Variant #0000533339 (NC_000008.10:g.102585965C>T, NM_024915.3:c.804C>T (GRHL2))

Chromosome 8
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.102585965C>T
DNA change (hg38) g.101573737C>T
Published as GRHL2(NM_001330593.1):c.756C>T (p.T252=), GRHL2(NM_024915.4):c.804C>T (p.T268=)
ISCN -
DB-ID GRHL2_000015 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) 0.00074 View details
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 2022-11-01 13:01:21 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GRHL2 NM_024915.3 -?/. - c.804C>T r.(?) p.(Thr268=)


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