Variant #0000913165 (NC_000009.11:g.37436644_37436649del, NC_000009.11(NM_012203.1):c.866-14_866-9del (GRHPR))

Chromosome 9
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.37436644_37436649del
DNA change (hg38) -
Published as GRHPR(NM_012203.2):c.866-14_866-9delTCTCTC
ISCN -
DB-ID GRHPR_000023
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-01-11 15:44:22 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GRHPR NM_012203.1 -?/. - c.866-14_866-9del r.(=) p.(=)
ZBTB5 NM_014872.2 -?/. - c.*3877_*3882del r.(=) p.(=)


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