Variant #0000716725 (NC_000001.10:g.120263925_120263928del, NM_006623.3:c.271_274del (PHGDH))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.120263925_120263928del
DNA change (hg38) -
Published as PHGDH(NM_006623.3):c.271_274delAAGG (p.K91Afs*5), PHGDH(NM_006623.4):c.271_274delAAGG (p.K91Afs*5)
ISCN -
DB-ID PHGDH_000023 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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2024-10-29 20:49:11 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PHGDH NM_006623.3 +?/. - c.271_274del r.(?) p.(Lys91Alafs*5)


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