Variant #0001024720 (NC_000003.11:g.129155659T>G, NM_052985.2:c.-3515T>G (IFT122))

Chromosome 3
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.129155659T>G
DNA change (hg38) -
Published as MBD4(NM_003925.3):c.828A>C (p.E276D)
ISCN -
DB-ID MBD4_000013
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) 9.0E-5 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2025-02-07 18:57:27 +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     
MBD4 NM_003925.1 ?/. - c.828A>C r.(?) p.(Glu276Asp)
IFT122 NM_052985.2 ?/. - c.-3515T>G r.(?) p.(=)


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