Variant #0001036471 (NC_000007.13:g.6045633A>G, NM_000535.6:c.53T>C (PMS2))

Chromosome 7
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.6045633A>G
DNA change (hg38) -
Published as PMS2(NM_000535.7):c.53T>C (p.I18T)
ISCN -
DB-ID PMS2_000295 See all 5 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) 0.00036 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PMS2 NM_000535.6 ?/. - c.53T>C r.(?) p.(Ile18Thr)
AIMP2 NM_006303.3 ?/. - c.-3362A>G r.(?) p.(=)
EIF2AK1 NM_014413.3 ?/. - c.*18671T>C r.(=) p.(=)


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