chr11:67258349:AG>GT Detail (hg19) (AIP)

Information

Genome

Assembly Position
hg19 chr11:67,258,349-67,258,350
hg38 chr11:67,490,878-67,490,879 View the variant detail on this assembly version.

HGVS

Type Transcript Protein
RefSeq NM_001302959.1:c.878_879delinsGT NP_001289888.1:p.Glu293Gly
NM_001302960.1:c.878_879delinsGT NP_001289889.1:p.Glu293Gly
NM_003977.3:c.878_879delinsGT NP_003968.3:p.Glu293Gly
Summary

MGeND

Clinical significance
Variant entry
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 605555 OMIM
HGNC 358 HGNC
Ensembl ENSG00000110711 Ensembl
NCBI NCBI
Gene Cards Gene Cards
OncoKB OncoKB
Type Database ID Link
Variant TogoVar
COSMIC
MONDO
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
[No Data.]
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
0.241 Growth Hormone-Secreting Pituitary Adenoma NA CLINVAR Detail
Annotation

Annotations

DescrptionSourceLinks
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
rs267606583 dbSNP
Genome
hg19
Position
chr11:67,258,349-67,258,350
Variant Type
snv
Reference Allele
AG
Alternative Allele
GT
Genome browser