Variant #0000538952 (NC_000010.10:g.103990530C>T, NM_005029.3:c.650G>A (PITX3))

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.103990530C>T
DNA change (hg38) g.102230773C>T
Published as PITX3(NM_005029.3):c.650G>A (p.G217D)
ISCN -
DB-ID PITX3_000022
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-11-14 15:36:30 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PITX3 NM_005029.3 ?/. - c.650G>A r.(?) p.(Gly217Asp)
ELOVL3 NM_152310.1 ?/. - c.*1521C>T r.(=) p.(=)


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