Variant #0000809619 (NC_000022.10:g.37492065del, NM_153609.2:c.497del (TMPRSS6))

Chromosome 22
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.37492065del
DNA change (hg38) -
Published as TMPRSS6(NM_001374504.1):c.470del (p.(Leu157Argfs*37)), TMPRSS6(NM_153609.3):c.497delT (p.L166Rfs*37)
ISCN -
DB-ID TMPRSS6_000051 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) 2.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TMPRSS6 NM_153609.2 +/. - c.497del r.(?) p.(Leu166ArgfsTer37)


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