Variant #0000573671 (NC_000023.10:g.134948078C>T, NM_001007551.3:c.247G>A (CT45A5))

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.134948078C>T
DNA change (hg38) g.135831368C>T
Published as CT45A5(NM_001007551.3):c.247G>A (p.(Gly83Arg))
ISCN -
DB-ID CT45A5_000018 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) 0.01646 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CT45A5 NM_001007551.3 -?/. - c.247G>A r.(?) p.(Gly83Arg)
CT45A6 NM_001017438.1 -?/. - c.*15330G>A r.(=) p.(=)


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