Variant #0001034986 (NC_000005.9:g.147449923G>C, NM_001127698.1:c.119G>C (SPINK5))

Chromosome 5
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.147449923G>C
DNA change (hg38) -
Published as SPINK5(NM_006846.3):c.119G>C (p.G40A), SPINK5(NM_006846.4):c.119G>C (p.(Gly40Ala))
ISCN -
DB-ID SPINK5_000097 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) 0.00274 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 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     
SPINK5 NM_001127698.1 -/. - c.119G>C r.(?) p.(Gly40Ala)


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