Variant #0000996854 (NC_000008.10:g.10480680G>A, NM_178857.5:c.32C>T (RP1L1))

Chromosome 8
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.10480680G>A
DNA change (hg38) -
Published as RP1L1(NM_178857.5):c.32C>T (p.(Pro11Leu)), RP1L1(NM_178857.6):c.32C>T (p.P11L)
ISCN -
DB-ID RP1L1_000291 See all 5 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) 0.00077 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 2024-08-28 13:16:32 +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     
RP1L1 NM_178857.5 -?/. - c.32C>T r.(?) p.(Pro11Leu)


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