Variant #0001002483 (NC_000016.9:g.67680807T>G, NM_022914.2:c.*10702A>C (ACD))

Chromosome 16
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.67680807T>G
DNA change (hg38) -
Published as RLTPR(NM_001013838.1):c.542T>G (p.(Val181Gly))
ISCN -
DB-ID ACD_000069
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 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RLTPR NM_001013838.1 ?/. - c.542T>G r.(?) p.(Val181Gly)
ACD NM_022914.2 ?/. - c.*10702A>C r.(=) p.(=)


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