Variant #0000996221 (NC_000007.13:g.131241049_131241054dup, NM_001018111.2:c.84_89dup (PODXL))

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.131241049_131241054dup
DNA change (hg38) -
Published as PODXL(NM_001018111.2):c.72_77dupGTCGCC (p.(Pro26_Ser27insSerPro)), PODXL(NM_001018111.2):c.84_89dupGTCGCC (p.P30_S31dup), PODXL(NM_005397.4):c.84_8...
ISCN -
DB-ID PODXL_000007 See all 3 reported entries
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     
PODXL NM_001018111.2 -?/. - c.84_89dup r.(?) p.(Pro30_Ser31dup)


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