Variant #0000576139 (NC_000023.10:g.47433445T>G, NM_006950.3:c.1938A>C (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.47433445T>G
DNA change (hg38) g.47574046T>G
Published as SYN1(NM_006950.3):c.1938A>C (p.P646=)
ISCN -
DB-ID SYN1_000058
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-19 20:05:48 +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.*2589T>G r.(=) p.(=)
TIMP1 NM_003254.2 -?/. - c.-8437T>G r.(?) p.(=)
SYN1 NM_006950.3 -?/. - c.1938A>C r.(?) p.(Pro646=)


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