Variant #0000975632 (NC_000003.11:g.151129094G>T, NM_053002.4:c.5834G>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.151129094G>T
DNA change (hg38) -
Published as MED12L(NM_053002.6):c.5834G>T (p.G1945V)
ISCN -
DB-ID GPR87_000016
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 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GPR171 NM_013308.3 ?/. - c.-208346C>A r.(?) p.(=)
P2RY14 NM_014879.3 ?/. - c.-133152C>A r.(?) p.(=)
GPR87 NM_023915.3 ?/. - c.-94819C>A r.(?) p.(=)
MED12L NM_053002.4 ?/. - c.5834G>T r.(?) p.(Gly1945Val)
P2RY13 NM_176894.2 ?/. - c.-81778C>A r.(?) p.(=)
IGSF10 NM_178822.4 ?/. - c.*25383C>A r.(=) p.(=)


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