Variant #0000524264 (NC_000005.9:g.137347497C>T, NM_016603.2:c.508G>A (FAM13B))

Chromosome 5
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.137347497C>T
DNA change (hg38) g.138011808C>T
Published as FAM13B(NM_016603.3):c.508G>A (p.A170T)
ISCN -
DB-ID FAM13B_000004
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PKD2L2 NM_001300921.1 ?/. - c.*69442C>T r.(=) p.(=)
FAM13B NM_016603.2 ?/. - c.508G>A r.(?) p.(Ala170Thr)


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