Variant #0000301501 (NC_000016.9:g.53720436C>T, NM_015272.2:c.685G>A (RPGRIP1L))

Chromosome 16
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.53720436C>T
DNA change (hg38) g.53686524C>T
Published as RPGRIP1L(NM_015272.4):c.685G>A (p.A229T), RPGRIP1L(NM_015272.5):c.685G>A (p.A229T, p.(Ala229Thr))
ISCN -
DB-ID RPGRIP1L_000053 See all 8 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) 0.03552 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RPGRIP1L NM_015272.2 -?/. - c.685G>A r.(?) p.(Ala229Thr)


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