Variant #0000689695 (NC_000006.11:g.31692533C>G, NM_013974.1:c.*2481G>C (DDAH2))

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.31692533C>G
DNA change (hg38) -
Published as -
ISCN -
DB-ID C6orf25_000005
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) 8.0E-5 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2020-09-15 15:50:26 +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     
DDAH2 NM_013974.1 ?/. - c.*2481G>C r.(=) p.(=)
LY6G6C NM_025261.2 ?/. - c.-3077G>C r.(?) p.(=)
C6orf25 NM_138272.2 ?/. - c.542-9C>G r.(=) p.(=)


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