Variant #0000518313 (NC_000003.11:g.150874057G>T, NM_053002.4:c.666G>T (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.150874057G>T
DNA change (hg38) g.151156270G>T
Published as MED12L(NM_053002.5):c.666G>T (p.E222D)
ISCN -
DB-ID GPR87_000001
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) 0.00029 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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.*42157C>A r.(=) p.(=)
P2RY14 NM_014879.3 -?/. - c.*57031C>A r.(=) p.(=)
GPR87 NM_023915.3 -?/. - c.*137900C>A r.(=) p.(=)
MED12L NM_053002.4 -?/. - c.666G>T r.(?) p.(Glu222Asp)
P2RY13 NM_176894.2 -?/. - c.*171722C>A r.(=) p.(=)
IGSF10 NM_178822.4 -?/. - c.*280420C>A r.(=) p.(=)


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