Variant #0000805202 (NC_000011.9:g.58919451T>A, NM_001312909.1:c.310T>A (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.58919451T>A
DNA change (hg38) -
Published as FAM111A(NM_001142519.1):c.310T>A (p.(Leu104Ile))
ISCN -
DB-ID FAM111A_000012
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) 0.00232 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2021-09-17 14:40:49 +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.310T>A r.(?) p.(Leu104Ile)
FAM111A NM_022074.3 -?/. - c.310T>A r.(?) p.(Leu104Ile)


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