Variant #0001013184 (NC_000011.9:g.58920427C>T, NM_001312909.1:c.1286C>T (FAM111A))

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.58920427C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID FAM111A_000023
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs771954122
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-5 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2024-10-29 19:00:02 +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     
FAM111A NM_001312909.1 -?/. - c.1286C>T r.(?) p.(Pro429Leu)


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