Variant #0000965184 (NC_000009.11:g.131340457A>G, NM_001130438.2:c.1154A>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.131340457A>G
DNA change (hg38) -
Published as SPTAN1(NM_001130438.3):c.1154A>G (p.N385S)
ISCN -
DB-ID WDR34_000093
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) 5.0E-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 2024-02-26 20:06:56 +01:00 (CET)
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.1154A>G r.(?) p.(Asn385Ser)
WDR34 NM_052844.3 -?/. - c.*55566T>C r.(=) p.(=)


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