Variant #0000914630 (NC_000016.9:g.4387209C>T, NM_032575.2:c.1259C>T (GLIS2))

Chromosome 16
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.4387209C>T
DNA change (hg38) -
Published as GLIS2(NM_032575.2):c.1259C>T (p.P420L)
ISCN -
DB-ID CORO7_000004
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) 0.00172 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-01-11 15:44:22 +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.*3111G>A r.(=) p.(=)
PAM16 NM_016069.9 -?/. - c.*3111G>A r.(=) p.(=)
CORO7 NM_024535.4 -?/. - c.*17950G>A r.(=) p.(=)
GLIS2 NM_032575.2 -?/. - c.1259C>T r.(?) p.(Pro420Leu)
VASN NM_138440.2 -?/. - c.-34795C>T r.(?) p.(=)


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