Variant #0000993768 (NC_000003.11:g.49042515T>G, NM_177938.2:c.1109T>G (P4HTM))

Chromosome 3
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.49042515T>G
DNA change (hg38) -
Published as P4HTM(NM_177938.2):c.1109T>G (p.L370R)
ISCN -
DB-ID P4HTM_000014
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) 0.00044 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2024-08-28 13:16:32 +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.*10506A>C r.(=) p.(=)
WDR6 NM_018031.3 -?/. - c.-2260T>G r.(?) p.(=)
P4HTM NM_177938.2 -?/. - c.1109T>G r.(?) p.(Leu370Arg)


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