Variant #0000309413 (NC_000009.11:g.35685460C>T, NM_003289.3:c.463G>A (TPM2))

Chromosome 9
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.35685460C>T
DNA change (hg38) g.35685463C>T
Published as TPM2(NM_001301227.2):c.463G>A (p.A155T)
ISCN -
DB-ID TPM2_000053 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) Retrieve
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CA9 NM_001216.2 +?/. - c.*4438C>T r.(=) p.(=)
TPM2 NM_003289.3 +?/. - c.463G>A r.(?) p.(Ala155Thr)
TPM2 NM_213674.1 +?/. - c.463G>A r.(?) p.(Ala155Thr)


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