Variant #0000324549 (NC_000016.9:g.4387382G>A, NM_032575.2:c.1432G>A (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.4387382G>A
DNA change (hg38) g.4337381G>A
Published as GLIS2(NM_032575.2):c.1432G>A (p.(Asp478Asn))
ISCN -
DB-ID GLIS2_000008
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
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.*2938C>T r.(=) p.(=)
PAM16 NM_016069.9 ?/. - c.*2938C>T r.(=) p.(=)
CORO7 NM_024535.4 ?/. - c.*17777C>T r.(=) p.(=)
GLIS2 NM_032575.2 ?/. - c.1432G>A r.(?) p.(Asp478Asn)
VASN NM_138440.2 ?/. - c.-34622G>A r.(?) p.(=)


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