| geneid | 51303 |
|---|---|
| ensemblid | ENSG00000134285.11 |
| hgncid | 18624 |
| symbol | FKBP11 |
| name | FKBP prolyl isomerase 11 |
| refseq_nuc | NM_016594.3 |
| refseq_prot | NP_057678.1 |
| ensembl_nuc | ENST00000550765.6 |
| ensembl_prot | ENSP00000449751.1 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 48921963 |
| end | 48925492 |
| strand | - |
| ver | v1.2 |
| region | chr12:48921963-48925492 |
| region5000 | chr12:48916963-48930492 |
| regionname0 | FKBP11_chr12_48921963_48925492 |
| regionname5000 | FKBP11_chr12_48916963_48930492 |
| chr:pos | ref | alt | af | annotation | impact | samples | AHAPIDS | ACHAPIDS | ACTHAPIDS | ACTGHAPIDS | ac | an | len | genename | geneid | featuretype | featureid | transcript_biotype | rank | hgvs_c | hgvs_p | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status |
|---|
| genename | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
ahapid | alen | total | AFR | AMR | EAS | EUR | SAS | aseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| FKBP11 | 1/1 | a0001 | 201 | 382 | 94 | 78 | 150 | 16 | 42 | subcellular location copy fasta | chr12 | 48916963 | 48930492 |
Click to load Haplotype QTL data...
| pos | S. Strand |
E# Exon Number |
max | median | min | diff | type | haplotypeid | max_hap_list | min_hap_list | symbol | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 48925300 | - | 1 | -0.7163 | -0.6801 | -0.6330 | 0.0833 | acceptor | a0001 | HG01109.hp1 HG02895.hp1 HG03041.hp1 HG03139.hp2 HG03209.hp2 others(1): Show |
HG01517.hp1 | FKBP11 | chr12 | 48916963 | 48930492 |
| 48925046 | - | 2 | -0.6181 | -0.5866 | -0.5482 | 0.0698 | acceptor | a0001 | NA18963.hp2 NA18966.hp1 NA18980.hp1 NA19007.hp2 |
NA18970.hp1 | FKBP11 | chr12 | 48916963 | 48930492 |
| 48925111 | - | 2 | 0.1469 | 0.1281 | 0.0862 | 0.0607 | donor | a0001 | HG01169.hp2 HG02976.hp2 |
NA18970.hp1 | FKBP11 | chr12 | 48916963 | 48930492 |
| 48924561 | - | 3 | -0.5940 | -0.5555 | -0.3686 | 0.2254 | acceptor | a0001 | HG01358.hp2 | NA18970.hp1 | FKBP11 | chr12 | 48916963 | 48930492 |
| 48924648 | - | 3 | 0.5505 | 0.5050 | 0.2964 | 0.2541 | donor | a0001 | HG01069.hp2 | NA18970.hp1 | FKBP11 | chr12 | 48916963 | 48930492 |
| 48924223 | - | 4 | -0.7619 | -0.7506 | -0.6744 | 0.0875 | acceptor | a0001 | HG02257.hp2 | NA18970.hp1 | FKBP11 | chr12 | 48916963 | 48930492 |
| 48924256 | - | 4 | 0.5930 | 0.5716 | 0.4754 | 0.1177 | donor | a0001 | HG03486.hp1 | NA18970.hp1 | FKBP11 | chr12 | 48916963 | 48930492 |
| 48923782 | - | 5 | -0.4250 | -0.3942 | -0.3471 | 0.0779 | acceptor | a0001 | NA21309.hp1 | NA18970.hp1 | FKBP11 | chr12 | 48916963 | 48930492 |
| 48923852 | - | 5 | 0.2236 | 0.2057 | 0.1485 | 0.0751 | donor | a0001 | HG01358.hp2 | NA18966.hp1 NA18980.hp1 NA18991.hp2 NA19007.hp2 |
FKBP11 | chr12 | 48916963 | 48930492 |
| 48922201 | - | 6 | 0.5282 | 0.4413 | 0.3897 | 0.1384 | donor | a0001 | HG01358.hp1 | NA18963.hp2 | FKBP11 | chr12 | 48916963 | 48930492 |
| pos | annotationhgvs_chgvs_p | clinvarid | clnsig | geneinfo | mc | clndisdb | strand strand
|
ahapid ahapid_count
|
chapid chapid count
|
thapid thapid_count
|
ghapid ghapid_count
|
AHAPIDS ahapids
|
ACHAPIDS achapids
|
ACTHAPIDS acthapids
|
ACTGHAPIDS actghapids
|
haplotypeids haplotypeids
|
impact | chr | ref | alt | external |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 48921097:splice 48921097:variant goto | c.*887T>A | 1235140 | Benign | DRC2:85478 | SO:0001627 intron_variant |
MONDO:MONDO:0014215 MedGen:C3809701 OMIM:615504 Orphanet:244|MedGen:C3661900 |
- | 1 | 1 | 1 | 1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | HG00323.hp2 HG02293.hp2 HG02735.hp1 HG03239.hp1 |
MODIFIER | chr12 | A | T | TogoVar |
| 48921160:splice 48921160:variant goto | c.*824T>G | 241744 | Benign/Likely_benign | DRC2:85478 | SO:0001627 intron_variant |
MedGen:C3661900|MONDO:MONDO:0014215 MedGen:C3809701 OMIM:615504 Orphanet:244 |
- | 1 | 1 | 1 | 1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | HG01109.hp2 | MODIFIER | chr12 | A | C | TogoVar |
| 48921312:splice 48921312:variant goto | c.*672C>T | 3707014 | Likely_benign | CCDC65:85478 | SO:0001583 missense_variant |
MONDO:MONDO:0014215 MedGen:C3809701 OMIM:615504 Orphanet:244 |
- | 1 | 1 | 1 | 1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | NA18964.hp1 | MODIFIER | chr12 | G | A | TogoVar |
| 48921517:splice 48921517:variant goto | c.*466dupA | 1243902 | Benign | CCDC65:85478 | SO:0001624 3_prime_UTR_variant |
MedGen:C3661900 | - | 1 | 1 | 2 | 14 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0002g0002others(9): Show | HG00423.hp2 HG00438.hp2 HG00558.hp1 HG00558.hp2 HG00609.hp1 others(116): Show |
MODIFIER | chr12 | A | AT | TogoVar |
| 48921134:splice 48921134:variant goto | c.*850C>G | 1251423 | Benign | DRC2:85478 | SO:0001627 intron_variant |
MedGen:C3661900 | - | 1 | 1 | 1 | 2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0003a0001c0001t0001g0011 | HG01358.hp2 HG03491.hp1 HG03669.hp1 HG04184.hp1 NA20300.hp2 others(2): Show |
MODIFIER | chr12 | G | C | TogoVar |
| 48917120:splice 48917120:variant goto | c.*4864C>T | 1570212 | Likely_benign | DRC2:85478 | SO:0001627 intron_variant |
