Variant #0000297168 (NC_000007.13:g.6045634T>C, NM_000535.6:c.52A>G (PMS2))

Chromosome 7
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.6045634T>C
DNA change (hg38) g.6006003T>C
Published as PMS2(NM_000535.5):c.52A>G (p.(Ile18Val), p.I18V), PMS2(NM_000535.7):c.52A>G (p.I18V)
ISCN -
DB-ID PMS2_000009 See all 23 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) 0.00906 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PMS2 NM_000535.6 -/. - c.52A>G r.(?) p.(Ile18Val)
AIMP2 NM_006303.3 -/. - c.-3361T>C r.(?) p.(=)
EIF2AK1 NM_014413.3 -/. - c.*18670A>G r.(=) p.(=)


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