Variant #0000322839 (NC_000012.11:g.49722763G>T, NM_006262.3:c.*30627G>T (PRPH))

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.49722763G>T
DNA change (hg38) g.49328980G>T
Published as TROAP(NM_001100620.1):c.*4728G>T (p.(=))
ISCN -
DB-ID C1QL4_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) 0.00026 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     
C1QL4 NM_001008223.1 ?/. - c.*4074C>A r.(=) p.(=)
TROAP NM_005480.3 ?/. - c.945G>T r.(?) p.(Leu315Phe)
PRPH NM_006262.3 ?/. - c.*30627G>T r.(=) p.(=)


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