Variant #0001005032 (NC_000019.9:g.507765C>T, NM_130760.2:c.*2800C>T (MADCAM1))

Chromosome 19
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.507765C>T
DNA change (hg38) -
Published as TPGS1(NM_033513.2):c.259C>T (p.(Pro87Ser))
ISCN -
DB-ID MADCAM1_000006
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) 0.00068 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     
TPGS1 NM_033513.2 -?/. - c.259C>T r.(?) p.(Pro87Ser)
MADCAM1 NM_130760.2 -?/. - c.*2800C>T r.(=) p.(=)


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