Variant #0000520153 (NC_000003.11:g.49051200A>G, NM_177938.2:c.*6860A>G (P4HTM))

Chromosome 3
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.49051200A>G
DNA change (hg38) g.49013767A>G
Published as WDR6(NM_001320546.2):c.2155A>G (p.T719A)
ISCN -
DB-ID P4HTM_000006
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) 4.0E-5 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-10-29 20:49:11 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DALRD3 NM_001009996.2 ?/. - c.*1821T>C r.(=) p.(=)
WDR6 NM_018031.3 ?/. - c.2323A>G r.(?) p.(Thr775Ala)
P4HTM NM_177938.2 ?/. - c.*6860A>G r.(=) p.(=)


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