Variant #0000980895 (NC_000014.8:g.36197612A>C, NM_194301.2:c.1692T>G (RALGAPA1))

Chromosome 14
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.36197612A>C
DNA change (hg38) -
Published as RALGAPA1(NM_001346249.2):c.1692T>G (p.(Ile564Met))
ISCN -
DB-ID RALGAPA1_000019
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 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 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RALGAPA1 NM_014990.1 ?/. - c.1692T>G r.(?) p.(Ile564Met)
RALGAPA1 NM_194301.2 ?/. - c.1692T>G r.(?) p.(Ile564Met)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.