Variant #0000349918 (NC_000003.11:g.150845649A>G, NM_053002.4:c.434A>G (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.150845649A>G
DNA change (hg38) g.151127862A>G
Published as -
ISCN -
DB-ID MED12L_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) 1.0E-5 View details
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 2020-03-23 16:13:27 +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.*70565T>C r.(=) p.(=)
P2RY14 NM_014879.3 -?/. - c.*85439T>C r.(=) p.(=)
GPR87 NM_023915.3 -?/. - c.*166308T>C r.(=) p.(=)
MED12L NM_053002.4 -?/. - c.434A>G r.(?) p.(Tyr145Cys)
P2RY13 NM_176894.2 -?/. - c.*200130T>C r.(=) p.(=)
IGSF10 NM_178822.4 -?/. - c.*308828T>C r.(=) p.(=)


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