Variant #0000913202 (NC_000010.10:g.102750783C>A, NC_000010.10(NM_021830.4):c.1734+16C>A (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.102750783C>A
DNA change (hg38) -
Published as TWNK(NM_021830.5):c.1734+16C>A
ISCN -
DB-ID C10orf2_000071
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) 0.27271 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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SEMA4G NM_017893.3 -/. - c.*6895C>A r.(=) p.(=)
C10orf2 NM_021830.4 -/. - c.1734+16C>A r.(=) p.(=)
MRPL43 NM_032112.2 -/. - c.-3583G>T r.(?) p.(=)


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