Variant #0000248611 (NC_000009.11:g.131346218A>C, NM_001130438.2:c.2163= (SPTAN1))

Chromosome 9
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.131346218A>C
DNA change (hg38) g.128583939A>C
Published as SPTAN1(NM_001130438.3):c.2163A>C (p.A721=)
ISCN -
DB-ID SPTAN1_000077
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) 0.99293 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +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.2163= r.(=) p.(Ala721=)
WDR34 NM_052844.3 -/. - c.*49805T>G r.(=) p.(=)


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