Variant #0001025579 (NC_000009.11:g.123751971G>A, NM_001735.2:c.3029C>T (C5))

Chromosome 9
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.123751971G>A
DNA change (hg38) -
Published as C5(NM_001317163.1):c.3047C>T (p.A1016V), C5(NM_001735.2):c.3029C>T (p.A1010V), C5(NM_001735.3):c.3029C>T (p.A1010V)
ISCN -
DB-ID C5_000005 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) 0.00067 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2025-02-07 18:57:27 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C5 NM_001735.2 -?/. - c.3029C>T r.(?) p.(Ala1010Val)


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