Variant #0000994662 (NC_000005.9:g.134366994C>A, NM_002653.4:c.374G>T (PITX1))

Chromosome 5
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.134366994C>A
DNA change (hg38) -
Published as PITX1(NM_002653.4):c.374G>T (p.(Trp125Leu))
ISCN -
DB-ID H2AFY_000011
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) 0 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PITX1 NM_002653.4 ?/. - c.374G>T r.(?) p.(Trp125Leu)
H2AFY NM_004893.2 ?/. - c.*303672G>T r.(=) p.(=)


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