Variant #0000616002 (NC_000016.9:g.4387507del, NM_032575.2:c.1557del (GLIS2))

Chromosome 16
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.4387507del
DNA change (hg38) g.4337506del
Published as GLIS2(NM_001318918.1):c.1557delA (p.K519Nfs*5)
ISCN -
DB-ID CORO7_000010
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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-07-09 11:48:20 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CORO7-PAM16 NM_001201479.1 +/. - c.*2815del r.(?) p.(=)
PAM16 NM_016069.9 +/. - c.*2815del r.(?) p.(=)
CORO7 NM_024535.4 +/. - c.*17654del r.(?) p.(=)
GLIS2 NM_032575.2 +/. - c.1557del r.(?) p.(Lys519AsnfsTer5)
VASN NM_138440.2 +/. - c.-34497del r.(?) p.(=)


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