Variant #0000328616 (NC_000020.10:g.62365063C>T, NM_001134758.2:c.-25846G>A (ARFRP1))

Chromosome 20
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.62365063C>T
DNA change (hg38) g.63733711C>T
Published as ZGPAT(NM_001083113.1):c.843C>T (p.(=))
ISCN -
DB-ID ZGPAT_000001
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) 0.00027 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 2020-07-16 21:50:16 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ZGPAT NM_001083113.1 ?/. - c.843C>T r.(?) p.(Asp281=)
ARFRP1 NM_001134758.2 ?/. - c.-25846G>A r.(?) p.(=)
LIME1 NM_017806.2 ?/. - c.-3019C>T r.(?) p.(=)


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