Variant #0000888637 (NC_000009.11:g.131336978C>A, NM_001130438.2:c.388C>A (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.131336978C>A
DNA change (hg38) -
Published as SPTAN1(NM_001363759.2):c.388C>A (p.Q130K)
ISCN -
DB-ID WDR34_000078
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2022-11-01 13:01:21 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SPTAN1 NM_001130438.2 ?/. - c.388C>A r.(?) p.(Gln130Lys)
WDR34 NM_052844.3 ?/. - c.*59045G>T r.(=) p.(=)


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