Variant #0000329668 (NC_000003.11:g.150840682C>T, NM_053002.4:c.317C>T (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.150840682C>T
DNA change (hg38) g.151122895C>T
Published as MED12L(NM_053002.4):c.317C>T (p.(Thr106Ile))
ISCN -
DB-ID MED12L_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) Retrieve
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 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.*75532G>A r.(=) p.(=)
P2RY14 NM_014879.3 ?/. - c.*90406G>A r.(=) p.(=)
GPR87 NM_023915.3 ?/. - c.*171275G>A r.(=) p.(=)
MED12L NM_053002.4 ?/. - c.317C>T r.(?) p.(Thr106Ile)
P2RY13 NM_176894.2 ?/. - c.*205097G>A r.(=) p.(=)
IGSF10 NM_178822.4 ?/. - c.*313795G>A r.(=) p.(=)


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