Variant #0000995242 (NC_000006.11:g.109763831G>C, NM_014797.2:c.*23223C>G (ZBTB24))

Chromosome 6
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.109763831G>C
DNA change (hg38) -
Published as SMPD2(NM_003080.2):c.491+3G>C (p.?)
ISCN -
DB-ID MICAL1_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) 0.00251 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +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     
PPIL6 NM_001111298.2 -?/. - c.-2038C>G r.(?) p.(=)
SMPD2 NM_003080.2 -?/. - c.491+3G>C r.spl? p.?
ZBTB24 NM_014797.2 -?/. - c.*23223C>G r.(=) p.(=)
MICAL1 NM_022765.3 -?/. - c.*1563C>G r.(=) p.(=)


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