Variant #0000611886 (NC_000009.11:g.131398680C>T, NM_001130438.2:c.*3067C>T (SPTAN1))

Chromosome 9
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.131398680C>T
DNA change (hg38) g.128636401C>T
Published as WDR34(NM_052844.3):c.583G>A (p.V195M)
ISCN -
DB-ID WDR34_000038
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) 5.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-04 15:24:38 +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     
SPTAN1 NM_001130438.2 ?/. - c.*3067C>T r.(=) p.(=)
WDR34 NM_052844.3 ?/. - c.583G>A r.(?) p.(Val195Met)


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