Variant #0000517049 (NC_000002.11:g.86444238T>C, NC_000002.11(NM_022912.2):c.596-5A>G (REEP1))

Chromosome 2
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.86444238T>C
DNA change (hg38) g.86217115T>C
Published as REEP1(NM_022912.3):c.596-5A>G
ISCN -
DB-ID MRPL35_000002
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 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
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     
MRPL35 NM_016622.3 -?/. - c.*6447T>C r.(=) p.(=)
REEP1 NM_022912.2 -?/. - c.596-5A>G r.spl? p.?


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