Variant #0000851099 (NC_000006.11:g.151742458_151742459insCAT, NC_000006.11(NM_017909.3):c.1003-2_1003-1insTGA (RMND1))

Chromosome 6
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.151742458_151742459insCAT
DNA change (hg38) -
Published as RMND1(NM_017909.4):c.1003-2_1003-1insTGA
ISCN -
DB-ID RMND1_000023
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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2022-05-09 15:40:45 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RMND1 NM_017909.3 ?/. - c.1003-2_1003-1insTGA r.spl? p.?


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