Variant #0000319191 (NC_000019.9:g.36235225T>C, NM_014727.1:c.*5767T>C (KMT2B))

Chromosome 19
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.36235225T>C
DNA change (hg38) g.35744324T>C
Published as U2AF1L4(NM_001040425.3):c.230A>G (p.K77R)
ISCN -
DB-ID U2AF1L4_000001
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 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 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KMT2B NM_014727.1 ?/. - c.*5767T>C r.(=) p.(=)
LIN37 NM_019104.2 ?/. - c.-4401T>C r.(?) p.(=)
IGFLR1 NM_024660.2 ?/. - c.-1972A>G r.(?) p.(=)
U2AF1L4 NM_144987.2 ?/. - c.230A>G r.(?) p.(Lys77Arg)
PSENEN NM_172341.1 ?/. - c.-1473T>C r.(?) p.(=)


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