Variant #0000527194 (NC_000006.11:g.131904627A>C, NM_000045.3:c.798A>C (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.131904627A>C
DNA change (hg38) g.131583487A>C
Published as ARG1(NM_001244438.2):c.822A>C (p.K274N), MED23(NM_015979.4):c.4095+4222T>G
ISCN -
DB-ID ARG1_000016 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) 0.0001 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +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.798A>C r.(?) p.(Lys266Asn)
MED23 NM_004830.3 ?/. - c.*4192T>G r.(=) p.(=)
MED23 NM_015979.3 ?/. - c.4095+4222T>G r.(=) p.(=)


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