MONDO:MONDO:0014215 MedGen:C3809701 OMIM:615504 Orphanet:244 |
- | 1 | 1 | 1 | 1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0004 | HG02965.hp2 | MODIFIER | chr12 | G | A | TogoVar |
| 48917268:splice 48917268:variant goto | c.*4716A>G | 1193853 | Likely_benign | DRC2:85478 | SO:0001627 intron_variant |
MedGen:C3661900 | - | 1 | 1 | 1 | 1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0004 | HG02451.hp2 HG02622.hp2 HG02717.hp1 HG02976.hp1 |
MODIFIER | chr12 | T | C | TogoVar |
| 48921037:splice 48921037:variant goto | c.*947C>T | 474634 | Benign/Likely_benign | DRC2:85478 | SO:0001819 synonymous_variant |
MedGen:C3661900|MONDO:MONDO:0014215 MedGen:C3809701 OMIM:615504 Orphanet:244 |
- | 1 | 1 | 1 | 1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0004 | HG02886.hp1 HG02965.hp2 HG03041.hp2 |
MODIFIER | chr12 | G | A | TogoVar |
| 48921403:splice 48921403:variant goto | c.*581C>T | 416602 | Benign | DRC2:85478 | SO:0001583 missense_variant |
MONDO:MONDO:0014215 MedGen:C3809701 OMIM:615504 Orphanet:244|MedGen:C3661900 |
- | 1 | 1 | 1 | 2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0005a0001c0001t0001g0012 | HG01346.hp2 HG01884.hp1 HG02572.hp1 HG02717.hp2 HG02922.hp2 others(6): Show |
MODIFIER | chr12 | G | A | TogoVar |
| 48917004:splice 48917004:variant goto | c.*4980G>T | 262220 | Benign | DRC2:85478 | SO:0001583 missense_variant |
MedGen:C3661900|MONDO:MONDO:0014215 MedGen:C3809701 OMIM:615504 Orphanet:244|MedGen:CN169374 |
- | 1 | 1 | 1 | 1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0007 | HG00733.hp1 HG00735.hp2 HG01081.hp1 HG01106.hp1 HG02615.hp1 others(1): Show |
MODIFIER | chr12 | C | A | TogoVar |
| 48918757:splice 48918757:variant goto | c.*3227G>A | 262221 | Benign | DRC2:85478 | SO:0001583 missense_variant |
MONDO:MONDO:0014215 MedGen:C3809701 OMIM:615504 Orphanet:244|MedGen:CN169374|MedGen:C3661900 |
- | 1 | 1 | 1 | 1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0007 | HG00733.hp1 HG00735.hp2 HG01081.hp1 HG01106.hp1 HG02615.hp1 others(1): Show |
MODIFIER | chr12 | C | T | TogoVar |
| 48917283:splice 48917283:variant goto | c.*4701T>C | 1275503 | Benign | DRC2:85478 | SO:0001627 intron_variant |
MedGen:C3661900 | - | 1 | 1 | 2 | 11 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0024a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0013a0001c0001t0002g0015others(6): Show | HG00099.hp2 HG00323.hp1 HG00423.hp2 HG00438.hp2 HG00558.hp1 others(122): Show |
MODIFIER | chr12 | A | G | TogoVar |
| 48917347:splice 48917347:variant goto | c.*4637G>A | 1272543 | Benign | DRC2:85478 | SO:0001627 intron_variant |
MedGen:C3661900 | - | 1 | 1 | 2 | 11 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0024a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0013a0001c0001t0002g0015others(6): Show | HG00099.hp2 HG00323.hp1 HG00423.hp2 HG00438.hp2 HG00558.hp1 others(122): Show |
MODIFIER | chr12 | C | T | TogoVar |
| 48917379:splice 48917379:variant goto | c.*4605C>T | 1287058 | Benign | DRC2:85478 | SO:0001627 intron_variant |
MedGen:C3661900 | - | 1 | 1 | 2 | 11 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0024a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0013a0001c0001t0002g0015others(6): Show | HG00099.hp2 HG00323.hp1 HG00423.hp2 HG00438.hp2 HG00558.hp1 others(122): Show |
MODIFIER | chr12 | G | A | TogoVar |
| 48917424:splice 48917424:variant goto | c.*4560T>C | 1224734 | Benign | DRC2:85478 | SO:0001627 intron_variant |
MedGen:C3661900 | - | 1 | 1 | 2 | 11 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0024a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0013a0001c0001t0002g0015others(6): Show | HG00099.hp2 HG00323.hp1 HG00423.hp2 HG00438.hp2 HG00558.hp1 others(122): Show |
MODIFIER | chr12 | A | G | TogoVar |
| 48918649:splice 48918649:variant goto | c.*3335G>A | 1243268 | Benign | DRC2:85478 | SO:0001627 intron_variant |
MedGen:C3661900 | - | 1 | 1 | 2 | 11 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0024a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0013a0001c0001t0002g0015others(6): Show | HG00099.hp2 HG00323.hp1 HG00423.hp2 HG00438.hp2 HG00558.hp1 others(122): Show |
MODIFIER | chr12 | C | T | TogoVar |
| 48919168:splice 48919168:variant goto | c.*2816G>A | 1278534 | Benign | CCDC65:85478 | SO:0001627 intron_variant |
MedGen:C3661900 | - | 1 | 1 | 2 | 11 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0024a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0013a0001c0001t0002g0015others(6): Show | HG00099.hp2 HG00323.hp1 HG00423.hp2 HG00438.hp2 HG00558.hp1 others(122): Show |
MODIFIER | chr12 | C | T | TogoVar |
| 48921079:splice 48921079:variant goto | c.*905G>T | 402503 | Benign | DRC2:85478 | SO:0001819 synonymous_variant |
MONDO:MONDO:0014215 MedGen:C3809701 OMIM:615504 Orphanet:244|MedGen:CN169374|MedGen:C3661900 |
- | 1 | 1 | 2 | 11 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0024a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0013a0001c0001t0002g0015others(6): Show | HG00099.hp2 HG00323.hp1 HG00423.hp2 HG00438.hp2 HG00558.hp1 others(122): Show |
MODIFIER | chr12 | C | A | TogoVar |
