Variant #0000328445 (NC_000020.10:g.44485954_44485957dup, NM_080752.3:c.-511_-508dup (ZSWIM3))

Chromosome 20
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.44485954_44485957dup
DNA change (hg38) g.45857315_45857318dup
Published as ACOT8(NM_005469.3):c.2_3insAGAT (p.(Met1IlefsTer?))
ISCN -
DB-ID ACOT8_000001
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 2020-07-16 17:43:06 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ACOT8 NM_005469.3 ?/. - c.-2_2dup r.(?) p.(Met1?)
SNX21 NM_033421.2 ?/. - c.*16002_*16005dup r.(=) p.(=)
ZSWIM3 NM_080752.3 ?/. - c.-511_-508dup r.(?) p.(=)


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