Variant #0000335374 (NC_000023.10:g.120009295T>C, NM_001242922.1:c.*2221A>G (CT47A12))

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.120009295T>C
DNA change (hg38) g.120875441T>C
Published as CT47B1(NM_001145718.1):c.230A>G (p.(Gln77Arg))
ISCN -
DB-ID CT47B1_000004
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) 0.00138 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 2018-01-15 20:58:59 +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     
CT47B1 NM_001145718.1 ?/. - c.230A>G r.(?) p.(Gln77Arg)
CT47A12 NM_001242922.1 ?/. - c.*2221A>G r.(=) p.(=)


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