| 48921211:splice 48921211:variant goto | c.*773T>C | 402504 | Benign | DRC2:85478 | SO:0001583 missense_variant |
MONDO:MONDO:0014215 MedGen:C3809701 OMIM:615504 Orphanet:244|MedGen:CN169374|MedGen:C3661900 |
- | 1 | 1 | 2 | 11 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0024a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0013a0001c0001t0002g0015others(6): Show | HG00099.hp2 HG00323.hp1 HG00423.hp2 HG00438.hp2 HG00558.hp1 others(121): Show |
MODIFIER | chr12 | A | G | TogoVar |
| 48918810:splice 48918810:variant goto | c.*3174T>C | 402502 | Benign | DRC2:85478 | SO:0001819 synonymous_variant |
MedGen:C3661900|MONDO:MONDO:0014215 MedGen:C3809701 OMIM:615504 Orphanet:244|MedGen:CN169374 |
- | 1 | 1 | 2 | 10 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0024a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0013a0001c0001t0002g0015others(5): Show | HG00099.hp2 HG00323.hp1 HG00423.hp2 HG00438.hp2 HG00558.hp1 others(120): Show |
MODIFIER | chr12 | A | G | TogoVar |
| 48921330:splice 48921330:variant goto | c.*654C>T | 2420128 | Uncertain_significance | DRC2:85478 | SO:0001583 missense_variant |
MONDO:MONDO:0014215 MedGen:C3809701 OMIM:615504 Orphanet:244 |
- | 1 | 1 | 1 | 1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0027 | HG04204.hp1 | MODIFIER | chr12 | G | A | TogoVar |
| 48921417:splice 48921417:variant goto | c.*567C>T | 416601 | Benign/Likely_benign | DRC2:85478 | SO:0001583 missense_variant |
MONDO:MONDO:0014215 MedGen:C3809701 OMIM:615504 Orphanet:244|MedGen:C3661900 |
- | 1 | 1 | 1 | 1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0002 | HG00738.hp2 | MODIFIER | chr12 | G | A | TogoVar |
| 48921451:splice 48921451:variant goto | c.*533A>T | 3044818 | Benign | DRC2:85478 | SO:0001624 3_prime_UTR_variant |
. | - | 1 | 1 | 1 | 1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0002 | HG02451.hp1 HG02630.hp2 HG02922.hp1 |
MODIFIER | chr12 | T | A | TogoVar |
| 48921517:splice 48921517:variant goto | c.*465_*466dupAA | 1181703 | Benign | CCDC65:85478 | SO:0001624 3_prime_UTR_variant |
MedGen:C3661900 | - | 1 | 1 | 1 | 1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0002 | HG00099.hp2 HG00323.hp1 HG01074.hp1 HG01256.hp2 HG01258.hp2 others(3): Show |
MODIFIER | chr12 | A | ATT | TogoVar |
| 48918910:splice 48918910:variant goto | c.*3072_*3073delCT | 220953 | Benign | DRC2:85478 | SO:0001627 intron_variant |
MedGen:C3661900|MONDO:MONDO:0014215 MedGen:C3809701 OMIM:615504 Orphanet:244|MedGen:CN169374 |
- | 1 | 1 | 1 | 6 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0002a0001c0001t0002g0013a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0020others(1): Show | HG00558.hp2 HG00609.hp1 HG00621.hp1 HG00673.hp1 HG00733.hp2 others(49): Show |
MODIFIER | chr12 | CAG | C | TogoVar |
| CHR:POS | annotationhgvs_chgvs_p | disease trait-log10podds or beta | AHAPIDS ahapids
|
ACHAPIDS achapids
|
ACTHAPIDS acthapids
|
ACTGHAPIDS actghapids
|
haplotypeids haplotypeids
|
study | initial sample size/replication sample size | report genes | mapped gene | strongest snp risk allele | strand strand
|
impact | chr | ref | alt |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
chr12:48925253
|
c.129+47T>G | Heel bone mineral density0.0382365 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(21): Show | HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00280.hp1 others(344): Show |
Identification of 613 new loci associated with hee others(102): Show |
394,929 European ancestry individuals/ | CCDC65, FKBP11 | rs12829682-? | - | MODIFIER | chr12 | A | C |
| pos | genenamehgvs_chgvs_pannotation | tissueexpression gene-log10(pval)slope Tissue name in GTEx database(the target eQTL tissue name of the GTEx database)The -log10(nominal pvalue) in GTEx databaseSlope in GTEx database (positive value:alt allele has higher gene expression) |
ahapidchapidthapidghapid ahapid_countchapid_countthapid_countghapid_count
|
AHAPIDS ahapids
|
ACHAPIDS achapids
|
ACTHAPIDS acthapids
|
ACTGHAPIDS actghapids
|
haplotypeids haplotypeids
|
af allele frequency in GTEx database |
ms The number of samples with minor allele in GTEx database |
ma The number of minor allele count in GTEx database |
ver GTEx version |
vid Variant ID in GTEx database |
strand strand
|
impact | chr | ref | alt | external |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 48929743:splice 48929743:variant goto | FKBP11upstream_gene_variantc.-4315C>Gothers(2): Show | CCDC65 Adipose_Subcutaneous 6.005 0.316 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | HG01074.hp2 HG01099.hp2 HG01257.hp1 HG01258.hp1 HG02109.hp1 others(5): Show |
0.120 | 157 | 170 | 10 | chr12_48929743_G_C_b38 | - | MODIFIER | chr12 | G | C | TogoVar |
| 48929743:splice 48929743:variant goto | FKBP11upstream_gene_variantc.-4315C>Gothers(2): Show | CCDC65 Artery_Coronary 6.549 0.502 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | HG01074.hp2 HG01099.hp2 HG01257.hp1 HG01258.hp1 HG02109.hp1 others(5): Show |
0.110 | 55 | 59 | 10 | chr12_48929743_G_C_b38 | - | MODIFIER | chr12 | G | C | TogoVar |
