Variant #0000659329 (NC_000023.10:g.47478976G>C, NM_006950.3:c.152C>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.47478976G>C
DNA change (hg38) g.47619577G>C
Published as SYN1(NM_006950.3):c.152C>G (p.(Ala51Gly))
ISCN -
DB-ID SYN1_000079
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) 0.00263 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2020-03-23 16:13:27 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARAF NM_001256196.1 -?/. - c.*48120G>C r.(=) p.(=)
CFP NM_002621.2 -?/. - c.*4698C>G r.(=) p.(=)
TIMP1 NM_003254.2 -?/. - c.*32886G>C r.(=) p.(=)
SYN1 NM_006950.3 -?/. - c.152C>G r.(?) p.(Ala51Gly)


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