Variant #0000800962 (NC_000003.11:g.129155670C>T, NM_052985.2:c.-3504C>T (IFT122))

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.129155670C>T
DNA change (hg38) -
Published as MBD4(NM_003925.3):c.817G>A (p.A273T)
ISCN -
DB-ID MBD4_000004
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) 0.08014 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MBD4 NM_003925.1 -/. - c.817G>A r.(?) p.(Ala273Thr)
IFT122 NM_052985.2 -/. - c.-3504C>T r.(?) p.(=)


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