Variant #0000555606 (NC_000015.9:g.81598492G>A, NM_172217.3:c.3664G>A (IL16))

Chromosome 15
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.81598492G>A
DNA change (hg38) g.81306151G>A
Published as IL16(NM_001172128.1):c.3664G>A (p.V1222I)
ISCN -
DB-ID IL16_000005
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) 0.00013 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IL16 NM_172217.3 -?/. - c.3664G>A r.(?) p.(Val1222Ile)
STARD5 NM_181900.2 -?/. - c.*7105C>T r.(=) p.(=)


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