Variant #0000992658 (NC_000002.11:g.233394675C>T, NM_000751.2:c.646C>T (CHRND))

Chromosome 2
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.233394675C>T
DNA change (hg38) -
Published as CHRND(NM_000751.2):c.646C>T (p.(Arg216Trp))
ISCN -
DB-ID CHRND_000077
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) 0.00023 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 2024-08-28 13:07:21 +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     
CHRND NM_000751.2 -?/. - c.646C>T r.(?) p.(Arg216Trp)
PRSS56 NM_001195129.1 -?/. - c.*4459C>T r.(=) p.(=)


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