Variant #0000272224 (NC_000010.10:g.102748598C>G, NM_021830.4:c.631C>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.102748598C>G
DNA change (hg38) g.100988841C>G
Published as C10orf2(NM_001163812.1):c.631C>G (p.P211A)
ISCN -
DB-ID C10orf2_000019
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 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 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SEMA4G NM_017893.3 -?/. - c.*4710C>G r.(=) p.(=)
C10orf2 NM_021830.4 -?/. - c.631C>G r.(?) p.(Pro211Ala)
MRPL43 NM_032112.2 -?/. - c.-1398G>C r.(?) p.(=)


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