Variant #0000524222 (NC_000005.9:g.134367205T>C, NC_000005.9(NM_002653.4):c.170-7A>G (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.134367205T>C
DNA change (hg38) g.135031515T>C
Published as PITX1(NM_002653.4):c.170-7A>G (p.(=))
ISCN -
DB-ID H2AFY_000001
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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     
PITX1 NM_002653.4 ?/. - c.170-7A>G r.(=) p.(=)
H2AFY NM_004893.2 ?/. - c.*303461A>G r.(=) p.(=)


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