Variant #0000923092 (NC_000001.10:g.228285553G>T, NM_001658.3:c.385G>T (ARF1))

Chromosome 1
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.228285553G>T
DNA change (hg38) -
Published as ARF1(NM_001024226.2):c.385G>T (p.D129Y)
ISCN -
DB-ID ARF1_000003
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-04-16 21:50:28 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARF1 NM_001658.3 ?/. - c.385G>T r.(?) p.(Asp129Tyr)
C1orf35 NM_024319.2 ?/. - c.*3279C>A r.(=) p.(=)


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