Variant #0000612368 (NC_000010.10:g.13320306_13320308dup, NM_006214.3:c.1010_1012dup (PHYH))

Chromosome 10
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.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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
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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)


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