Variant #0000980678 (NC_000013.10:g.36871782G>T, NM_001142294.1:c.*6720C>A (SPG20))

Chromosome 13
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.36871782G>T
DNA change (hg38) -
Published as CCDC169(NM_001144981.3):c.75C>A (p.(Val25=))
ISCN -
DB-ID CCDC169_000002
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) 0.00216 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SPG20 NM_001142294.1 -?/. - c.*6720C>A r.(=) p.(=)
CCDC169 NM_001144981.2 -?/. - c.75C>A r.(?) p.(=)
CCDC169-SOHLH2 NM_001198910.1 -?/. - c.-105C>A r.(?) p.(=)
SOHLH2 NM_017826.2 -?/. - c.-83119C>A r.(?) p.(=)


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