| 48929743:splice 48929743:variant goto | FKBP11upstream_gene_variantc.-4315C>Gothers(2): Show | FKBP11 Artery_Tibial 6.150 0.159 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | HG01074.hp2 HG01099.hp2 HG01257.hp1 HG01258.hp1 HG02109.hp1 others(5): Show |
0.116 | 147 | 160 | 10 | chr12_48929743_G_C_b38 | - | MODIFIER | chr12 | G | C | TogoVar |
| 48929743:splice 48929743:variant goto | FKBP11upstream_gene_variantc.-4315C>Gothers(2): Show | WNT10B Brain_Amygdala 4.280 0.260 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | HG01074.hp2 HG01099.hp2 HG01257.hp1 HG01258.hp1 HG02109.hp1 others(5): Show |
0.106 | 33 | 38 | 10 | chr12_48929743_G_C_b38 | - | MODIFIER | chr12 | G | C | TogoVar |
| 48929743:splice 48929743:variant goto | FKBP11upstream_gene_variantc.-4315C>Gothers(2): Show | WNT10B Brain_Anterior_cingulate_cortex_BA24 4.523 0.265 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | HG01074.hp2 HG01099.hp2 HG01257.hp1 HG01258.hp1 HG02109.hp1 others(5): Show |
0.129 | 54 | 60 | 10 | chr12_48929743_G_C_b38 | - | MODIFIER | chr12 | G | C | TogoVar |
| 48929743:splice 48929743:variant goto | FKBP11upstream_gene_variantc.-4315C>Gothers(2): Show | CCDC65 Brain_Cerebellar_Hemisphere 4.073 0.433 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | HG01074.hp2 HG01099.hp2 HG01257.hp1 HG01258.hp1 HG02109.hp1 others(5): Show |
0.120 | 59 | 66 | 10 | chr12_48929743_G_C_b38 | - | MODIFIER | chr12 | G | C | TogoVar |
| 48929743:splice 48929743:variant goto | FKBP11upstream_gene_variantc.-4315C>Gothers(2): Show | FKBP11 Brain_Cerebellar_Hemisphere 3.739 0.267 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | HG01074.hp2 HG01099.hp2 HG01257.hp1 HG01258.hp1 HG02109.hp1 others(5): Show |
0.120 | 59 | 66 | 10 | chr12_48929743_G_C_b38 | - | MODIFIER | chr12 | G | C | TogoVar |
| 48929743:splice 48929743:variant goto | FKBP11upstream_gene_variantc.-4315C>Gothers(2): Show | CCDC65 Brain_Cerebellum 7.353 0.665 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | HG01074.hp2 HG01099.hp2 HG01257.hp1 HG01258.hp1 HG02109.hp1 others(5): Show |
0.112 | 53 | 59 | 10 | chr12_48929743_G_C_b38 | - | MODIFIER | chr12 | G | C | TogoVar |
| 48929743:splice 48929743:variant goto | FKBP11upstream_gene_variantc.-4315C>Gothers(2): Show | WNT10B Brain_Cortex 5.197 0.239 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | HG01074.hp2 HG01099.hp2 HG01257.hp1 HG01258.hp1 HG02109.hp1 others(5): Show |
0.123 | 60 | 66 | 10 | chr12_48929743_G_C_b38 | - | MODIFIER | chr12 | G | C | TogoVar |
| 48929743:splice 48929743:variant goto | FKBP11upstream_gene_variantc.-4315C>Gothers(2): Show | FKBP11 Brain_Frontal_Cortex_BA9 3.857 0.276 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | HG01074.hp2 HG01099.hp2 HG01257.hp1 HG01258.hp1 HG02109.hp1 others(5): Show |
0.121 | 59 | 65 | 10 | chr12_48929743_G_C_b38 | - | MODIFIER | chr12 | G | C | TogoVar |
| 48929743:splice 48929743:variant goto | FKBP11upstream_gene_variantc.-4315C>Gothers(2): Show | WNT10B Brain_Frontal_Cortex_BA9 5.073 0.244 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | HG01074.hp2 HG01099.hp2 HG01257.hp1 HG01258.hp1 HG02109.hp1 others(5): Show |
0.121 | 59 | 65 | 10 | chr12_48929743_G_C_b38 | - | MODIFIER | chr12 | G | C | TogoVar |
| 48929743:splice 48929743:variant goto | FKBP11upstream_gene_variantc.-4315C>Gothers(2): Show | CCDC65 Breast_Mammary_Tissue 5.462 0.333 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | HG01074.hp2 HG01099.hp2 HG01257.hp1 HG01258.hp1 HG02109.hp1 others(5): Show |
0.128 | 121 | 131 | 10 | chr12_48929743_G_C_b38 | - | MODIFIER | chr12 | G | C | TogoVar |
| 48929743:splice 48929743:variant goto | FKBP11upstream_gene_variantc.-4315C>Gothers(2): Show | CCDC65 Cells_Cultured_fibroblasts 4.970 0.281 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | HG01074.hp2 HG01099.hp2 HG01257.hp1 HG01258.hp1 HG02109.hp1 others(5): Show |
0.114 | 140 | 148 | 10 | chr12_48929743_G_C_b38 | - | MODIFIER | chr12 | G | C | TogoVar |
| 48929743:splice 48929743:variant goto | FKBP11upstream_gene_variantc.-4315C>Gothers(2): Show | FKBP11 Cells_Cultured_fibroblasts 5.266 0.135 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | HG01074.hp2 HG01099.hp2 HG01257.hp1 HG01258.hp1 HG02109.hp1 others(5): Show |
0.114 | 140 | 148 | 10 | chr12_48929743_G_C_b38 | - | MODIFIER | chr12 | G | C | TogoVar |
| 48929743:splice 48929743:variant goto | FKBP11upstream_gene_variantc.-4315C>Gothers(2): Show | ARF3 Cells_Cultured_fibroblasts 4.105 -0.114 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | HG01074.hp2 HG01099.hp2 HG01257.hp1 HG01258.hp1 HG02109.hp1 others(5): Show |
0.114 | 140 | 148 | 10 | chr12_48929743_G_C_b38 | - | MODIFIER | chr12 | G | C | TogoVar |
| 48927946:splice 48927946:variant goto | FKBP11upstream_gene_variantc.-2518A>Gothers(2): Show | DNAJC22 Cells_Cultured_fibroblasts 3.772 -0.315 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | HG00280.hp2 HG01070.hp1 HG01123.hp2 |
0.016 | 20 | 21 | 10 | chr12_48927946_T_C_b38 | - | MODIFIER | chr12 | T | C | TogoVar |
| 48929743:splice 48929743:variant goto | FKBP11upstream_gene_variantc.-4315C>Gothers(2): Show | CCDC65 Esophagus_Gastroesophageal_Junction 4.745 0.327 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | HG01074.hp2 HG01099.hp2 HG01257.hp1 HG01258.hp1 HG02109.hp1 others(5): Show |
