Variant #0000656351 (NC_000009.11:g.35685747G>A, NM_003289.3:c.271C>T (TPM2))

Chromosome 9
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.35685747G>A
DNA change (hg38) g.35685750G>A
Published as TPM2(NM_001301227.1):c.271C>T (p.R91C)
ISCN -
DB-ID CA9_000020
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-03-23 16:13:27 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CA9 NM_001216.2 ?/. - c.*4725G>A r.(=) p.(=)
TPM2 NM_003289.3 ?/. - c.271C>T r.(?) p.(Arg91Cys)
TPM2 NM_213674.1 ?/. - c.271C>T r.(?) p.(Arg91Cys)


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