Variant #0000505088 (NC_000001.10:g.213031948G>C, NM_014053.3:c.154G>C (FLVCR1))

Chromosome 1
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.213031948G>C
DNA change (hg38) g.212858606G>C
Published as FLVCR1(NM_014053.3):c.154G>C (p.A52P), FLVCR1(NM_014053.4):c.154G>C (p.A52P)
ISCN -
DB-ID FLVCR1_000002 See all 4 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) 0.48281 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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     
FLVCR1 NM_014053.3 -/. - c.154G>C r.(?) p.(Ala52Pro)


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