Variant #0000851783 (NC_000008.10:g.116599406C>T, NM_014112.2:c.2522G>A (TRPS1))

Chromosome 8
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.116599406C>T
DNA change (hg38) -
Published as TRPS1(NM_014112.4):c.2522G>A (p.R841K), TRPS1(NM_014112.5):c.2522G>A (p.(Arg841Lys))
ISCN -
DB-ID TRPS1_000046 See all 2 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) 1.0E-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 2022-05-09 15:40:45 +02:00 (CEST)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TRPS1 NM_014112.2 ?/. - c.2522G>A r.(?) p.(Arg841Lys)


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