Variant #0000724842 (NC_000014.8:g.66975271C>G, NM_020806.4:c.26C>G (GPHN))

Chromosome 14
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.66975271C>G
DNA change (hg38) -
Published as GPHN(NM_001024218.1):c.26C>G (p.(Thr9Ser)), GPHN(NM_020806.4):c.26C>G (p.T9S), GPHN(NM_020806.5):c.26C>G (p.T9S)
ISCN -
DB-ID GPHN_000001 See all 4 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) 0.00135 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GPHN NM_020806.4 -?/. - c.26C>G r.(?) p.(Thr9Ser)


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