Variant #0000299167 (NC_000019.9:g.36236909G>C, NM_014727.1:c.*7451G>C (KMT2B))

Chromosome 19
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.36236909G>C
DNA change (hg38) g.35746008G>C
Published as PSENEN(NM_001281532.3):c.61+17G>C, PSENEN(NM_172341.3):c.61+17G>C, PSENEN(NM_172341.4):c.61+17G>C
ISCN -
DB-ID PSENEN_000003 See all 3 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) 0.15883 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2025-02-07 18:57:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KMT2B NM_014727.1 -/. - c.*7451G>C r.(=) p.(=)
LIN37 NM_019104.2 -/. - c.-2717G>C r.(?) p.(=)
IGFLR1 NM_024660.2 -/. - c.-3656C>G r.(?) p.(=)
U2AF1L4 NM_144987.2 -/. - c.-617C>G r.(?) p.(=)
PSENEN NM_172341.1 -/. - c.61+17G>C r.(=) p.(=)


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