Variant #0000314239 (NC_000023.10:g.47433684T>C, NM_006950.3:c.1699A>G (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.47433684T>C
DNA change (hg38) g.47574285T>C
Published as SYN1(NM_006950.3):c.1699A>G (p.T567A, p.(Thr567Ala)), SYN1(NM_133499.2):c.1699A>G (p.T567A)
ISCN -
DB-ID SYN1_000024 See all 5 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) 0.00121 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 2018-01-15 20:58:59 +01:00 (CET)
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.*2828T>C r.(=) p.(=)
TIMP1 NM_003254.2 -?/. - c.-8198T>C r.(?) p.(=)
SYN1 NM_006950.3 -?/. - c.1699A>G r.(?) p.(Thr567Ala)


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