Variant #0000962818 (NC_000003.11:g.49042318G>A, NM_177938.2:c.912G>A (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.49042318G>A
DNA change (hg38) -
Published as P4HTM(NM_177938.2):c.912G>A (p.S304=)
ISCN -
DB-ID P4HTM_000012
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) 0.00012 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 2024-02-26 20:06:56 +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.*10703C>T r.(=) p.(=)
WDR6 NM_018031.3 -?/. - c.-2457G>A r.(?) p.(=)
P4HTM NM_177938.2 -?/. - c.912G>A r.(?) p.(Ser304=)


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