Variant #0000611486 (NC_000008.10:g.144803222G>A, NM_198488.3:c.*4869C>T (FAM83H))

Chromosome 8
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.144803222G>A
DNA change (hg38) g.143721052G>A
Published as MAPK15(NM_139021.3):c.970G>A (p.A324T)
ISCN -
DB-ID FAM83H_000015
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.970G>A r.(?) p.(Ala324Thr)
FAM83H NM_198488.3 -?/. - c.*4869C>T r.(=) p.(=)


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