Variant #0000315603 (NC_000005.9:g.147494001G>A, NM_001127698.1:c.1964G>A (SPINK5))

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.147494001G>A
DNA change (hg38) g.148114438G>A
Published as SPINK5(NM_001127698.1):c.1964G>A (p.G655D, p.(Gly655Asp)), SPINK5(NM_006846.4):c.1964G>A (p.G655D)
ISCN -
DB-ID SPINK5_000031 See all 3 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) 0.00267 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SPINK5 NM_001127698.1 ?/. - c.1964G>A r.(?) p.(Gly655Asp)


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