Variant #0000857047 (NC_000001.10:g.156028138C>T, NM_020387.2:c.-3054C>T (RAB25))

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.156028138C>T
DNA change (hg38) -
Published as LAMTOR2(NM_014017.3):c.354C>T (p.P118=)
ISCN -
DB-ID LAMTOR2_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) 7.0E-5 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     
LAMTOR2 NM_014017.3 -?/. - c.354C>T r.(?) p.(Pro118=)
UBQLN4 NM_020131.3 -?/. - c.-4646G>A r.(?) p.(=)
RAB25 NM_020387.2 -?/. - c.-3054C>T r.(?) p.(=)


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