Variant #0000524263 (NC_000005.9:g.137278733A>C, NC_000005.9(NM_016603.2):c.2359-6T>G (FAM13B))

Chromosome 5
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.137278733A>C
DNA change (hg38) g.137943044A>C
Published as FAM13B(NM_001101800.1):c.2275-6T>G (p.(=))
ISCN -
DB-ID FAM13B_000003
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) 0.00605 View details
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 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.*678A>C r.(=) p.(=)
PKD2L2 NM_014386.2 -?/. - c.*2897A>C r.(=) p.(=)
FAM13B NM_016603.2 -?/. - c.2359-6T>G r.(=) p.(=)


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