Variant #0000860880 (NC_000007.13:g.6048627C>G, NC_000007.13(NM_000535.6):c.23+1G>C (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.6048627C>G
DNA change (hg38) -
Published as PMS2(NM_000535.5):c.23+1G>C (p.?)
ISCN -
DB-ID AIMP2_000015
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2022-05-09 15:51:19 +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.23+1G>C r.spl? p.?
AIMP2 NM_006303.3 +?/. - c.-368C>G r.(?) p.(=)
EIF2AK1 NM_014413.3 +?/. - c.*15677G>C r.(=) p.(=)


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