Variant #0000245490 (NC_000001.10:g.111661412A>G, NC_000001.10(NM_178454.4):c.693+15T>C (DRAM2))

Chromosome 1
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.111661412A>G
DNA change (hg38) g.111118790A>G
Published as DRAM2(NM_178454.6):c.693+15T>C
ISCN -
DB-ID DRAM2_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) 0.00044 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +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.-21591A>G r.(?) p.(=)
DRAM2 NM_178454.4 -/. - c.693+15T>C r.(=) p.(=)


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