Variant #0001037200 (NC_000009.11:g.131353848G>T, NM_001130438.2:c.3099G>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.131353848G>T
DNA change (hg38) -
Published as SPTAN1(NM_001130438.2):c.3099G>T (p.(Glu1033Asp), p.E1033D), SPTAN1(NM_001130438.3):c.3099G>T (p.E1033D)
ISCN -
DB-ID SPTAN1_000014 See all 4 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) 4.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SPTAN1 NM_001130438.2 -?/. - c.3099G>T r.(?) p.(Glu1033Asp)
WDR34 NM_052844.3 -?/. - c.*42175C>A r.(=) p.(=)


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