Variant #0000544654 (NC_000011.9:g.58919380T>C, NM_001312909.1:c.239T>C (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.58919380T>C
DNA change (hg38) g.59151907T>C
Published as FAM111A(NM_001142519.1):c.239T>C (p.(Val80Ala))
ISCN -
DB-ID FAM111A_000002
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-11-27 17:27:23 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FAM111A NM_001312909.1 -?/. - c.239T>C r.(?) p.(Val80Ala)
FAM111A NM_022074.3 -?/. - c.239T>C r.(?) p.(Val80Ala)


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