Variant #0000719083 (NC_000002.11:g.86444174G>A, NM_022912.2:c.*49C>T (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.86444174G>A
DNA change (hg38) -
Published as REEP1(NM_001164732.2):c.420C>T (p.T140=)
ISCN -
DB-ID MRPL35_000003
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) 0.00012 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 2021-02-08 18:36:18 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MRPL35 NM_016622.3 -?/. - c.*6383G>A r.(=) p.(=)
REEP1 NM_022912.2 -?/. - c.*49C>T r.(=) p.(=)


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