Variant #0000801875 (NC_000005.9:g.131534046_131534047del, NC_000005.9(NM_004199.2):c.1306-81_1306-80del (P4HA2))

Chromosome 5
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.131534046_131534047del
DNA change (hg38) -
Published as P4HA2(NM_001017973.1):c.1334_1335delAG (p.E445Gfs*3), P4HA2(NM_004199.2):c.1306-81_1306-80delAG
ISCN -
DB-ID P4HA2_000006
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2024-02-26 20:06:56 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
P4HA2 NM_004199.2 ?/. - c.1306-81_1306-80del r.(=) p.(=)


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