Variant #0000281079 (NC_000016.9:g.4386814T>C, NM_032575.2:c.864T>C (GLIS2))

Chromosome 16
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.4386814T>C
DNA change (hg38) g.4336813T>C
Published as GLIS2(NM_032575.3):c.864T>C (p.Y288=)
ISCN -
DB-ID GLIS2_000005 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) 0.9795 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CORO7-PAM16 NM_001201479.1 -/. - c.*3506A>G r.(=) p.(=)
PAM16 NM_016069.9 -/. - c.*3506A>G r.(=) p.(=)
CORO7 NM_024535.4 -/. - c.*18345A>G r.(=) p.(=)
GLIS2 NM_032575.2 -/. - c.864T>C r.(?) p.(Tyr288=)
VASN NM_138440.2 -/. - c.-35190T>C r.(?) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.