Variant #0000539525 (NC_000010.10:g.13320306_13320308dup, NM_006214.3:c.1010_1012dup (PHYH))

Chromosome 10
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.13320306_13320308dup
DNA change (hg38) g.13278306_13278308dup
Published as PHYH(NM_001037537.1):c.710_712dupATC (p.N237_L238insH), PHYH(NM_001037537.2):c.710_712dupATC (p.N237_L238insH), PHYH(NM_006214.4):c.1010_1012dupATC...
ISCN -
DB-ID PHYH_000023 See all 4 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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PHYH NM_006214.3 -?/. - c.1010_1012dup r.(?) p.(Asn337_Leu338insHis)


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