Variant #0000930255 (NC_000013.10:g.48986411T>C, NC_000013.10(NM_000321.2):c.1695+30832T>C (RB1))

Chromosome 13
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.48986411T>C
DNA change (hg38) -
Published as LPAR6(NM_005767.7):c.149A>G (p.N50S)
ISCN -
DB-ID LPAR6_000026
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) 2.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-07-07 10:10:56 +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     
RB1 NM_000321.2 ?/. - c.1695+30832T>C r.(=) p.(=)
LPAR6 NM_005767.5 ?/. - c.149A>G r.(?) p.(Asn50Ser)


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