Variant #0000619597 (NC_000023.10:g.47436881G>A, NM_006950.3:c.794C>T (SYN1))

Chromosome X
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.47436881G>A
DNA change (hg38) g.47577482G>A
Published as -
ISCN -
DB-ID SYN1_000072
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARAF NM_001256196.1 ?/. - c.*6025G>A r.(=) p.(=)
TIMP1 NM_003254.2 ?/. - c.-5001G>A r.(?) p.(=)
SYN1 NM_006950.3 ?/. - c.794C>T r.(?) p.(Pro265Leu)


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