Variant #0000798856 (NC_000001.10:g.15772212C>T, NM_007272.2:c.760C>T (CTRC))

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.15772212C>T
DNA change (hg38) -
Published as CTRC(NM_007272.2):c.760C>T (p.R254W), CTRC(NM_007272.3):c.760C>T (p.R254W)
ISCN -
DB-ID CTRC_000005 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) 0.00453 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 2021-09-17 14:40:49 +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     
CTRC NM_007272.2 ?/. - c.760C>T r.(?) p.(Arg254Trp)


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