Variant #0000316943 (NC_000015.9:g.63336295G>C, NM_001018005.1:c.184G>C (TPM1))

Chromosome 15
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.63336295G>C
DNA change (hg38) g.63044096G>C
Published as TPM1(NM_001018004.2):c.184G>C (p.E62Q), TPM1(NM_001365776.1):c.184G>C (p.E62Q)
ISCN -
DB-ID TPM1_000004 See all 5 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) 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-08-28 13:16:32 +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.184G>C r.(?) p.(Glu62Gln)


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