Variant #0000272246 (NC_000001.10:g.228290912C>A, NM_001658.3:c.*5198C>A (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.228290912C>A
DNA change (hg38) g.228103211C>A
Published as C1orf35(NM_024319.4):c.17G>T (p.R6L)
ISCN -
DB-ID C1orf35_000001
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-11-27 17:27:23 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARF1 NM_001658.3 ?/. - c.*5198C>A r.(=) p.(=)
C1orf35 NM_024319.2 ?/. - c.17G>T r.(?) p.(Arg6Leu)
MRPL55 NM_181441.2 ?/. - c.*3549G>T r.(=) p.(=)


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