Variant #0000307886 (NC_000010.10:g.102743776G>A, NM_021830.4:c.-4192G>A (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.102743776G>A
DNA change (hg38) g.100984019G>A
Published as SEMA4G(NM_017893.3):c.2420G>A (p.S807N)
ISCN -
DB-ID MRPL43_000002
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_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.2420G>A r.(?) p.(Ser807Asn)
C10orf2 NM_021830.4 -?/. - c.-4192G>A r.(?) p.(=)
MRPL43 NM_032112.2 -?/. - c.*2715C>T r.(=) p.(=)


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