Variant #0000682462 (NC_000023.10:g.47435625G>A, NM_006950.3:c.1063C>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.47435625G>A
DNA change (hg38) -
Published as SYN1(NM_006950.3):c.1063C>T (p.L355=)
ISCN -
DB-ID SYN1_000082
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) 0.00021 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2020-09-15 15:50:26 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARAF NM_001256196.1 -?/. - c.*4769G>A r.(=) p.(=)
TIMP1 NM_003254.2 -?/. - c.-6257G>A r.(?) p.(=)
SYN1 NM_006950.3 -?/. - c.1063C>T r.(?) p.(Leu355=)


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