Variant #0000677723 (NC_000006.11:g.31692386C>G, NM_013974.1:c.*2628G>C (DDAH2))

Chromosome 6
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.31692386C>G
DNA change (hg38) -
Published as C6orf25(NM_025260.3):c.523C>G (p.(Arg175Gly)), MPIG6B(NM_025260.3):c.523C>G (p.R175G)
ISCN -
DB-ID C6orf25_000004 See all 2 reported entries
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) 0.04191 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2023-07-07 10:10:56 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DDAH2 NM_013974.1 -?/. - c.*2628G>C r.(=) p.(=)
LY6G6C NM_025261.2 -?/. - c.-2930G>C r.(?) p.(=)
C6orf25 NM_138272.2 -?/. - c.523C>G r.(?) p.(Arg175Gly)


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