Variant #0001002204 (NC_000016.9:g.3021644C>T, NM_172229.2:c.*3623C>T (KREMEN2))

Chromosome 16
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.3021644C>T
DNA change (hg38) -
Published as PAQR4(NM_152341.3):c.517C>T (p.(Arg173Trp))
ISCN -
DB-ID KREMEN2_000008
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PKMYT1 NM_004203.4 ?/. - c.*1310G>A r.(=) p.(=)
PAQR4 NM_152341.3 ?/. - c.517C>T r.(?) p.(Arg173Trp)
KREMEN2 NM_172229.2 ?/. - c.*3623C>T r.(=) p.(=)


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