Variant #0000530621 (NC_000007.13:g.128037043C>T, NM_000883.3:c.1108G>A (IMPDH1))

Chromosome 7
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.128037043C>T
DNA change (hg38) g.128396989C>T
Published as IMPDH1(NM_000883.3):c.1108G>A (p.A370T), IMPDH1(NM_000883.4):c.1108G>A (p.A370T)
ISCN -
DB-ID IMPDH1_000013 See all 5 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) 0.00189 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 2019-07-18 18:22:55 +02:00 (CEST)
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     
IMPDH1 NM_000883.3 -?/. - c.1108G>A r.(?) p.(Ala370Thr)


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