chr22:22127164:C>T Detail (hg19) (MAPK1)

Information

Genome

Assembly Position
hg19 chr22:22,127,164-22,127,164
hg38 chr22:21,772,875-21,772,875 View the variant detail on this assembly version.

HGVS

Type Transcript Protein
RefSeq NM_138957.3:c.964G>A NP_620407.1:p.Glu322Lys
NM_002745.4:c.964G>A NP_002736.3:p.Glu322Lys
Ensemble ENST00000398822.7:c.964G>A ENST00000398822.7:p.Glu322Lys
Summary

MGeND

Clinical significance not provided
Variant entry 4
GWAS entry
Disease area statistics Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance Likely pathogenic
Review star
Show details
Links
Type Database ID Link
Gene MIM 176948 OMIM
HGNC 6871 HGNC
Ensembl ENSG00000100030 Ensembl
NCBI NCBI
Gene Cards Gene Cards
OncoKB OncoKB
Type Database ID Link
Variant TogoVar
COSMIC COSM461148 COSMIC
MONDO
Disease area statistics
MGeND
Clinical significance Last evaluated Condition Origin Submission ID Submitter Institute Citation Comment Image
not provided body of stomach not provided MGS000041
(TMGS000094)
Hitoshi Nakagama National Cancer Center Japan
not provided intrahepatic bile duct carcinoma not provided MGS000041
(TMGS000094)
Hitoshi Nakagama National Cancer Center Japan
not provided pyloric antrum not provided MGS000042
(TMGS000093)
Hitoshi Nakagama National Cancer Center Japan
not provided bronchus or lung, unspecified not provided MGS000042
(TMGS000093)
Hitoshi Nakagama National Cancer Center Japan
ClinVar
Clinical significance Last evaluated Review status Condition Origin Links
Likely pathogenic 2016-05-31 no assertion criteria provided Neoplasm of uterine cervix somatic Detail
Likely pathogenic 2016-05-31 no assertion criteria provided Squamous cell carcinoma of the head and neck somatic Detail
Likely pathogenic 2016-05-31 no assertion criteria provided somatic Detail
CIViC
Disease Drug EL ET ED CS VO TR Pubmed Links
head and neck squamous cell carcinoma Erlotinib C Predictive Supports Sensitivity/Response Somatic 4 26181029 Detail
DisGeNET
[No Data.]
Annotation

Annotations

DescrptionSourceLinks
Case report of a patient with stage IVA HNSCC with near-complete histologic response after 13 days o... CIViC Evidence Detail
NM_002745.5(MAPK1):c.964G>A (p.Glu322Lys) AND Neoplasm of uterine cervix ClinVar Detail
NM_002745.5(MAPK1):c.964G>A (p.Glu322Lys) AND Squamous cell carcinoma of the head and neck ClinVar Detail
NM_002745.5(MAPK1):c.964G>A (p.Glu322Lys) AND Transitional cell carcinoma of the bladder ClinVar 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
rs1057519911 dbSNP
Genome
hg19
Position
chr22:22,127,164-22,127,164
Variant Type
snv
Reference Allele
C
Alternative Allele
T
Variant (CIViC) (CIViC Variant)
E322K
Transcript 1 (CIViC Variant)
ENST00000215832.6
Variant URL (CIViC Variant)
https://civic.genome.wustl.edu/links/variants/320
Genome browser