Variant #0000333921 (NC_000023.10:g.47426765T>C, NM_006950.3:c.*5498A>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.47426765T>C
DNA change (hg38) g.47567366T>C
Published as ARAF(NM_001256196.1):c.1019T>C (p.(Val340Ala))
ISCN -
DB-ID ARAF_000004
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +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.1019T>C r.(?) p.(Val340Ala)
TIMP1 NM_003254.2 ?/. - c.-15117T>C r.(?) p.(=)
SYN1 NM_006950.3 ?/. - c.*5498A>G r.(=) p.(=)


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