Variant #0000624629 (NC_000023.10:g.47483756T>C, NM_006950.3:c.-4629A>G (SYN1))

Chromosome X
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.47483756T>C
DNA change (hg38) g.47624357T>C
Published as CFP(NM_002621.2):c.1328A>G (p.Q443R)
ISCN -
DB-ID SYN1_000075
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) 2.0E-5 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 2019-12-06 12:43:26 +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.*52900T>C r.(=) p.(=)
CFP NM_002621.2 ?/. - c.1328A>G r.(?) p.(Gln443Arg)
TIMP1 NM_003254.2 ?/. - c.*37666T>C r.(=) p.(=)
SYN1 NM_006950.3 ?/. - c.-4629A>G r.(?) p.(=)


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