Variant #0000539902 (NC_000010.10:g.45485168G>C, NM_007021.3:c.-11128C>G (C10orf10))

Chromosome 10
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.45485168G>C
DNA change (hg38) g.44989720G>C
Published as RASSF4(NM_032023.3):c.684G>C (p.(=))
ISCN -
DB-ID C10orf10_000001
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 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-26 14:23:52 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C10orf25 NM_001039380.2 -?/. - c.*10658C>G r.(=) p.(=)
ZNF22 NM_006963.4 -?/. - c.-11348G>C r.(?) p.(=)
C10orf10 NM_007021.3 -?/. - c.-11128C>G r.(?) p.(=)
RASSF4 NM_032023.3 -?/. - c.684G>C r.(?) p.(Gly228=)


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