Variant #0000528062 (NC_000006.11:g.17601124_17601154del, NM_016255.2:c.484_514del (FAM8A1))

Chromosome 6
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.17601124_17601154del
DNA change (hg38) g.17600893_17600923del
Published as FAM8A1(NM_016255.2):c.484_514del (p.(Ala162ThrfsTer7))
ISCN -
DB-ID FAM8A1_000002
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-18 14:46:08 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FAM8A1 NM_016255.2 -?/. - c.484_514del r.(?) p.(Ala162ThrfsTer7)


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