Variant #0000315952 (NC_000023.10:g.47464725C>T, NM_006950.3:c.581G>A (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.47464725C>T
DNA change (hg38) g.47605326C>T
Published as SYN1(NM_006950.3):c.581G>A (p.R194H)
ISCN -
DB-ID SYN1_000041
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 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARAF NM_001256196.1 ?/. - c.*33869C>T r.(=) p.(=)
TIMP1 NM_003254.2 ?/. - c.*18635C>T r.(=) p.(=)
SYN1 NM_006950.3 ?/. - c.581G>A r.(?) p.(Arg194His)


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