Variant #0000623277 (NC_000015.9:g.63335110G>A, NM_001018005.1:c.82G>A (TPM1))

Chromosome 15
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.63335110G>A
DNA change (hg38) g.63042911G>A
Published as TPM1(NM_001018004.1):c.82G>A (p.D28N), TPM1(NM_001018004.2):c.82G>A (p.D28N)
ISCN -
DB-ID TPM1_000120 See all 3 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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-12-06 12:43:26 +01:00 (CET)
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.82G>A r.(?) p.(Asp28Asn)


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