Variant #0000289532 (NC_000003.11:g.151171421G>A, NM_053002.4:c.*20829G>A (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.151171421G>A
DNA change (hg38) g.151453633G>A
Published as IGSF10(NM_178822.4):c.466C>T (p.R156C)
ISCN -
DB-ID IGSF10_000009
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) 0.00012 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 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     
MED12L NM_053002.4 ?/. - c.*20829G>A r.(=) p.(=)
IGSF10 NM_178822.4 ?/. - c.466C>T r.(?) p.(Arg156Cys)


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