Variant #0000719490 (NC_000003.11:g.49042355del, NM_177938.2:c.949del (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.49042355del
DNA change (hg38) -
Published as P4HTM(NM_177938.2):c.949delG (p.V317Ffs*30)
ISCN -
DB-ID P4HTM_000001 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) Retrieve
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2021-02-08 18:36:18 +01:00 (CET)
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.*10666del r.(?) p.(=)
WDR6 NM_018031.3 ?/. - c.-2420del r.(?) p.(=)
P4HTM NM_177938.2 ?/. - c.949del r.(?) p.(Val317PhefsTer30)


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