Variant #0001053247 (NC_000009.11:g.35685065T>C, NC_000009.11(NM_003289.3):c.563+201A>G (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.35685065T>C
DNA change (hg38) -
Published as TPM2(NM_001301227.2):c.635A>G (p.(Glu212Gly))
ISCN -
DB-ID CA9_000036
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CA9 NM_001216.2 ?/. - c.*4043T>C r.(=) p.(=)
TPM2 NM_003289.3 ?/. - c.563+201A>G r.(=) p.(=)
TPM2 NM_213674.1 ?/. - c.635A>G r.(?) p.(Glu212Gly)


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