Variant #0000984703 (NC_000023.10:g.47433732_47433735dup, NM_006950.3:c.1648_1651dup (SYN1))

Chromosome X
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.47433732_47433735dup
DNA change (hg38) -
Published as SYN1(NM_006950.3):c.1648_1651dup (p.(Ser551CysfsTer134))
ISCN -
DB-ID SYN1_000097
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARAF NM_001256196.1 +?/. - c.*2876_*2879dup r.(=) p.(=)
TIMP1 NM_003254.2 +?/. - c.-8150_-8147dup r.(?) p.(=)
SYN1 NM_006950.3 +?/. - c.1648_1651dup r.(?) p.(Ser551Cysfs*134)


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