Variant #0000559939 (NC_000016.9:g.89613070_89613078del, NM_003119.2:c.1454_1462del (SPG7))

Chromosome 16
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.89613070_89613078del
DNA change (hg38) g.89546662_89546670del
Published as SPG7(NM_001363850.1):c.1450-1_1457delGGAGAGGCG, SPG7(NM_003119.4):c.1450-1_1457delGGAGAGGCG, SPG7(NM_003119.4):c.1454_1462del (p.(Arg485_Glu487del))
ISCN -
DB-ID SPG7_000002 See all 8 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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2025-11-01 13:22:20 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RPL13 NM_000977.3 +/. - c.-14071_-14063del r.(?) p.(=)
SPG7 NM_003119.2 +/. - c.1454_1462del r.(?) p.(Arg485_Glu487del)


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