Variant #0000329676 (NC_000003.11:g.151164045A>T, NM_053002.4:c.*13453A>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.151164045A>T
DNA change (hg38) g.151446257A>T
Published as IGSF10(NM_178822.4):c.3724T>A (p.(Leu1242Ile))
ISCN -
DB-ID IGSF10_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) 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     
MED12L NM_053002.4 ?/. - c.*13453A>T r.(=) p.(=)
IGSF10 NM_178822.4 ?/. - c.3724T>A r.(?) p.(Leu1242Ile)


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