Variant #0000271408 (NC_000008.10:g.144809804G>A, NM_198488.3:c.1827C>T (FAM83H))

Chromosome 8
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.144809804G>A
DNA change (hg38) g.143727634G>A
Published as FAM83H(NM_198488.3):c.1827C>T (p.Y609=), FAM83H(NM_198488.5):c.1827C>T (p.Y609=)
ISCN -
DB-ID FAM83H_000005 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) 0.94486 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +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     
FAM83H NM_198488.3 -/. - c.1827C>T r.(?) p.(Tyr609=)


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