Variant #0000885604 (NC_000003.11:g.151078278A>G, NM_053002.4:c.2737A>G (MED12L))

Chromosome 3
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.151078278A>G
DNA change (hg38) -
Published as MED12L(NM_053002.6):c.2737A>G (p.K913E)
ISCN -
DB-ID GPR87_000008
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 2022-11-01 13:01:21 +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.-157530T>C r.(?) p.(=)
P2RY14 NM_014879.3 ?/. - c.-82336T>C r.(?) p.(=)
P2RY12 NM_022788.3 ?/. - c.-179-19730T>C r.(=) p.(=)
GPR87 NM_023915.3 ?/. - c.-44003T>C r.(?) p.(=)
MED12L NM_053002.4 ?/. - c.2737A>G r.(?) p.(Lys913Glu)
P2RY13 NM_176894.2 ?/. - c.-30962T>C r.(?) p.(=)
IGSF10 NM_178822.4 ?/. - c.*76199T>C r.(=) p.(=)


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