Variant #0000807408 (NC_000016.9:g.4385366C>T, NM_032575.2:c.747C>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.4385366C>T
DNA change (hg38) -
Published as GLIS2(NM_001318918.1):c.747C>T (p.N249=)
ISCN -
DB-ID CORO7_000016
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CORO7-PAM16 NM_001201479.1 -?/. - c.*4954G>A r.(=) p.(=)
PAM16 NM_016069.9 -?/. - c.*4954G>A r.(=) p.(=)
CORO7 NM_024535.4 -?/. - c.*19793G>A r.(=) p.(=)
GLIS2 NM_032575.2 -?/. - c.747C>T r.(?) p.(Asn249=)
VASN NM_138440.2 -?/. - c.-36638C>T r.(?) p.(=)


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