Variant #0000621098 (NC_000002.11:g.62066572G>A, NM_001201543.1:c.1567C>T (FAM161A))

Chromosome 2
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.62066572G>A
DNA change (hg38) g.61839437G>A
Published as FAM161A(NM_001201543.1):c.1567C>T (p.R523*), FAM161A(NM_001201543.2):c.1567C>T (p.R523*)
ISCN -
DB-ID FAM161A_000016 See all 20 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) 5.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-06 12:43:26 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FAM161A NM_001201543.1 +/. - c.1567C>T r.(?) p.(Arg523Ter)


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