0.124 | 91 | 100 | 10 | chr12_48929743_G_C_b38 | - | MODIFIER | chr12 | G | C | TogoVar |
| 48929743:splice 48929743:variant goto | FKBP11upstream_gene_variantc.-4315C>Gothers(2): Show | CCDC65 Esophagus_Muscularis 7.712 0.340 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | HG01074.hp2 HG01099.hp2 HG01257.hp1 HG01258.hp1 HG02109.hp1 others(5): Show |
0.120 | 123 | 135 | 10 | chr12_48929743_G_C_b38 | - | MODIFIER | chr12 | G | C | TogoVar |
| 48927946:splice 48927946:variant goto | FKBP11upstream_gene_variantc.-2518A>Gothers(2): Show | DNAJC22 Minor_Salivary_Gland 6.621 -1.167 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | HG00280.hp2 HG01070.hp1 HG01123.hp2 |
0.011 | 3 | 4 | 10 | chr12_48927946_T_C_b38 | - | MODIFIER | chr12 | T | C | TogoVar |
| 48929743:splice 48929743:variant goto | FKBP11upstream_gene_variantc.-4315C>Gothers(2): Show | CCDC65 Nerve_Tibial 8.060 0.356 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | HG01074.hp2 HG01099.hp2 HG01257.hp1 HG01258.hp1 HG02109.hp1 others(5): Show |
0.124 | 153 | 166 | 10 | chr12_48929743_G_C_b38 | - | MODIFIER | chr12 | G | C | TogoVar |
| 48929743:splice 48929743:variant goto | FKBP11upstream_gene_variantc.-4315C>Gothers(2): Show | FKBP11 Nerve_Tibial 4.991 0.157 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | HG01074.hp2 HG01099.hp2 HG01257.hp1 HG01258.hp1 HG02109.hp1 others(5): Show |
0.124 | 153 | 166 | 10 | chr12_48929743_G_C_b38 | - | MODIFIER | chr12 | G | C | TogoVar |
| 48929743:splice 48929743:variant goto | FKBP11upstream_gene_variantc.-4315C>Gothers(2): Show | CCDC65 Pancreas 5.606 0.368 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | HG01074.hp2 HG01099.hp2 HG01257.hp1 HG01258.hp1 HG02109.hp1 others(5): Show |
0.126 | 82 | 91 | 10 | chr12_48929743_G_C_b38 | - | MODIFIER | chr12 | G | C | TogoVar |
| 48929743:splice 48929743:variant goto | FKBP11upstream_gene_variantc.-4315C>Gothers(2): Show | CCDC65 Pituitary 5.206 0.372 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | HG01074.hp2 HG01099.hp2 HG01257.hp1 HG01258.hp1 HG02109.hp1 others(5): Show |
0.117 | 69 | 73 | 10 | chr12_48929743_G_C_b38 | - | MODIFIER | chr12 | G | C | TogoVar |
| 48921097:splice 48921097:variant goto | FKBP11downstream_gene_variantc.*887T>A others(3): Show |
C1QL4 Prostate 4.182 0.744 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | HG00323.hp2 HG02293.hp2 HG02735.hp1 HG03239.hp1 |
0.041 | 23 | 23 | 10 | chr12_48921097_A_T_b38 | - | MODIFIER | chr12 | A | T | TogoVar |
| 48929743:splice 48929743:variant goto | FKBP11upstream_gene_variantc.-4315C>Gothers(2): Show | CCDC65 Skin_Not_Sun_Exposed_Suprapubic 4.623 0.269 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | HG01074.hp2 HG01099.hp2 HG01257.hp1 HG01258.hp1 HG02109.hp1 others(5): Show |
0.114 | 139 | 148 | 10 | chr12_48929743_G_C_b38 | - | MODIFIER | chr12 | G | C | TogoVar |
| 48929743:splice 48929743:variant goto | FKBP11upstream_gene_variantc.-4315C>Gothers(2): Show | FKBP11 Testis 4.583 0.296 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | HG01074.hp2 HG01099.hp2 HG01257.hp1 HG01258.hp1 HG02109.hp1 others(5): Show |
0.105 | 79 | 87 | 10 | chr12_48929743_G_C_b38 | - | MODIFIER | chr12 | G | C | TogoVar |
| 48921097:splice 48921097:variant goto | FKBP11downstream_gene_variantc.*887T>A others(3): Show |
C1QL4 Thyroid 3.635 0.481 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | HG00323.hp2 HG02293.hp2 HG02735.hp1 HG03239.hp1 |
0.029 | 39 | 39 | 10 | chr12_48921097_A_T_b38 | - | MODIFIER | chr12 | A | T | TogoVar |
| 48927946:splice 48927946:variant goto | FKBP11upstream_gene_variantc.-2518A>Gothers(2): Show | DNAJC22 Thyroid 5.819 -0.485 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | HG00280.hp2 HG01070.hp1 HG01123.hp2 |
0.016 | 20 | 22 | 10 | chr12_48927946_T_C_b38 | - | MODIFIER | chr12 | T | C | TogoVar |
| 48929743:splice 48929743:variant goto | FKBP11upstream_gene_variantc.-4315C>Gothers(2): Show | CCDC65 Uterus 5.691 0.714 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | HG01074.hp2 HG01099.hp2 HG01257.hp1 HG01258.hp1 HG02109.hp1 others(5): Show |
0.118 | 35 | 36 | 10 | chr12_48929743_G_C_b38 | - | MODIFIER | chr12 | G | C | TogoVar |
| 48927735:splice 48927735:variant goto | FKBP11upstream_gene_variantc.-2307G>Aothers(2): Show | WNT10B Brain_Caudate_basal_ganglia 3.914 -0.259 | 11227 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(22): Show | HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00280.hp1 others(348): Show |
0.950 | 25 | 30 | 10 | chr12_48927735_C_T_b38 | - | MODIFIER | chr12 | C | T | TogoVar |
| 48927735:splice 48927735:variant goto | FKBP11upstream_gene_variantc.-2307G>Aothers(2): Show | WNT10B Esophagus_Mucosa 4.616 -0.379 | 11227 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(22): Show | HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00280.hp1 others(348): Show |
0.944 | 62 | 69 | 10 | chr12_48927735_C_T_b38 | - | MODIFIER | chr12 | C | T | TogoVar |
