Variant #0000975562 (NC_000003.11:g.129156534G>A, NM_052985.2:c.-2640G>A (IFT122))

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.129156534G>A
DNA change (hg38) -
Published as MBD4(NM_003925.3):c.335+29C>T
ISCN -
DB-ID MBD4_000010
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) 4.0E-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 2024-04-19 20:27:30 +02:00 (CEST)
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.335+29C>T r.(=) p.(=)
IFT122 NM_052985.2 -?/. - c.-2640G>A r.(?) p.(=)


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