Variant #0000333744 (NC_000023.10:g.38145423_38145443dup, NM_001034853.1:c.2820_2840dup (RPGR))

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.38145423_38145443dup
DNA change (hg38) g.38286170_38286190dup
Published as RPGR(NM_001034853.1):c.2840_2841insAGGGGAGGATGGAGAAGGGGA (p.(Gly941_Glu947dup)), RPGR(NM_001034853.2):c.2820_2840dupAGGGGAGGATGGAGAAGGGGA (p.D943_...)
ISCN -
DB-ID RPGR_000034 See all 4 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) Retrieve
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 2022-05-09 15:51:19 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RPGR NM_000328.2 ?/. - c.1905+915_1905+935dup r.(=) p.(=)
RPGR NM_001034853.1 ?/. - c.2820_2840dup r.(?) p.(Asp943_Glu949dup)


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