Variant #0000678752 (NC_000010.10:g.102748921C>G, NM_021830.4:c.954C>G (C10orf2))

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.102748921C>G
DNA change (hg38) -
Published as TWNK(NM_001163812.1):c.954C>G (p.A318=)
ISCN -
DB-ID C10orf2_000055
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) 4.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2020-09-15 15:50:26 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SEMA4G NM_017893.3 -?/. - c.*5033C>G r.(=) p.(=)
C10orf2 NM_021830.4 -?/. - c.954C>G r.(?) p.(Ala318=)
MRPL43 NM_032112.2 -?/. - c.-1721G>C r.(?) p.(=)


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