Variant #0000545337 (NC_000011.9:g.66617727A>G, NM_001040716.1:c.2682T>C (PC))

Chromosome 11
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.66617727A>G
DNA change (hg38) g.66850256A>G
Published as PC(NM_001040716.1):c.2682T>C (p.Y894=)
ISCN -
DB-ID C11orf80_000016
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) 0.00132 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-01 09:39:22 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PC NM_001040716.1 -/. - c.2682T>C r.(?) p.(Tyr894=)
RCE1 NM_005133.2 -/. - c.*4161A>G r.(=) p.(=)
LRFN4 NM_024036.4 -/. - c.-7489A>G r.(?) p.(=)
C11orf80 NM_024650.3 -/. - c.*7022A>G r.(=) p.(=)


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