Variant #0000319188 (NC_000009.11:g.12694136_12694137del, NM_000550.2:c.140_141del (TYRP1))

Chromosome 9
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.12694136_12694137del
DNA change (hg38) g.12694136_12694137del
Published as TYRP1(NM_000550.2):c.140_141delCT (p.P47Rfs*19), TYRP1(NM_000550.3):c.140_141delCT (p.P47Rfs*19)
ISCN -
DB-ID TYRP1_000036 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) 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2025-02-07 18:57:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TYRP1 NM_000550.2 +/. - c.140_141del r.(?) p.(Pro47ArgfsTer19)


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