Variant #0000524699 (NC_000005.9:g.147207678T>C, NM_003122.3:c.101A>G (SPINK1))

Chromosome 5
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.147207678T>C
DNA change (hg38) g.147828115T>C
Published as SPINK1(NM_001379610.1):c.101A>G (p.(Asn34Ser)), SPINK1(NM_003122.4):c.101A>G (p.N34S), SPINK1(NM_003122.5):c.101A>G (p.N34S)
ISCN -
DB-ID SPINK1_000002 See all 12 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) 0.00915 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SPINK1 NM_003122.3 ?/. - c.101A>G r.(?) p.(Asn34Ser)


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