Variant #0000305745 (NC_000005.9:g.137241887T>C, NM_016603.2:c.*34027A>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.137241887T>C
DNA change (hg38) g.137906198T>C
Published as PKD2L2(NM_001258449.1):c.747-8T>C
ISCN -
DB-ID PKD2L2_000001
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) 0.00019 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 2018-01-15 20:58:59 +01:00 (CET)
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.747-8T>C r.(=) p.(=)
PKD2L2 NM_014386.2 -?/. - c.747-8T>C r.(=) p.(=)
FAM13B NM_016603.2 -?/. - c.*34027A>G r.(=) p.(=)


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