Variant #0000964279 (NC_000006.11:g.79735759T>C, NM_017934.5:c.723A>G (PHIP))

Chromosome 6
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.79735759T>C
DNA change (hg38) -
Published as PHIP(NM_017934.6):c.723A>G (p.A241=), PHIP(NM_017934.7):c.723A>G (p.A241=)
ISCN -
DB-ID PHIP_000011 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) 0.00106 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2024-02-26 20:06:56 +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     
PHIP NM_017934.5 -?/. - c.723A>G r.(?) p.(Ala241=)


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