Variant #0000718724 (NC_000002.11:g.27440760T>G, NM_004341.3:c.98T>G (CAD))

Chromosome 2
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.27440760T>G
DNA change (hg38) -
Published as CAD(NM_004341.5):c.98T>G (p.M33R)
ISCN -
DB-ID ATRAID_000001
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 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2021-02-08 18:36:18 +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     
CAD NM_004341.3 +?/. - c.98T>G r.(?) p.(Met33Arg)
ATRAID NM_016085.4 +?/. - c.*944T>G r.(=) p.(=)
SLC5A6 NM_021095.2 +?/. - c.-6080A>C r.(?) p.(=)


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