Variant #0001036299 (NC_000007.13:g.16445874G>A, NM_001101426.3:c.346C>T (ISPD))

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.16445874G>A
DNA change (hg38) -
Published as CRPPA(NM_001101426.4):c.346C>T (p.R116C), ISPD(NM_001101426.3):c.346C>T (p.R116C)
ISCN -
DB-ID ISPD_000102 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) 0.00128 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2025-05-05 21:14:00 +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     
ISPD NM_001101426.3 -?/. - c.346C>T r.(?) p.(Arg116Cys)


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