Variant #0000691149 (NC_000011.9:g.66589136T>C, NM_024650.3:c.1359T>C (C11orf80))

Chromosome 11
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.66589136T>C
DNA change (hg38) -
Published as C11orf80(NM_024650.3):c.1359T>C (p.T453=)
ISCN -
DB-ID C11orf80_000022
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 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RCE1 NM_005133.2 -?/. - c.-21791T>C r.(?) p.(=)
C11orf80 NM_024650.3 -?/. - c.1359T>C r.(?) p.(Thr453=)


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