Variant #0000329400 (NC_000003.11:g.49055133C>T, NM_177938.2:c.*10793C>T (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.49055133C>T
DNA change (hg38) g.49017700C>T
Published as DALRD3(NM_001009996.2):c.631G>A (p.(Gly211Ser))
ISCN -
DB-ID DALRD3_000001
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) Retrieve
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)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DALRD3 NM_001009996.2 ?/. - c.631G>A r.(?) p.(Gly211Ser)
WDR6 NM_018031.3 ?/. - c.*2412C>T r.(=) p.(=)
P4HTM NM_177938.2 ?/. - c.*10793C>T r.(=) p.(=)
NDUFAF3 NM_199069.1 ?/. - c.-4445C>T r.(?) p.(=)


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