Variant #0000329401 (NC_000003.11:g.49055837C>G, NM_177938.2:c.*11497C>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.49055837C>G
DNA change (hg38) g.49018404C>G
Published as DALRD3(NM_001009996.2):c.161G>C (p.(Gly54Ala))
ISCN -
DB-ID DALRD3_000002
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) 1.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-10-29 21:08:56 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DALRD3 NM_001009996.2 ?/. - c.161G>C r.(?) p.(Gly54Ala)
WDR6 NM_018031.3 ?/. - c.*3116C>G r.(=) p.(=)
P4HTM NM_177938.2 ?/. - c.*11497C>G r.(=) p.(=)
NDUFAF3 NM_199069.1 ?/. - c.-3741C>G r.(?) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.