Variant #0000316942 (NC_000015.9:g.63336291C>T, NM_001018005.1:c.180C>T (TPM1))

Chromosome 15
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.63336291C>T
DNA change (hg38) g.63044092C>T
Published as TPM1(NM_001018004.2):c.180C>T (p.Y60=), TPM1(NM_001018005.1):c.180C>T (p.Y60=), TPM1(NM_001365776.1):c.180C>T (p.Y60=)
ISCN -
DB-ID TPM1_000093 See all 4 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) 0.00064 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2025-02-07 18:57:27 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TPM1 NM_001018005.1 -?/. - c.180C>T r.(?) p.(Tyr60=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.