Variant #0000962540 (NC_000003.11:g.160142830_160142841dup, NM_020800.2:c.-25935_-25924dup (IFT80))

Chromosome 3
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.160142830_160142841dup
DNA change (hg38) -
Published as SMC4(NM_001002800.3):c.2478+18_2478+29dupTGTGTGTGTGTG
ISCN -
DB-ID IFT80_000047
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2024-02-26 20:06:56 +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     
SMC4 NM_001002800.1 -/. - c.2478+23_2478+34dup r.(=) p.(=)
IFT80 NM_020800.2 -/. - c.-25935_-25924dup r.(?) p.(=)


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