Variant #0000619599 (NC_000023.10:g.47478989C>T, NM_006950.3:c.139G>A (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.47478989C>T
DNA change (hg38) g.47619590C>T
Published as SYN1(NM_006950.3):c.139G>A (p.G47R)
ISCN -
DB-ID SYN1_000074
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 2019-12-04 15:24:38 +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.*48133C>T r.(=) p.(=)
CFP NM_002621.2 -?/. - c.*4685G>A r.(=) p.(=)
TIMP1 NM_003254.2 -?/. - c.*32899C>T r.(=) p.(=)
SYN1 NM_006950.3 -?/. - c.139G>A r.(?) p.(Gly47Arg)


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