Variant #0000976635 (NC_000005.9:g.14690188A>G, NM_138348.4:c.635A>G (FAM105B))

Chromosome 5
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.14690188A>G
DNA change (hg38) -
Published as OTULIN(NM_138348.5):c.635A>G (p.Q212R), OTULIN(NM_138348.6):c.635A>G (p.Q212R)
ISCN -
DB-ID FAM105B_000003 See all 3 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) 0.00012 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FAM105B NM_138348.4 ?/. - c.635A>G r.(?) p.(Gln212Arg)


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