Variant #0000272221 (NC_000010.10:g.102750689T>C, NM_021830.4:c.1656T>C (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.102750689T>C
DNA change (hg38) g.100990932T>C
Published as C10orf2(NM_001163812.1):c.1656T>C (p.H552=)
ISCN -
DB-ID C10orf2_000023
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) 1.0E-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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-06-29 10:15:28 +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.*6801T>C r.(=) p.(=)
C10orf2 NM_021830.4 -?/. - c.1656T>C r.(?) p.(His552=)
MRPL43 NM_032112.2 -?/. - c.-3489A>G r.(?) p.(=)


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