Variant #0000610261 (NC_000006.11:g.31691666C>A, NM_013974.1:c.*3348G>T (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.31691666C>A
DNA change (hg38) g.31723889C>A
Published as C6orf25(NM_025260.3):c.312C>A (p.(Gly104=))
ISCN -
DB-ID C6orf25_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) 0.00997 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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2022-05-09 15:51:19 +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.*3348G>T r.(=) p.(=)
LY6G6C NM_025261.2 -?/. - c.-2210G>T r.(?) p.(=)
C6orf25 NM_138272.2 -?/. - c.312C>A r.(?) p.(Gly104=)


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