NEXMIF p.Gln705Ter (p.Q705*) Detail (hg19) (NEXMIF)

Information

Genome

Assembly Position
hg19 chrX:73,962,279-73,962,279
hg38 chrX:74,742,444-74,742,444 View the variant detail on this assembly version.

HGVS

Type Transcript Protein
RefSeq NM_001008537.2:c.2113C>T NP_001008537.1:p.Gln705Ter
Ensemble ENST00000055682.12:c.2113C>T ENST00000055682.12:p.Gln705Ter
ENST00000616200.2:c.2113C>T ENST00000616200.2:p.Gln705Ter
Summary

MGeND

Clinical significance Pathogenic
Variant entry 1
GWAS entry
Disease area statistics Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance
Review star [No Data.]
Show details
Links
Type Database ID Link
Gene MIM 300524 OMIM
HGNC 29433 HGNC
Ensembl ENSG00000050030 Ensembl
NCBI NCBI
Gene Cards Gene Cards
OncoKB OncoKB
Type Database ID Link
Variant TogoVar
COSMIC
MONDO
Disease area statistics
MGeND
Clinical significance Last evaluated Condition Origin Submission ID Submitter Institute Citation Comment Image
Pathogenic other germline MGS000001
(TMGS000137) 		Kenjiro Kosaki Keio University
ClinVar
[No Data.]
CIViC
[No Data.]
DisGeNET
[No Data.]
Annotation

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
-
Genome
hg19
Position
chrX:73,962,279-73,962,279
Variant Type
snv
Reference Allele
G
Alternative Allele
A
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