Variant #0000533421 (NC_000008.10:g.10468353G>C, NM_178857.5:c.3255C>G (RP1L1))

Chromosome 8
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.10468353G>C
DNA change (hg38) g.10610843G>C
Published as RP1L1(NM_178857.5):c.3255C>G (p.I1085M), RP1L1(NM_178857.6):c.3255C>G (p.I1085M)
ISCN -
DB-ID RP1L1_000081 See all 6 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) 0.00213 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RP1L1 NM_178857.5 -/. - c.3255C>G r.(?) p.(Ile1085Met)


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