Variant #0000524697 (NC_000005.9:g.147207585C>T, NM_003122.3:c.194G>A (SPINK1))

Chromosome 5
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.147207585C>T
DNA change (hg38) g.147828022C>T
Published as SPINK1(NM_003122.3):c.194G>A (p.(Arg65Gln)), SPINK1(NM_003122.4):c.194G>A (p.R65Q), SPINK1(NM_003122.5):c.194G>A (p.R65Q)
ISCN -
DB-ID SPINK1_000006 See all 4 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) 0.00054 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2025-02-07 18:57:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SPINK1 NM_003122.3 +?/. - c.194G>A r.(?) p.(Arg65Gln)


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