| 48927735:splice 48927735:variant goto | FKBP11upstream_gene_variantc.-2307G>Aothers(2): Show | FKBP11 Nerve_Tibial 4.337 -0.213 | 11227 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(22): Show | HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00280.hp1 others(348): Show |
0.941 | 69 | 79 | 10 | chr12_48927735_C_T_b38 | - | MODIFIER | chr12 | C | T | TogoVar |
| 48927735:splice 48927735:variant goto | FKBP11upstream_gene_variantc.-2307G>Aothers(2): Show | ARF3 Whole_Blood 6.189 0.150 | 11227 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(22): Show | HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00280.hp1 others(348): Show |
0.941 | 84 | 94 | 10 | chr12_48927735_C_T_b38 | - | MODIFIER | chr12 | C | T | TogoVar |
| 48925253:splice 48925253:variant goto | FKBP11intron_variantc.129+47T>G | WNT10B Brain_Caudate_basal_ganglia 4.055 -0.259 | 11226 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(21): Show | HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00280.hp1 others(344): Show |
0.946 | 26 | 32 | 10 | chr12_48925253_A_C_b38 | - | MODIFIER | chr12 | A | C | TogoVar |
| 48925253:splice 48925253:variant goto | FKBP11intron_variantc.129+47T>G | WNT10B Esophagus_Mucosa 4.491 -0.369 | 11226 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(21): Show | HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00280.hp1 others(344): Show |
0.941 | 64 | 72 | 10 | chr12_48925253_A_C_b38 | - | MODIFIER | chr12 | A | C | TogoVar |
| 48925253:splice 48925253:variant goto | FKBP11intron_variantc.129+47T>G | FKBP11 Nerve_Tibial 4.448 -0.209 | 11226 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(21): Show | HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00280.hp1 others(344): Show |
0.937 | 71 | 84 | 10 | chr12_48925253_A_C_b38 | - | MODIFIER | chr12 | A | C | TogoVar |
| 48925253:splice 48925253:variant goto | FKBP11intron_variantc.129+47T>G | C1QL4 Testis 3.901 0.350 | 11226 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(21): Show | HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00280.hp1 others(344): Show |
0.935 | 48 | 54 | 10 | chr12_48925253_A_C_b38 | - | MODIFIER | chr12 | A | C | TogoVar |
| 48925253:splice 48925253:variant goto | FKBP11intron_variantc.129+47T>G | ARF3 Whole_Blood 5.868 0.142 | 11226 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(21): Show | HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00280.hp1 others(344): Show |
0.938 | 87 | 100 | 10 | chr12_48925253_A_C_b38 | - | MODIFIER | chr12 | A | C | TogoVar |
| 48919396:splice 48919396:variant goto | FKBP11downstream_gene_variantc.*2588C>T< others(4): Show |
KANSL2 Adipose_Subcutaneous 3.878 0.257 | 1122 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0001a0001c0001t0002g0002 | HG00099.hp2 HG00323.hp1 HG00673.hp2 HG01074.hp1 HG01256.hp2 others(2): Show |
0.060 | 85 | 86 | 10 | chr12_48919396_G_A_b38 | - | MODIFIER | chr12 | G | A | TogoVar |
| 48919396:splice 48919396:variant goto | FKBP11downstream_gene_variantc.*2588C>T< others(4): Show |
CCDC65 Brain_Cerebellum 3.916 -0.645 | 1122 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0001a0001c0001t0002g0002 | HG00099.hp2 HG00323.hp1 HG00673.hp2 HG01074.hp1 HG01256.hp2 others(2): Show |
0.070 | 36 | 37 | 10 | chr12_48919396_G_A_b38 | - | MODIFIER | chr12 | G | A | TogoVar |
| 48919396:splice 48919396:variant goto | FKBP11downstream_gene_variantc.*2588C>T< others(4): Show |
ARF3 Cells_Cultured_fibroblasts 6.285 0.185 | 1122 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0001a0001c0001t0002g0002 | HG00099.hp2 HG00323.hp1 HG00673.hp2 HG01074.hp1 HG01256.hp2 others(2): Show |
0.062 | 78 | 81 | 10 | chr12_48919396_G_A_b38 | - | MODIFIER | chr12 | G | A | TogoVar |
| 48919396:splice 48919396:variant goto | FKBP11downstream_gene_variantc.*2588C>T< others(4): Show |
KANSL2 Lung 5.831 0.399 | 1122 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0001a0001c0001t0002g0002 | HG00099.hp2 HG00323.hp1 HG00673.hp2 HG01074.hp1 HG01256.hp2 others(2): Show |
0.063 | 75 | 76 | 10 | chr12_48919396_G_A_b38 | - | MODIFIER | chr12 | G | A | TogoVar |
| 48919396:splice 48919396:variant goto | FKBP11downstream_gene_variantc.*2588C>T< others(4): Show |
DDN Muscle_Skeletal 4.096 0.248 | 1122 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0001a0001c0001t0002g0002 | HG00099.hp2 HG00323.hp1 HG00673.hp2 HG01074.hp1 HG01256.hp2 others(2): Show |
0.060 | 96 | 98 | 10 | chr12_48919396_G_A_b38 | - | MODIFIER | chr12 | G | A | TogoVar |
| 48919396:splice 48919396:variant goto | FKBP11downstream_gene_variantc.*2588C>T< others(4): Show |
KANSL2 Nerve_Tibial 3.842 0.258 | 1122 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0001a0001c0001t0002g0002 | HG00099.hp2 HG00323.hp1 HG00673.hp2 HG01074.hp1 HG01256.hp2 others(2): Show |
0.059 | 76 | 79 | 10 | chr12_48919396_G_A_b38 | - | MODIFIER | chr12 | G | A | TogoVar |
| 48919396:splice 48919396:variant goto | FKBP11downstream_gene_variantc.*2588C>T< others(4): Show |
CCDC65 Skin_Not_Sun_Exposed_Suprapubic 4.144 -0.340 | 1122 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0001a0001c0001t0002g0002 | HG00099.hp2 HG00323.hp1 HG00673.hp2 HG01074.hp1 HG01256.hp2 others(2): Show |
