Variant #0000998053 (NC_000010.10:g.102749087C>T, NM_021830.4:c.1120C>T (C10orf2))

Chromosome 10
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.102749087C>T
DNA change (hg38) -
Published as TWNK(NM_021830.5):c.1120C>T (p.R374W)
ISCN -
DB-ID C10orf2_000041
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
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     
SEMA4G NM_017893.3 +?/. - c.*5199C>T r.(=) p.(=)
C10orf2 NM_021830.4 +?/. - c.1120C>T r.(?) p.(Arg374Trp)
MRPL43 NM_032112.2 +?/. - c.-1887G>A r.(?) p.(=)


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