Variant #0001040622 (NC_000015.9:g.81517844C>G, NM_172217.3:c.104C>G (IL16))

Chromosome 15
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.81517844C>G
DNA change (hg38) -
Published as IL16(NM_172217.5):c.104C>G (p.(Ser35Cys))
ISCN -
DB-ID IL16_000008
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 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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IL16 NM_172217.3 ?/. - c.104C>G r.(?) p.(Ser35Cys)
STARD5 NM_181900.2 ?/. - c.*87753G>C r.(=) p.(=)


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