Variant #0000864811 (NC_000016.9:g.4391476G>A, NM_032575.2:c.*3951G>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.4391476G>A
DNA change (hg38) -
Published as CORO7-PAM16(NM_001201479.1):c.2887C>T (p.(Arg963Cys)), PAM16(NM_016069.10):c.118C>T (p.R40C)
ISCN -
DB-ID CORO7_000020 See all 2 reported entries
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) 0.00016 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 2022-05-09 16:01:56 +02:00 (CEST)
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.2887C>T r.(?) p.(Arg963Cys)
PAM16 NM_016069.9 ?/. - c.118C>T r.(?) p.(Arg40Cys)
CORO7 NM_024535.4 ?/. - c.*13683C>T r.(=) p.(=)
GLIS2 NM_032575.2 ?/. - c.*3951G>A r.(=) p.(=)
VASN NM_138440.2 ?/. - c.-30528G>A r.(?) p.(=)


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