Variant #0000857615 (NC_000001.10:g.8421875G>A, NM_001042681.1:c.1964C>T (RERE))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.8421875G>A
DNA change (hg38) -
Published as RERE(NM_001042681.1):c.1964C>T (p.(Ala655Val)), RERE(NM_012102.3):c.1964C>T (p.A655V)
ISCN -
DB-ID RERE_000024 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) 0.00023 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 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RERE NM_001042681.1 -?/. - c.1964C>T r.(?) p.(Ala655Val)


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