Variant #0000571423 (NC_000022.10:g.20779768G>C, NM_182895.2:c.2495C>G (SCARF2))

Chromosome 22
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.20779768G>C
DNA change (hg38) g.20425478G>C
Published as SCARF2(NM_153334.7):c.2510C>G (p.P837R), SCARF2(NM_153334.7):c.2513C>G (p.A838G)
ISCN -
DB-ID SCARF2_000023 See all 2 reported entries
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) 0.54917 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SCARF2 NM_182895.2 -/. - c.2495C>G r.(?) p.(Ala832Gly)


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