Variant #0000502447 (NC_000001.10:g.111663218A>C, NM_178454.4:c.437T>G (DRAM2))

Chromosome 1
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.111663218A>C
DNA change (hg38) g.111120596A>C
Published as DRAM2(NM_178454.5):c.437T>G (p.M146R)
ISCN -
DB-ID CEPT1_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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CEPT1 NM_006090.3 ?/. - c.-19785A>C r.(?) p.(=)
DRAM2 NM_178454.4 ?/. - c.437T>G r.(?) p.(Met146Arg)


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