Variant #0001014346 (NC_000007.13:g.31016038C>A, NC_000007.13(NM_000823.3):c.975-6C>A (GHRHR))

Chromosome 7
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.31016038C>A
DNA change (hg38) -
Published as GHRHR(NM_000823.3):c.975-6C>A (p.(=)), GHRHR(NM_000823.4):c.975-6C>A
ISCN -
DB-ID GHRHR_000038 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) 0.00084 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 2024-10-29 21:08:56 +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     
GHRHR NM_000823.3 -?/. - c.975-6C>A r.(=) p.(=)


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