Variant #0000506749 (NC_000001.10:g.24646241_24646244del, NM_021180.3:c.-3335_-3332del (GRHL3))

Chromosome 1
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.24646241_24646244del
DNA change (hg38) g.24319751_24319754del
Published as GRHL3(NM_001195010.2):c.-122+4_-122+7del
ISCN -
DB-ID GRHL3_000030
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GRHL3 NM_021180.3 -?/. - c.-3335_-3332del r.(?) p.(=)
STPG1 NM_178122.4 -?/. - c.*38792_*38795del r.(=) p.(=)


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