Variant #0001052748 (NC_000007.13:g.99051650C>T, NM_015545.3:c.-15362G>A (PTCD1))

Chromosome 7
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.99051650C>T
DNA change (hg38) -
Published as CPSF4(NM_006693.4):c.632C>T (p.(Ser211Phe))
ISCN -
DB-ID ATP5J2_000003
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 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CPSF4 NM_001081559.1 -?/. - c.571-14C>T r.(=) p.(=)
ATP5J2-PTCD1 NM_001198879.1 -?/. - c.121+6059G>A r.(=) p.(=)
BUD31 NM_003910.3 -?/. - c.*34586C>T r.(=) p.(=)
ATP5J2 NM_004889.3 -?/. - c.*4300G>A r.(=) p.(=)
PTCD1 NM_015545.3 -?/. - c.-15362G>A r.(?) p.(=)


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