Variant #0000517266 (NC_000002.11:g.99766944A>T, NC_000002.11(NM_144706.2):c.27-2A>T (C2orf15))

Chromosome 2
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.99766944A>T
DNA change (hg38) g.99150481A>T
Published as C2orf15(NM_144706.2):c.27-2A>T (p.?)
ISCN -
DB-ID C2orf15_000006
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) 3.0E-5 View details
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 2020-06-09 09:13:12 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LIPT1 NM_015929.3 -?/. - c.-4698A>T r.(?) p.(=)
C2orf15 NM_144706.2 -?/. - c.27-2A>T r.spl? p.?
TSGA10 NM_182911.3 -?/. - c.-9538T>A r.(?) p.(=)


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