Variant #0000554445 (NC_000015.9:g.44955823G>C, NM_025137.3:c.23C>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.44955823G>C
DNA change (hg38) g.44663625G>C
Published as SPG11(NM_025137.4):c.23C>G (p.A8G)
ISCN -
DB-ID SPG11_000103 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) 6.0E-5 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +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     
PATL2 NM_001145112.1 -?/. - c.*2328C>G r.(=) p.(=)
EIF3J NM_003758.2 -?/. - c.*102476G>C r.(=) p.(=)
SPG11 NM_025137.3 -?/. - c.23C>G r.(?) p.(Ala8Gly)


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