Variant #0000274610 (NC_000007.13:g.117375432G>T, NM_033427.2:c.3579C>A (CTTNBP2))

Chromosome 7
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.117375432G>T
DNA change (hg38) g.117735378G>T
Published as CTTNBP2(NM_033427.2):c.3579C>A (p.I1193=), CTTNBP2(NM_033427.3):c.3579C>A (p.(Ile1193=))
ISCN -
DB-ID CTTNBP2_000001 See all 2 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) 0.00185 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 2024-04-19 20:27:30 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CTTNBP2 NM_033427.2 -/. - c.3579C>A r.(?) p.(Ile1193=)


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