Variant #0000980894 (NC_000014.8:g.36192311del, NM_194301.2:c.2027del (RALGAPA1))

Chromosome 14
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.36192311del
DNA change (hg38) -
Published as RALGAPA1(NM_001346249.2):c.2027del (p.(Asn676IlefsTer15))
ISCN -
DB-ID RALGAPA1_000018
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 2024-04-19 20:27:30 +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     
RALGAPA1 NM_014990.1 +?/. - c.2027del r.(?) p.(Asn676Ilefs*15)
RALGAPA1 NM_194301.2 +?/. - c.2027del r.(?) p.(Asn676Ilefs*15)


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