Variant #0000810429 (NC_000023.10:g.47433682T>A, NM_006950.3:c.1701A>T (SYN1))

Chromosome X
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.47433682T>A
DNA change (hg38) -
Published as SYN1(NM_006950.3):c.1701A>T (p.T567=), SYN1(NM_133499.2):c.1701A>T (p.T567=)
ISCN -
DB-ID SYN1_000087 See all 2 reported entries
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) 0.00022 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2022-11-01 13:01:21 +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.*2826T>A r.(=) p.(=)
TIMP1 NM_003254.2 -?/. - c.-8200T>A r.(?) p.(=)
SYN1 NM_006950.3 -?/. - c.1701A>T r.(?) p.(Thr567=)


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