Variant #0000566346 (NC_000019.9:g.1487610C>T, NM_138393.1:c.-3659C>T (REEP6))

Chromosome 19
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.1487610C>T
DNA change (hg38) g.1487611C>T
Published as PCSK4(NM_017573.4):c.674G>A (p.R225Q)
ISCN -
DB-ID PCSK4_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) 6.0E-5 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 2019-07-18 18:22:55 +02:00 (CEST)
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)     

RNA change     

Protein     
PCSK4 NM_017573.3 -?/. - c.674G>A r.(?) p.(Arg225Gln)
REEP6 NM_138393.1 -?/. - c.-3659C>T r.(?) p.(=)


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