Variant #0000979784 (NC_000011.9:g.66618678T>C, NM_001040716.1:c.2056A>G (PC))

Chromosome 11
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.66618678T>C
DNA change (hg38) -
Published as PC(NM_001040716.2):c.2056A>G (p.(Met686Val))
ISCN -
DB-ID C11orf80_000031
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +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     
PC NM_001040716.1 ?/. - c.2056A>G r.(?) p.(Met686Val)
RCE1 NM_005133.2 ?/. - c.*5112T>C r.(=) p.(=)
LRFN4 NM_024036.4 ?/. - c.-6538T>C r.(?) p.(=)
C11orf80 NM_024650.3 ?/. - c.*7973T>C r.(=) p.(=)


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