Variant #0000306129 (NC_000006.11:g.43581405_43581407del, NM_006502.2:c.1253_1255del (POLH))

Chromosome 6
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.43581405_43581407del
DNA change (hg38) g.43613668_43613670del
Published as POLH(NM_006502.2):c.1253_1255delCTC (p.P418del), POLH(NM_006502.3):c.1253_1255delCTC (p.P418del)
ISCN -
DB-ID POLH_000019 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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
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     
POLH NM_006502.2 ?/. - c.1253_1255del r.(?) p.(Pro418del)
GTPBP2 NM_019096.3 ?/. - c.*7950_*7952del r.(=) p.(=)


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