Variant #0001037513 (NC_000009.11:g.35683248_35683249insCG, NC_000009.11(NM_003289.3):c.773-10_773-9insGC (TPM2))

Chromosome 9
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.35683248_35683249insCG
DNA change (hg38) -
Published as TPM2(NM_003289.4):c.773-10_773-9insGC
ISCN -
DB-ID CA9_000034
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 2025-05-05 21:14:00 +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     
CA9 NM_001216.2 -?/. - c.*2226_*2227insCG r.(=) p.(=)
TPM2 NM_003289.3 -?/. - c.773-10_773-9insGC r.(=) p.(=)
TPM2 NM_213674.1 -?/. - c.772+995_772+996insGC r.(=) p.(=)


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