Variant #0001053950 (NC_000011.9:g.66617690C>A, NC_000011.9(NM_001040716.1):c.2718+1G>T (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.66617690C>A
DNA change (hg38) -
Published as PC(NM_001040716.2):c.2718+1G>T
ISCN -
DB-ID C11orf80_000034
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 2025-11-01 13:22:20 +01:00 (CET)
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.2718+1G>T r.spl? p.?
RCE1 NM_005133.2 ?/. - c.*4124C>A r.(=) p.(=)
LRFN4 NM_024036.4 ?/. - c.-7526C>A r.(?) p.(=)
C11orf80 NM_024650.3 ?/. - c.*6985C>A r.(=) p.(=)


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