Variant #0000563683 (NC_000017.10:g.79479080A>G, NM_001077182.2:c.-16478A>G (FSCN2))

Chromosome 17
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.79479080A>G
DNA change (hg38) g.81512054A>G
Published as ACTG1(NM_001614.3):c.212T>C (p.(Ile71Thr))
ISCN -
DB-ID ACTG1_000101
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FSCN2 NM_001077182.2 +?/. - c.-16478A>G r.(?) p.(=)
ACTG1 NM_001614.3 +?/. - c.212T>C r.(?) p.(Ile71Thr)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.