Variant #0000622339 (NC_000010.10:g.118891967_118891970del, NM_001112704.1:c.*1551_*1554del (VAX1))

Chromosome 10
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.118891967_118891970del
DNA change (hg38) g.117132456_117132459del
Published as VAX1(NM_199131.2):c.450_453delTGAA (p.E151Dfs*6)
ISCN -
DB-ID VAX1_000002
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-06 12:43:26 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
VAX1 NM_001112704.1 +/. - c.*1551_*1554del r.(=) p.(=)


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