Variant #0000555021 (NC_000015.9:g.63335910G>A, NC_000015.9(NM_001018005.1):c.115-316G>A (TPM1))

Chromosome 15
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.63335910G>A
DNA change (hg38) g.63043711G>A
Published as TPM1(NM_001018007.2):c.120G>A (p.E40=), TPM1(NM_001018020.1):c.120G>A (p.E40=)
ISCN -
DB-ID TPM1_000052 See all 4 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) 0.0002 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TPM1 NM_001018005.1 -/. - c.115-316G>A r.(=) p.(=)


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