Variant #0000619956 (NC_000023.10:g.89177276C>A, NM_138960.3:c.192C>A (TGIF2LX))

Chromosome X
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.89177276C>A
DNA change (hg38) g.89922277C>A
Published as TGIF2LX(NM_138960.3):c.192C>A (p.I64=), TGIF2LX(NM_138960.4):c.192C>A (p.(Ile64=))
ISCN -
DB-ID TGIF2LX_000011 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) 4.0E-5 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 2019-12-04 15:24:38 +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     
TGIF2LX NM_138960.3 -?/. - c.192C>A r.(?) p.(Ile64=)


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