Variant #0000604847 (NC_000001.10:g.155247568C>T, NM_000298.5:c.*12795G>A (PKLR))

Chromosome 1
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.155247568C>T
DNA change (hg38) g.155277777C>T
Published as -
ISCN -
DB-ID CLK2_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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-12-04 14:54:23 +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)     

Haplotype     

RNA change     

Protein     
PKLR NM_000298.5 ?/. - c.*12795G>A - r.(=) p.(=)
CLK2 NM_003993.2 ?/. - c.-4577G>A - r.(?) p.(=)
HCN3 NM_020897.2 ?/. - c.187C>T - r.(?) p.(Arg63Trp)


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