Variant #0000538896 (NC_000010.10:g.102749620T>C, NM_021830.4:c.1463T>C (C10orf2))

Chromosome 10
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.102749620T>C
DNA change (hg38) g.100989863T>C
Published as C10orf2(NM_001163812.1):c.1463T>C (p.(Phe488Ser))
ISCN -
DB-ID C10orf2_000043
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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.*5732T>C r.(=) p.(=)
C10orf2 NM_021830.4 ?/. - c.1463T>C r.(?) p.(Phe488Ser)
MRPL43 NM_032112.2 ?/. - c.-2420A>G r.(?) p.(=)


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