Variant #0000841433 (NC_000008.10:g.116426675T>C, NM_014112.2:c.3461A>G (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.116426675T>C
DNA change (hg38) -
Published as -
ISCN -
DB-ID TRPS1_000044
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs756910279
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-5 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2022-02-27 17:22:01 +01:00 (CET)
Date last edited 2022-09-26 12:22:42 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TRPS1 NM_014112.2 ?/. - c.3461A>G r.(?) p.(Tyr1154Cys)


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