Variant #0000949281 (NC_000009.11:g.35683241_35683242insT, NC_000009.11(NM_003289.3):c.773-4_773-3insA (TPM2))

Chromosome 9
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.35683241_35683242insT
DNA change (hg38) -
Published as TPM2(NM_001301227.1):c.773-4_773-3insA, TPM2(NM_001301227.2):c.773-4_773-3insA
ISCN -
DB-ID CA9_000013 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) 0.00434 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2023-11-27 17:35:39 +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.*2219_*2220insT r.(=) p.(=)
TPM2 NM_003289.3 -/. - c.773-4_773-3insA r.spl? p.?
TPM2 NM_213674.1 -/. - c.772+1001_772+1002insA r.(=) p.(=)


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