0.062 | 79 | 81 | 10 | chr12_48919396_G_A_b38 | - | MODIFIER | chr12 | G | A | TogoVar |
| 48919396:splice 48919396:variant goto | FKBP11downstream_gene_variantc.*2588C>T< others(4): Show |
CCDC65 Testis 6.269 -0.183 | 1122 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0001a0001c0001t0002g0002 | HG00099.hp2 HG00323.hp1 HG00673.hp2 HG01074.hp1 HG01256.hp2 others(2): Show |
0.062 | 50 | 51 | 10 | chr12_48919396_G_A_b38 | - | MODIFIER | chr12 | G | A | TogoVar |
| 48919396:splice 48919396:variant goto | FKBP11downstream_gene_variantc.*2588C>T< others(4): Show |
KANSL2 Thyroid 3.895 0.236 | 1122 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0001a0001c0001t0002g0002 | HG00099.hp2 HG00323.hp1 HG00673.hp2 HG01074.hp1 HG01256.hp2 others(2): Show |
0.070 | 92 | 95 | 10 | chr12_48919396_G_A_b38 | - | MODIFIER | chr12 | G | A | TogoVar |
| 48921134:splice 48921134:variant goto | FKBP11downstream_gene_variantc.*850C>G others(3): Show |
SPATS2 Muscle_Skeletal 4.112 0.265 | 1112 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0003a0001c0001t0001g0011 | HG01358.hp2 HG03491.hp1 HG03669.hp1 HG04184.hp1 NA20300.hp2 others(2): Show |
0.037 | 60 | 61 | 10 | chr12_48921134_G_C_b38 | - | MODIFIER | chr12 | G | C | TogoVar |
| 48924763:splice 48924763:variant goto | FKBP11intron_variantc.196-115C>T | CACNB3 Adipose_Subcutaneous 3.916 -0.090 | 11215 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0027others(10): Show | HG00099.hp2 HG00323.hp1 HG00423.hp2 HG00438.hp2 HG00558.hp1 others(164): Show |
0.436 | 491 | 620 | 10 | chr12_48924763_G_A_b38 | - | MODIFIER | chr12 | G | A | TogoVar |
| 48924763:splice 48924763:variant goto | FKBP11intron_variantc.196-115C>T | CCDC65 Adipose_Subcutaneous 23.283 -0.435 | 11215 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0027others(10): Show | HG00099.hp2 HG00323.hp1 HG00423.hp2 HG00438.hp2 HG00558.hp1 others(164): Show |
0.436 | 491 | 620 | 10 | chr12_48924763_G_A_b38 | - | MODIFIER | chr12 | G | A | TogoVar |
| 48924763:splice 48924763:variant goto | FKBP11intron_variantc.196-115C>T | FKBP11 Adipose_Subcutaneous 13.860 -0.206 | 11215 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0027others(10): Show | HG00099.hp2 HG00323.hp1 HG00423.hp2 HG00438.hp2 HG00558.hp1 others(164): Show |
0.436 | 491 | 620 | 10 | chr12_48924763_G_A_b38 | - | MODIFIER | chr12 | G | A | TogoVar |
| 48924763:splice 48924763:variant goto | FKBP11intron_variantc.196-115C>T | ARF3 Adipose_Subcutaneous 4.216 0.101 | 11215 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0027others(10): Show | HG00099.hp2 HG00323.hp1 HG00423.hp2 HG00438.hp2 HG00558.hp1 others(164): Show |
0.436 | 491 | 620 | 10 | chr12_48924763_G_A_b38 | - | MODIFIER | chr12 | G | A | TogoVar |
| 48924763:splice 48924763:variant goto | FKBP11intron_variantc.196-115C>T | CCDC65 Adipose_Visceral_Omentum 20.862 -0.367 | 11215 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0027others(10): Show | HG00099.hp2 HG00323.hp1 HG00423.hp2 HG00438.hp2 HG00558.hp1 others(164): Show |
0.432 | 395 | 505 | 10 | chr12_48924763_G_A_b38 | - | MODIFIER | chr12 | G | A | TogoVar |
| 48924763:splice 48924763:variant goto | FKBP11intron_variantc.196-115C>T | FKBP11 Adipose_Visceral_Omentum 10.249 -0.149 | 11215 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0027others(10): Show | HG00099.hp2 HG00323.hp1 HG00423.hp2 HG00438.hp2 HG00558.hp1 others(164): Show |
0.432 | 395 | 505 | 10 | chr12_48924763_G_A_b38 | - | MODIFIER | chr12 | G | A | TogoVar |
| 48924763:splice 48924763:variant goto | FKBP11intron_variantc.196-115C>T | ARF3 Adipose_Visceral_Omentum 7.186 0.114 | 11215 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0027others(10): Show | HG00099.hp2 HG00323.hp1 HG00423.hp2 HG00438.hp2 HG00558.hp1 others(164): Show |
0.432 | 395 | 505 | 10 | chr12_48924763_G_A_b38 | - | MODIFIER | chr12 | G | A | TogoVar |
| 48924763:splice 48924763:variant goto | FKBP11intron_variantc.196-115C>T | CCDC65 Adrenal_Gland 6.606 -0.324 | 11215 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0027others(10): Show | HG00099.hp2 HG00323.hp1 HG00423.hp2 HG00438.hp2 HG00558.hp1 others(164): Show |
0.432 | 204 | 255 | 10 | chr12_48924763_G_A_b38 | - | MODIFIER | chr12 | G | A | TogoVar |
| 48924763:splice 48924763:variant goto | FKBP11intron_variantc.196-115C>T | ARF3 Adrenal_Gland 7.439 0.147 | 11215 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0027others(10): Show | HG00099.hp2 HG00323.hp1 HG00423.hp2 HG00438.hp2 HG00558.hp1 others(164): Show |
0.432 | 204 | 255 | 10 | chr12_48924763_G_A_b38 | - | MODIFIER | chr12 | G | A | TogoVar |
| 48924763:splice 48924763:variant goto | FKBP11intron_variantc.196-115C>T | CCDC65 Artery_Aorta 14.303 -0.398 | 11215 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0027others(10): Show | HG00099.hp2 HG00323.hp1 HG00423.hp2 HG00438.hp2 HG00558.hp1 others(164): Show |
0.432 | 329 | 408 | 10 | chr12_48924763_G_A_b38 | - | MODIFIER | chr12 | G | A | TogoVar |
| 48924763:splice 48924763:variant goto | FKBP11intron_variantc.196-115C>T | FKBP11 Artery_Aorta 9.936 -0.190 | 11215 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0027others(10): Show | HG00099.hp2 HG00323.hp1 HG00423.hp2 HG00438.hp2 HG00558.hp1 others(164): Show |
