Variant #0000998296 (NC_000010.10:g.45484728G>A, NM_007021.3:c.-10688C>T (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.45484728G>A
DNA change (hg38) -
Published as RASSF4(NM_032023.3):c.538G>A (p.(Val180Met))
ISCN -
DB-ID C10orf10_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) 5.0E-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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C10orf25 NM_001039380.2 ?/. - c.*11098C>T r.(=) p.(=)
ZNF22 NM_006963.4 ?/. - c.-11788G>A r.(?) p.(=)
C10orf10 NM_007021.3 ?/. - c.-10688C>T r.(?) p.(=)
RASSF4 NM_032023.3 ?/. - c.538G>A r.(?) p.(Val180Met)


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