Variant #0000803895 (NC_000009.11:g.131341997T>G, NM_001130438.2:c.1303T>G (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.131341997T>G
DNA change (hg38) -
Published as SPTAN1(NM_001130438.2):c.1303T>G (p.S435A), SPTAN1(NM_001130438.3):c.1303T>G (p.S435A)
ISCN -
DB-ID SPTAN1_000010 See all 12 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) 0.00225 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 2021-09-17 14:40:49 +02:00 (CEST)
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.1303T>G r.(?) p.(Ser435Ala)
WDR34 NM_052844.3 -?/. - c.*54026A>C r.(=) p.(=)


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