Variant #0000329670 (NC_000003.11:g.151107838T>A, NM_053002.4:c.5418T>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.151107838T>A
DNA change (hg38) g.151390050T>A
Published as MED12L(NM_053002.5):c.5418T>A (p.(His1806Gln))
ISCN -
DB-ID MED12L_000006
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) 3.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +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.-187090A>T r.(?) p.(=)
P2RY14 NM_014879.3 -?/. - c.-111896A>T r.(?) p.(=)
GPR87 NM_023915.3 -?/. - c.-73563A>T r.(?) p.(=)
MED12L NM_053002.4 -?/. - c.5418T>A r.(?) p.(His1806Gln)
P2RY13 NM_176894.2 -?/. - c.-60522A>T r.(?) p.(=)
IGSF10 NM_178822.4 -?/. - c.*46639A>T r.(=) p.(=)


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