Variant #0000305977 (NC_000007.13:g.6045549C>A, NM_000535.6:c.137G>T (PMS2))

Chromosome 7
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.6045549C>A
DNA change (hg38) g.6005918C>A
Published as PMS2(NM_000535.5):c.137G>T (p.S46I, p.(Ser46Ile)), PMS2(NM_000535.7):c.137G>T (p.S46I)
ISCN -
DB-ID PMS2_000061 See all 40 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) 0.00016 View details
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 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PMS2 NM_000535.6 +?/. - c.137G>T r.(?) p.(Ser46Ile)
AIMP2 NM_006303.3 +?/. - c.-3446C>A r.(?) p.(=)
EIF2AK1 NM_014413.3 +?/. - c.*18755G>T r.(=) p.(=)


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