Variant #0000852119 (NC_000009.11:g.131388089C>T, NM_001130438.2:c.6111C>T (SPTAN1))

Chromosome 9
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.131388089C>T
DNA change (hg38) -
Published as SPTAN1(NM_001130438.2):c.6111C>T (p.G2037=), SPTAN1(NM_001363759.1):c.6111C>T (p.G2037=)
ISCN -
DB-ID WDR34_000074 See all 2 reported entries
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) 0.00233 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 2022-05-09 15:40:45 +02:00 (CEST)
Date last edited 2025-07-08 13:22:38 +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.6111C>T r.(?) p.(Gly2037=)
WDR34 NM_052844.3 -?/. - c.*7934G>A r.(=) p.(=)


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