Variant #0000611490 (NC_000008.10:g.144809500T>C, NM_198488.3:c.2131A>G (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.144809500T>C
DNA change (hg38) g.143727330T>C
Published as FAM83H(NM_198488.3):c.2131A>G (p.K711E)
ISCN -
DB-ID FAM83H_000019
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) 1.0E-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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +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.*5079T>C r.(=) p.(=)
FAM83H NM_198488.3 ?/. - c.2131A>G r.(?) p.(Lys711Glu)


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