Variant #0000311546 (NC_000009.11:g.131360750C>T, NM_001130438.2:c.3486C>T (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.131360750C>T
DNA change (hg38) g.128598471C>T
Published as SPTAN1(NM_001130438.3):c.3486C>T (p.L1162=)
ISCN -
DB-ID SPTAN1_000032 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) 0.80499 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.3486C>T r.(?) p.(Leu1162=)
WDR34 NM_052844.3 -/. - c.*35273G>A r.(=) p.(=)


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