Variant #0000287105 (NC_000002.11:g.242432819G>A, NM_014808.2:c.3007G>A (FARP2))

Chromosome 2
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.242432819G>A
DNA change (hg38) g.241493404G>A
Published as FARP2(NM_014808.4):c.3007G>A (p.V1003I)
ISCN -
DB-ID FARP2_000003
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) 0.00016 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
STK25 NM_006374.3 ?/. - c.*2258C>T r.(=) p.(=)
FARP2 NM_014808.2 ?/. - c.3007G>A r.(?) p.(Val1003Ile)


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