Variant #0000892993 (NC_000016.9:g.4385414C>T, NC_000016.9(NM_032575.2):c.775+20C>T (GLIS2))

Chromosome 16
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.4385414C>T
DNA change (hg38) -
Published as GLIS2(NM_032575.2):c.775+20C>T
ISCN -
DB-ID CORO7_000024
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) 0.00115 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-11-01 13:41:49 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CORO7-PAM16 NM_001201479.1 -?/. - c.*4906G>A r.(=) p.(=)
PAM16 NM_016069.9 -?/. - c.*4906G>A r.(=) p.(=)
CORO7 NM_024535.4 -?/. - c.*19745G>A r.(=) p.(=)
GLIS2 NM_032575.2 -?/. - c.775+20C>T r.(=) p.(=)
VASN NM_138440.2 -?/. - c.-36590C>T r.(?) p.(=)


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