Variant #0000888098 (NC_000008.10:g.102678859G>C, NM_024915.3:c.1806G>C (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.102678859G>C
DNA change (hg38) -
Published as GRHL2(NM_001330593.1):c.1758G>C (p.S586=), GRHL2(NM_024915.3):c.1806G>C (p.S602=), GRHL2(NM_024915.4):c.1806G>C (p.S602=)
ISCN -
DB-ID GRHL2_000004 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) 0.00171 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 2022-11-01 13:01:21 +01:00 (CET)
Date last edited 2024-02-26 20:06:56 +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.1806G>C r.(?) p.(Ser602=)


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