Variant #0000328050 (NC_000002.11:g.203848315dup, NM_001104586.1:c.2146dup (ALS2CR8))

Chromosome 2
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.203848315dup
DNA change (hg38) g.202983592dup
Published as CARF(NM_001104586.1):c.2138_2139insA (p.(Thr716AsnfsTer5))
ISCN -
DB-ID ALS2CR8_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 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ALS2CR8 NM_001104586.1 ?/. - c.2146dup r.(?) p.(Thr716AsnfsTer5)
WDR12 NM_018256.3 ?/. - c.-72109dup r.(?) p.(=)


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