chr7:121941357:> Detail (hg19)

Information

Genome

Assembly Position
hg19 chr7:121,941,357-121,944,804
hg38 chr7:122,301,303-122,304,750 

HGVS

Type Transcript Protein
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

[No Data.]

Prediction

[No Data.]

ClinVar

Clinical Significance
Review star [No Data.]
Show details
Links
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
[No Data.]
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
<0.001 Malignant neoplasm of stomach NA BeFree Detail
<0.001 Neoplasm Metastasis NA BeFree Detail
<0.001 Stomach Neoplasms NA BeFree Detail
0.120 Kallmann syndrome NA BeFree,ORPHANET Detail
<0.001 Tumor Progression NA BeFree Detail
<0.001 Carcinogenesis NA BeFree Detail
<0.001 stomach carcinoma NA BeFree Detail
0.120 hypogonadotropic hypogonadism 22 with or without anosmia NA UNIPROT Detail
0.002 autistic disorder NA GAD Detail
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
chr7:121,941,357-121,944,804
Variant Type
snv
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