chr10:14383222:G>C Detail (hg38) (FRMD4A)

Information

Genome

Assembly Position
hg19 chr10:14,425,221-14,425,221 View the variant detail on this assembly version.
hg38 chr10:14,383,222-14,383,222

HGVS

Type Transcript Protein
RefSeq
Ensemble ENST00000475141.2:c.-82+5459C>G
ENST00000493380.5:c.-81-53039C>G
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

JP HGVD:[No Data.]
ToMMo:0.097
NCBN:[No Data.]
NCBN(Hondo):[No Data.]
NCBN(Ryukyu):[No Data.]
East asia ExAC:0.076

Prediction

ClinVar

Clinical Significance
Review star [No Data.]
Show details
Links
Type Database ID Link
Gene MIM 616305 OMIM
HGNC 25491 HGNC
Ensembl ENSG00000151474 Ensembl
NCBI NCBI
Gene Cards Gene Cards
OncoKB OncoKB
Type Database ID Link
Variant TogoVar tgv38460292 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
<0.001 Nasopharyngeal carcinoma In this study, we analyzed associations between eight SNPs in miRNA mature seque... BeFree 25861865 Detail
<0.001 Nasopharyngeal carcinoma In this study, we analyzed associations between eight SNPs in miRNA mature seque... BeFree 25861865 Detail
<0.001 Nasopharyngeal carcinoma In this study, we analyzed associations between eight SNPs in miRNA mature seque... BeFree 25861865 Detail
<0.001 Nasopharyngeal carcinoma In this study, we analyzed associations between eight SNPs in miRNA mature seque... BeFree 25861865 Detail
<0.001 Nasopharyngeal carcinoma In this study, we analyzed associations between eight SNPs in miRNA mature seque... BeFree 25861865 Detail
<0.001 Nasopharyngeal carcinoma In this study, we analyzed associations between eight SNPs in miRNA mature seque... BeFree 25861865 Detail
<0.001 Nasopharyngeal carcinoma In this study, we analyzed associations between eight SNPs in miRNA mature seque... BeFree 25861865 Detail
Annotation

Annotations

DescrptionSourceLinks
In this study, we analyzed associations between eight SNPs in miRNA mature sequences (i.e., rs374644... DisGeNET Detail
In this study, we analyzed associations between eight SNPs in miRNA mature sequences (i.e., rs374644... DisGeNET Detail
In this study, we analyzed associations between eight SNPs in miRNA mature sequences (i.e., rs374644... DisGeNET Detail
In this study, we analyzed associations between eight SNPs in miRNA mature sequences (i.e., rs374644... DisGeNET Detail
In this study, we analyzed associations between eight SNPs in miRNA mature sequences (i.e., rs374644... DisGeNET Detail
In this study, we analyzed associations between eight SNPs in miRNA mature sequences (i.e., rs374644... DisGeNET Detail
In this study, we analyzed associations between eight SNPs in miRNA mature sequences (i.e., rs374644... 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
rs12220909 dbSNP
Genome
hg38
Position
chr10:14,383,222-14,383,222
Variant Type
snv
Reference Allele
G
Alternative Allele
C
ToMMo VCF FILTER column value (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
PASS
Total VCF ID column value (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
rs12220909
Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
0.0966
Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
1619
Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
16760
East Asian Chromosome Counts (ExAC)
66
East Asian Allele Counts (ExAC)
5
East Asian Heterozygous Counts (ExAC)
5
East Asian Homozygous Counts (ExAC)
0
East Asian Allele Frequency (ExAC)
0.07575757575757576
Chromosome Counts in All Race (ExAC)
1554
Allele Counts in All Race (ExAC)
15
Heterozygous Counts in All Race (ExAC)
13
Homozygous Counts in All Race (ExAC)
1
Allele Frequency in All Race (ExAC)
0.009652509652509652
Genome browser