Variant #0000611487 (NC_000008.10:g.144808491A>T, NM_198488.3:c.3140T>A (FAM83H))

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.144808491A>T
DNA change (hg38) g.143726321A>T
Published as FAM83H(NM_198488.5):c.3140T>A (p.I1047N)
ISCN -
DB-ID FAM83H_000016
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) Retrieve
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2019-12-04 15:24:38 +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     
MAPK15 NM_139021.2 ?/. - c.*4070A>T r.(=) p.(=)
FAM83H NM_198488.3 ?/. - c.3140T>A r.(?) p.(Ile1047Asn)


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