Variant #0000321532 (NC_000010.10:g.51225877G>A, NC_000010.10(NM_003631.2):c.1456-95162C>T (PARG))

Chromosome 10
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.51225877G>A
DNA change (hg38) -
Published as AGAP8(NM_001077686.2):c.1105C>T (p.(Pro369Ser))
ISCN -
DB-ID AGAP8_000002
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) 0.04706 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AGAP8 NM_001077686.1 ?/. - c.1105C>T r.(?) p.(Pro369Ser)
PARG NM_003631.2 ?/. - c.1456-95162C>T r.(=) p.(=)


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