Variant #0000719489 (NC_000003.11:g.49041570G>A, NM_177938.2:c.764G>A (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.49041570G>A
DNA change (hg38) -
Published as P4HTM(NM_177938.2):c.764G>A (p.R255Q)
ISCN -
DB-ID P4HTM_000007
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
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.*11451C>T r.(=) p.(=)
WDR6 NM_018031.3 ?/. - c.-3205G>A r.(?) p.(=)
P4HTM NM_177938.2 ?/. - c.764G>A r.(?) p.(Arg255Gln)


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