Variant #0000993384 (NC_000003.11:g.151165532G>C, NM_053002.4:c.*14940G>C (MED12L))

Chromosome 3
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.151165532G>C
DNA change (hg38) -
Published as IGSF10(NM_178822.4):c.2237C>G (p.(Pro746Arg))
ISCN -
DB-ID IGSF10_000018
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) 0.00643 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +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     
MED12L NM_053002.4 +/. - c.*14940G>C r.(=) p.(=)
IGSF10 NM_178822.4 +/. - c.2237C>G r.(?) p.(Pro746Arg)


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