Variant #0000883347 (NC_000001.10:g.24673119G>A, NM_021180.3:c.1546G>A (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.24673119G>A
DNA change (hg38) -
Published as GRHL3(NM_198173.2):c.1531G>A (p.(Asp511Asn)), GRHL3(NM_198174.3):c.1531G>A (p.D511N)
ISCN -
DB-ID GRHL3_000044 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) 0.00051 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2022-11-01 13:01:21 +01:00 (CET)
Date last edited 2024-08-28 13:07:21 +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.1546G>A r.(?) p.(Asp516Asn)
STPG1 NM_178122.4 -?/. - c.*11914C>T r.(=) p.(=)


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