Variant #0001052490 (NC_000006.11:g.131902491_131902494dup, NM_000045.3:c.438_441dup (ARG1))

Chromosome 6
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.131902491_131902494dup
DNA change (hg38) -
Published as ARG1(NM_000045.4):c.438_441dup (p.(Leu148Phefs*50))
ISCN -
DB-ID ARG1_000113
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 2025-11-01 13:22:20 +01:00 (CET)
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.438_441dup r.(?) p.(Leu148Phefs*50)
MED23 NM_004830.3 +?/. - c.*6327_*6330dup r.(=) p.(=)
MED23 NM_015979.3 +?/. - c.4095+6357_4095+6360dup r.(=) p.(=)


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