Variant #0000966447 (NC_000011.9:g.58920252A>T, NM_001312909.1:c.1111A>T (FAM111A))

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.58920252A>T
DNA change (hg38) -
Published as FAM111A(NM_001142519.1):c.1111A>T (p.(Thr371Ser)), FAM111A(NM_022074.4):c.1111A>T (p.T371S)
ISCN -
DB-ID FAM111A_000009 See all 2 reported entries
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) 0.00019 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 2024-02-26 20:06:56 +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.1111A>T r.(?) p.(Thr371Ser)
FAM111A NM_022074.3 ?/. - c.1111A>T r.(?) p.(Thr371Ser)


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