Variant #0000608141 (NC_000002.11:g.86444180C>A, NM_022912.2:c.*43G>T (REEP1))

Chromosome 2
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.86444180C>A
DNA change (hg38) g.86217057C>A
Published as REEP1(NM_001164732.2):c.414G>T (p.S138=), REEP1(NM_001371279.1):c.837G>T (p.S279=)
ISCN -
DB-ID REEP1_000006 See all 15 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) 0.00077 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 2019-12-04 14:54:23 +01:00 (CET)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MRPL35 NM_016622.3 -/. - c.*6389C>A r.(=) p.(=)
REEP1 NM_022912.2 -/. - c.*43G>T r.(=) p.(=)


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