Variant #0001005545 (NC_000020.10:g.61458133C>G, NM_001853.3:c.753C>G (COL9A3))

Chromosome 20
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.61458133C>G
DNA change (hg38) -
Published as COL9A3(NM_001853.3):c.753C>G (p.(Phe251Leu)), COL9A3(NM_001853.4):c.753C>G (p.F251L)
ISCN -
DB-ID COL9A3_000109 See all 3 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) 4.0E-5 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 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COL9A3 NM_001853.3 ?/. - c.753C>G r.(?) p.(Phe251Leu)
TCFL5 NM_006602.2 ?/. - c.*15194G>C r.(=) p.(=)


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