Variant #0000611363 (NC_000008.10:g.102505093_102505098del, NC_000008.10(NM_024915.3):c.20+76_20+81del (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.102505093_102505098del
DNA change (hg38) g.101492865_101492870del
Published as GRHL2(NM_001330593.1):c.-29+16_-29+21delGTTTTT
ISCN -
DB-ID GRHL2_000020
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +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.20+76_20+81del r.(=) p.(=)


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