Variant #0000727479 (NC_000019.9:g.50189487C>T, NM_152359.2:c.-5125C>T (CPT1C))

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.50189487C>T
DNA change (hg38) -
Published as PRMT1(NM_001536.5):c.897C>T (p.T299=)
ISCN -
DB-ID CPT1C_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) 0.00013 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 2021-02-08 18:36:18 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ADM5 NM_001101340.1 -?/. - c.-3608C>T r.(?) p.(=)
PRMT1 NM_001207042.2 -?/. - c.639C>T r.(?) p.(Thr213=)
CPT1C NM_152359.2 -?/. - c.-5125C>T r.(?) p.(=)


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