chrX:44929415:AACA> Detail (hg19) (KDM6A)

Information

Genome

Assembly Position
hg19 chrX:44,929,415-44,929,418
hg38 chrX:45,070,170-45,070,173 

HGVS

Type Transcript Protein
RefSeq NM_021140.3:c.2515_2518delAACA NP_066963.2:p.Asn839ValfsTer27
NM_001291416.1:c.2536_2539delAACA NP_001278345.1:p.Asn846ValfsTer27
NM_001291417.1:c.2380_2383delAACA NP_001278346.1:p.Asn794ValfsTer27
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance Pathogenic
Review star
Show details
Links
Type Database ID Link
Gene MIM 300128 OMIM
HGNC 12637 HGNC
Ensembl ENSG00000147050 Ensembl
NCBI NCBI
Gene Cards Gene Cards
OncoKB OncoKB
Type Database ID Link
Variant TogoVar
COSMIC COSM5711655 COSMIC
MONDO
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
Clinical significance Last evaluated Review status Condition Origin Links
Pathogenic 2014-05-01 no assertion criteria provided Kabuki syndrome 2 germline Detail
Pathogenic 2018-12-31 criteria provided, single submitter not provided germline Detail
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
0.120 Kabuki syndrome 2 NA CLINVAR Detail
Annotation

Annotations

DescrptionSourceLinks
NM_001291415.2(KDM6A):c.2671_2674del (p.Asn891fs) AND Kabuki syndrome 2 ClinVar Detail
NM_001291415.2(KDM6A):c.2671_2674del (p.Asn891fs) AND not provided ClinVar Detail
NA DisGeNET Detail

Overlapped Transcript Coordinates

Gene Transcript ID Exon Number Chromosome Start Stop Type Amino Mutation Transcript Position Links

Overlapped Transcript

Gene Transcript ID Chromosome Start Stop Links
Gene
-
dbSNP
rs786205676 dbSNP
Genome
hg19
Position
chrX:44,929,415-44,929,418
Variant Type
snv
Reference Allele
AACA
Alternative Allele
-
Genome browser