Variant #0000913200 (NC_000010.10:g.102750623T>C, NC_000010.10(NM_021830.4):c.1593-3T>C (C10orf2))

Chromosome 10
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.102750623T>C
DNA change (hg38) -
Published as TWNK(NM_021830.5):c.1593-3T>C
ISCN -
DB-ID C10orf2_000069
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) 0.27267 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-01-11 15:44:22 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SEMA4G NM_017893.3 -/. - c.*6735T>C r.(=) p.(=)
C10orf2 NM_021830.4 -/. - c.1593-3T>C r.spl? p.?
MRPL43 NM_032112.2 -/. - c.-3423A>G r.(?) p.(=)


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