Variant #0001003710 (NC_000017.10:g.7495635_7495636del, NM_004870.3:c.*4766_*4767del (MPDU1))

Chromosome 17
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.7495635_7495636del
DNA change (hg38) -
Published as FXR2(NM_004860.3):c.1864_1865delAG (p.(Ser622fs))
ISCN -
DB-ID MPDU1_000018
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 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     
FXR2 NM_004860.3 +?/. - c.1864_1865del r.(?) p.(Ser622Profs*10)
MPDU1 NM_004870.3 +?/. - c.*4766_*4767del r.(=) p.(=)
SOX15 NM_006942.1 +?/. - c.-2640_-2639del r.(?) p.(=)


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