NM_178822.4 -/. - c.*97879T>G r.(=) p.(=)


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