Variant #0001027504 (NC_000023.10:g.47426757C>T, NM_006950.3:c.*5506G>A (SYN1))

Chromosome X
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.47426757C>T
DNA change (hg38) -
Published as ARAF(NM_001256196.2):c.1011C>T (p.A337=)
ISCN -
DB-ID SYN1_000100
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) 0.00405 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 2025-02-07 18:57:27 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARAF NM_001256196.1 -/. - c.1011C>T r.(?) p.(=)
TIMP1 NM_003254.2 -/. - c.-15125C>T r.(?) p.(=)
SYN1 NM_006950.3 -/. - c.*5506G>A r.(=) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.