Variant #0001035475 (NC_000006.11:g.131946054G>A, NM_000045.3:c.*41006G>A (ARG1))

Chromosome 6
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.131946054G>A
DNA change (hg38) -
Published as MED23(NM_004830.4):c.235C>T (p.L79F, p.(Leu79Phe))
ISCN -
DB-ID MED23_000008 See all 4 reported entries
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) 0.00027 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 2025-05-05 21:14:00 +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     
ARG1 NM_000045.3 ?/. - c.*41006G>A r.(=) p.(=)
MED23 NM_004830.3 ?/. - c.235C>T r.(?) p.(Leu79Phe)
MED23 NM_015979.3 ?/. - c.235C>T r.(?) p.(Leu79Phe)


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