Variant #0000689625 (NC_000006.11:g.131902519G>C, NC_000006.11(NM_000045.3):c.465+1G>C (ARG1))

Chromosome 6
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.131902519G>C
DNA change (hg38) -
Published as ARG1(NM_000045.4):c.465+1G>C
ISCN -
DB-ID ARG1_000030
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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2020-09-15 15:50:26 +02:00 (CEST)
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.465+1G>C r.spl? p.?
MED23 NM_004830.3 +/. - c.*6300C>G r.(=) p.(=)
MED23 NM_015979.3 +/. - c.4095+6330C>G r.(=) p.(=)


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