Variant #0001055422 (NC_000016.9:g.4393249A>G, NM_032575.2:c.*5724A>G (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.4393249A>G
DNA change (hg38) -
Published as PAM16(NM_016069.11):c.47T>C (p.(Val16Ala))
ISCN -
DB-ID CORO7_000037
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) 6.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +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.2816T>C r.(?) p.(Val939Ala)
PAM16 NM_016069.9 ?/. - c.47T>C r.(?) p.(Val16Ala)
CORO7 NM_024535.4 ?/. - c.*11910T>C r.(=) p.(=)
GLIS2 NM_032575.2 ?/. - c.*5724A>G r.(=) p.(=)
VASN NM_138440.2 ?/. - c.-28755A>G r.(?) p.(=)


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