Variant #0000656403 (NC_000010.10:g.102748203G>A, NM_021830.4:c.236G>A (C10orf2))

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.102748203G>A
DNA change (hg38) g.100988446G>A
Published as TWNK(NM_001163812.1):c.236G>A (p.R79Q)
ISCN -
DB-ID C10orf2_000054
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-03-23 16:13:27 +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     
SEMA4G NM_017893.3 ?/. - c.*4315G>A r.(=) p.(=)
C10orf2 NM_021830.4 ?/. - c.236G>A r.(?) p.(Arg79Gln)
MRPL43 NM_032112.2 ?/. - c.-1003C>T r.(?) p.(=)


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