Variant #0000993269 (NC_000003.11:g.129155784C>T, NM_052985.2:c.-3390C>T (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.129155784C>T
DNA change (hg38) -
Published as MBD4(NM_003925.3):c.703G>A (p.V235M)
ISCN -
DB-ID MBD4_000012
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 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MBD4 NM_003925.1 ?/. - c.703G>A r.(?) p.(Val235Met)
IFT122 NM_052985.2 ?/. - c.-3390C>T r.(?) p.(=)


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