Variant #0000554437 (NC_000015.9:g.44949329T>C, NM_025137.3:c.833A>G (SPG11))

Chromosome 15
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.44949329T>C
DNA change (hg38) g.44657131T>C
Published as SPG11(NM_025137.4):c.833A>G (p.N278S, p.(Asn278Ser))
ISCN -
DB-ID SPG11_000094 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) 0.00807 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EIF3J NM_003758.2 -?/. - c.*95982T>C r.(=) p.(=)
SPG11 NM_025137.3 -?/. - c.833A>G r.(?) p.(Asn278Ser)


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