Variant #0000538889 (NC_000010.10:g.102748606C>T, NM_021830.4:c.639C>T (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.102748606C>T
DNA change (hg38) g.100988849C>T
Published as C10orf2(NM_001163812.1):c.639C>T (p.G213=)
ISCN -
DB-ID C10orf2_000010 See all 2 reported entries
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) 0.00116 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-29 10:12:15 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SEMA4G NM_017893.3 -?/. - c.*4718C>T r.(=) p.(=)
C10orf2 NM_021830.4 -?/. - c.639C>T r.(?) p.(Gly213=)
MRPL43 NM_032112.2 -?/. - c.-1406G>A r.(?) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.