Variant #0000803759 (NC_000008.10:g.94740472G>C, NM_145269.3:c.817G>C (FAM92A1))

Chromosome 8
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.94740472G>C
DNA change (hg38) -
Published as FAM92A(NM_145269.4):c.817G>C (p.D273H)
ISCN -
DB-ID FAM92A1_000001
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) 2.0E-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 2021-09-17 14:40:49 +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     
FAM92A1 NM_145269.3 ?/. - c.817G>C r.(?) p.(Asp273His)
RBM12B NM_203390.2 ?/. - c.*5161C>G r.(=) p.(=)


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