Variant #0000254825 (NC_000003.11:g.160137252A>G, NM_020800.2:c.-20365T>C (IFT80))

Chromosome 3
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.160137252A>G
DNA change (hg38) g.160419464A>G
Published as SMC4(NM_001002800.2):c.1778A>G (p.N593S)
ISCN -
DB-ID SMC4_000001
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) 1.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SMC4 NM_001002800.1 -?/. - c.1778A>G r.(?) p.(Asn593Ser)
IFT80 NM_020800.2 -?/. - c.-20365T>C r.(?) p.(=)


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