Variant #0000896250 (NC_000023.10:g.47433597C>A, NM_006950.3:c.1786G>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.47433597C>A
DNA change (hg38) -
Published as SYN1(NM_133499.2):c.1786G>T (p.G596C)
ISCN -
DB-ID SYN1_000095
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-11-01 13:41:49 +01:00 (CET)
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.*2741C>A r.(=) p.(=)
TIMP1 NM_003254.2 ?/. - c.-8285C>A r.(?) p.(=)
SYN1 NM_006950.3 ?/. - c.1786G>T r.(?) p.(Gly596Cys)


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