Variant #0000545339 (NC_000011.9:g.66618369G>A, NM_001040716.1:c.2249C>T (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.66618369G>A
DNA change (hg38) g.66850898G>A
Published as PC(NM_001040716.1):c.2249C>T (p.T750M)
ISCN -
DB-ID C11orf80_000018
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) 0.00152 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 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PC NM_001040716.1 -/. - c.2249C>T r.(?) p.(Thr750Met)
RCE1 NM_005133.2 -/. - c.*4803G>A r.(=) p.(=)
LRFN4 NM_024036.4 -/. - c.-6847G>A r.(?) p.(=)
C11orf80 NM_024650.3 -/. - c.*7664G>A r.(=) p.(=)


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