Variant #0001039517 (NC_000012.11:g.9085593_9085604del, NM_001207024.1:c.*8813_*8824del (M6PR))

Chromosome 12
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.9085593_9085604del
DNA change (hg38) -
Published as PHC1(NM_004426.2):c.1540_1551delAAGATGTCAGCT (p.K514_A517del), PHC1(NM_004426.3):c.1540_1551del (p.(Lys514_Ala517del))
ISCN -
DB-ID M6PR_000006 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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
M6PR NM_001207024.1 ?/. - c.*8813_*8824del r.(=) p.(=)
PHC1 NM_004426.2 ?/. - c.1540_1551del r.(?) p.(Lys514_Ala517del)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.