chr12:102481086:A>G Detail (hg38) (IGF1)

Information

Genome

Assembly Position
hg19 chr12:102,874,864-102,874,864 View the variant detail on this assembly version.
hg38 chr12:102,481,086-102,481,086

HGVS

Type Transcript Protein
RefSeq
Ensemble ENST00000644491.1:c.-20+617T>C
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

JP HGVD:[No Data.]
ToMMo:0.303
NCBN:[No Data.]
NCBN(Hondo):[No Data.]
NCBN(Ryukyu):[No Data.]
East asia ExAC:[No Data.]

Prediction

ClinVar

Clinical Significance
Review star [No Data.]
Show details
Links
Type Database ID Link
Gene MIM 147440 OMIM
HGNC 5464 HGNC
Ensembl ENSG00000017427 Ensembl
NCBI NCBI
Gene Cards Gene Cards
OncoKB OncoKB
Type Database ID Link
Variant TogoVar tgv47031661 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 Polyp of large intestine We examined the risk of colorectal polyps in relation to body size factors and c... BeFree 20580999 Detail
<0.001 Polyp of large intestine We examined the risk of colorectal polyps in relation to body size factors and c... BeFree 20580999 Detail
<0.001 Adolescent idiopathic scoliosis This study revealed that the SNPs of rs2449539 in lysosomal-associated transmemb... BeFree 23364988 Detail
Annotation

Annotations

DescrptionSourceLinks
We examined the risk of colorectal polyps in relation to body size factors and candidate polymorphis... DisGeNET Detail
We examined the risk of colorectal polyps in relation to body size factors and candidate polymorphis... DisGeNET Detail
This study revealed that the SNPs of rs2449539 in lysosomal-associated transmembrane protein 4 beta ... DisGeNET Detail

Overlapped Transcript

Gene Transcript ID Chromosome Start Stop Links
Gene
-
dbSNP
rs5742612 dbSNP
Genome
hg38
Position
chr12:102,481,086-102,481,086
Variant Type
snv
Reference Allele
A
Alternative Allele
G
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))
rs5742612
Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
0.3035
Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
5086
Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
16760
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