Variant #0000805786 (NC_000012.11:g.49729891C>T, NM_005480.3:c.*4491C>T (TROAP))

Chromosome 12
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.49729891C>T
DNA change (hg38) -
Published as C1QL4(NM_001008223.2):c.370G>A (p.E124K)
ISCN -
DB-ID C1QL4_000006
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) 1.0E-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 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C1QL4 NM_001008223.1 ?/. - c.370G>A r.(?) p.(Glu124Lys)
TROAP NM_005480.3 ?/. - c.*4491C>T r.(=) p.(=)


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