Variant #0000848324 (NC_000001.10:g.155264936C>T, NM_000298.5:c.665G>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.155264936C>T
DNA change (hg38) -
Published as PKLR(NM_000298.6):c.665G>A (p.G222E)
ISCN -
DB-ID PKLR_000346 See all 3 reported entries
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 2022-05-09 15:40:45 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
PKLR NM_000298.5 ?/. - c.665G>A - r.(?) p.(Gly222Glu)
HCN3 NM_020897.2 ?/. - c.*6682C>T - r.(=) p.(=)


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