Variant #0000536426 (NC_000009.11:g.131396618_131396621dup, NM_001130438.2:c.*1005_*1008dup (SPTAN1))

Chromosome 9
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.131396618_131396621dup
DNA change (hg38) g.128634339_128634342dup
Published as WDR34(NM_052844.3):c.1256_1259dupTGTA (p.S421Vfs*40)
ISCN -
DB-ID WDR34_000024
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-25 18:50:07 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SPTAN1 NM_001130438.2 +?/. - c.*1005_*1008dup r.(=) p.(=)
WDR34 NM_052844.3 +?/. - c.1256_1259dup r.(?) p.(Ser421ValfsTer40)


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