Variant #0000558222 (NC_000016.9:g.4387338C>T, NM_032575.2:c.1388C>T (GLIS2))

Chromosome 16
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.4387338C>T
DNA change (hg38) g.4337337C>T
Published as GLIS2(NM_032575.2):c.1388C>T (p.T463M)
ISCN -
DB-ID CORO7_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) 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 2019-07-18 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     
CORO7-PAM16 NM_001201479.1 ?/. - c.*2982G>A r.(=) p.(=)
PAM16 NM_016069.9 ?/. - c.*2982G>A r.(=) p.(=)
CORO7 NM_024535.4 ?/. - c.*17821G>A r.(=) p.(=)
GLIS2 NM_032575.2 ?/. - c.1388C>T r.(?) p.(Thr463Met)
VASN NM_138440.2 ?/. - c.-34666C>T r.(?) p.(=)


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