Variant #0000523328 (NC_000004.11:g.80992755dup, NM_058172.5:c.207dup (ANTXR2))

Chromosome 4
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.80992755dup
DNA change (hg38) g.80071601dup
Published as ANTXR2(NM_058172.5):c.207dup (p.(Ala70CysfsTer8))
ISCN -
DB-ID ANTXR2_000022
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 2020-06-16 13:22:24 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ANTXR2 NM_058172.5 +?/. - c.207dup r.(?) p.(Ala70CysfsTer8)


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