Variant #0000883496 (NC_000001.10:g.53676371T>C, NM_000098.2:c.1025T>C (CPT2))

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.53676371T>C
DNA change (hg38) -
Published as CPT2(NM_000098.3):c.1025T>C (p.(Met342Thr), p.M342T)
ISCN -
DB-ID CPT2_000052 See all 2 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) 0.00106 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2022-11-01 13:01:21 +01:00 (CET)
Date last edited 2024-04-19 20:20:39 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CPT2 NM_000098.2 ?/. - c.1025T>C r.(?) p.(Met342Thr)
C1orf123 NM_017887.1 ?/. - c.*3960A>G r.(=) p.(=)


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