Variant #0000618962 (NC_000023.10:g.120094502G>C, NM_001080142.1:c.*2550C>G (CT47A5))

Chromosome X
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.120094502G>C
DNA change (hg38) g.120960648G>C
Published as CT47A6(NM_001080141.1):c.581C>G (p.S194W)
ISCN -
DB-ID CT47A5_000001
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) Retrieve
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 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CT47A7 NM_001080140.1 ?/. - c.-4303C>G r.(?) p.(=)
CT47A6 NM_001080141.1 ?/. - c.581C>G r.(?) p.(Ser194Trp)
CT47A5 NM_001080142.1 ?/. - c.*2550C>G r.(=) p.(=)


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