Variant #0000998297 (NC_000010.10:g.45486414A>G, NM_007021.3:c.-12374T>C (C10orf10))

Chromosome 10
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.45486414A>G
DNA change (hg38) -
Published as RASSF4(NM_032023.3):c.704A>G (p.(Asp235Gly))
ISCN -
DB-ID C10orf10_000003
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) 0.00014 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     
C10orf25 NM_001039380.2 ?/. - c.*9412T>C r.(=) p.(=)
ZNF22 NM_006963.4 ?/. - c.-10102A>G r.(?) p.(=)
C10orf10 NM_007021.3 ?/. - c.-12374T>C r.(?) p.(=)
RASSF4 NM_032023.3 ?/. - c.704A>G r.(?) p.(Asp235Gly)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.