Variant #0000248564 (NC_000006.11:g.131914232A>G, NM_000045.3:c.*9184A>G (ARG1))

Chromosome 6
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.131914232A>G
DNA change (hg38) g.131593092A>G
Published as MED23(NM_004830.4):c.3312T>C (p.A1104=)
ISCN -
DB-ID MED23_000002 See all 2 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) 0.02311 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARG1 NM_000045.3 -/. - c.*9184A>G r.(=) p.(=)
MED23 NM_004830.3 -/. - c.3312T>C r.(?) p.(Ala1104=)
MED23 NM_015979.3 -/. - c.3330T>C r.(?) p.(Ala1110=)


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