Variant #0000320104 (NC_000006.11:g.109787476C>T, NM_014797.2:c.1672G>A (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.109787476C>T
DNA change (hg38) g.109466273C>T
Published as ZBTB24(NM_014797.2):c.1672G>A (p.D558N, p.(Asp558Asn))
ISCN -
DB-ID ZBTB24_000015 See all 3 reported entries
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) 0.00261 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2019-12-04 15:24:38 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ZBTB24 NM_014797.2 -?/. - c.1672G>A r.(?) p.(Asp558Asn)
MICAL1 NM_022765.3 -?/. - c.-10598G>A r.(?) p.(=)


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