0.432 | 329 | 408 | 10 | chr12_48924763_G_A_b38 | - | MODIFIER | chr12 | G | A | TogoVar |
| 48924763:splice 48924763:variant goto | FKBP11intron_variantc.196-115C>T | CCDC65 Artery_Coronary 13.744 -0.453 | 11215 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0027others(10): Show | HG00099.hp2 HG00323.hp1 HG00423.hp2 HG00438.hp2 HG00558.hp1 others(164): Show |
0.444 | 185 | 238 | 10 | chr12_48924763_G_A_b38 | - | MODIFIER | chr12 | G | A | TogoVar |
| 48924763:splice 48924763:variant goto | FKBP11intron_variantc.196-115C>T | FKBP11 Artery_Coronary 5.689 -0.154 | 11215 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0027others(10): Show | HG00099.hp2 HG00323.hp1 HG00423.hp2 HG00438.hp2 HG00558.hp1 others(164): Show |
0.444 | 185 | 238 | 10 | chr12_48924763_G_A_b38 | - | MODIFIER | chr12 | G | A | TogoVar |
| 48924763:splice 48924763:variant goto | FKBP11intron_variantc.196-115C>T | CCDC65 Artery_Tibial 28.666 -0.412 | 11215 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0027others(10): Show | HG00099.hp2 HG00323.hp1 HG00423.hp2 HG00438.hp2 HG00558.hp1 others(164): Show |
0.451 | 482 | 622 | 10 | chr12_48924763_G_A_b38 | - | MODIFIER | chr12 | G | A | TogoVar |
| 48924763:splice 48924763:variant goto | FKBP11intron_variantc.196-115C>T | FKBP11 Artery_Tibial 14.624 -0.165 | 11215 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0027others(10): Show | HG00099.hp2 HG00323.hp1 HG00423.hp2 HG00438.hp2 HG00558.hp1 others(164): Show |
0.451 | 482 | 622 | 10 | chr12_48924763_G_A_b38 | - | MODIFIER | chr12 | G | A | TogoVar |
| 48924763:splice 48924763:variant goto | FKBP11intron_variantc.196-115C>T | FKBP11 Brain_Amygdala 6.667 -0.342 | 11215 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0027others(10): Show | HG00099.hp2 HG00323.hp1 HG00423.hp2 HG00438.hp2 HG00558.hp1 others(164): Show |
0.428 | 122 | 154 | 10 | chr12_48924763_G_A_b38 | - | MODIFIER | chr12 | G | A | TogoVar |
| 48924763:splice 48924763:variant goto | FKBP11intron_variantc.196-115C>T | WNT10B Brain_Amygdala 13.533 -0.333 | 11215 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0027others(10): Show | HG00099.hp2 HG00323.hp1 HG00423.hp2 HG00438.hp2 HG00558.hp1 others(164): Show |
0.428 | 122 | 154 | 10 | chr12_48924763_G_A_b38 | - | MODIFIER | chr12 | G | A | TogoVar |
| 48924763:splice 48924763:variant goto | FKBP11intron_variantc.196-115C>T | CCDC65 Brain_Anterior_cingulate_cortex_BA24 7.231 -0.308 | 11215 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0027others(10): Show | HG00099.hp2 HG00323.hp1 HG00423.hp2 HG00438.hp2 HG00558.hp1 others(164): Show |
0.425 | 154 | 198 | 10 | chr12_48924763_G_A_b38 | - | MODIFIER | chr12 | G | A | TogoVar |
| 48924763:splice 48924763:variant goto | FKBP11intron_variantc.196-115C>T | FKBP11 Brain_Anterior_cingulate_cortex_BA24 9.746 -0.341 | 11215 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0027others(10): Show | HG00099.hp2 HG00323.hp1 HG00423.hp2 HG00438.hp2 HG00558.hp1 others(164): Show |
0.425 | 154 | 198 | 10 | chr12_48924763_G_A_b38 | - | MODIFIER | chr12 | G | A | TogoVar |
| 48924763:splice 48924763:variant goto | FKBP11intron_variantc.196-115C>T | WNT10B Brain_Anterior_cingulate_cortex_BA24 12.412 -0.318 | 11215 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0027others(10): Show | HG00099.hp2 HG00323.hp1 HG00423.hp2 HG00438.hp2 HG00558.hp1 others(164): Show |
0.425 | 154 | 198 | 10 | chr12_48924763_G_A_b38 | - | MODIFIER | chr12 | G | A | TogoVar |
| 48924763:splice 48924763:variant goto | FKBP11intron_variantc.196-115C>T | CCDC65 Brain_Caudate_basal_ganglia 6.204 -0.157 | 11215 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0027others(10): Show | HG00099.hp2 HG00323.hp1 HG00423.hp2 HG00438.hp2 HG00558.hp1 others(164): Show |
0.435 | 201 | 259 | 10 | chr12_48924763_G_A_b38 | - | MODIFIER | chr12 | G | A | TogoVar |
| 48924763:splice 48924763:variant goto | FKBP11intron_variantc.196-115C>T | FKBP11 Brain_Caudate_basal_ganglia 15.527 -0.322 | 11215 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0027others(10): Show | HG00099.hp2 HG00323.hp1 HG00423.hp2 HG00438.hp2 HG00558.hp1 others(164): Show |
0.435 | 201 | 259 | 10 | chr12_48924763_G_A_b38 | - | MODIFIER | chr12 | G | A | TogoVar |
| 48924763:splice 48924763:variant goto | FKBP11intron_variantc.196-115C>T | CCDC65 Brain_Cerebellar_Hemisphere 30.180 -0.776 | 11215 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0027others(10): Show | HG00099.hp2 HG00323.hp1 HG00423.hp2 HG00438.hp2 HG00558.hp1 others(164): Show |
0.438 | 189 | 242 | 10 | chr12_48924763_G_A_b38 | - | MODIFIER | chr12 | G | A | TogoVar |
| 48924763:splice 48924763:variant goto | FKBP11intron_variantc.196-115C>T | FKBP11 Brain_Cerebellar_Hemisphere 19.254 -0.418 | 11215 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0027others(10): Show | HG00099.hp2 HG00323.hp1 HG00423.hp2 HG00438.hp2 HG00558.hp1 others(164): Show |
0.438 | 189 | 242 | 10 | chr12_48924763_G_A_b38 | - | MODIFIER | chr12 | G | A | TogoVar |
| 48924763:splice 48924763:variant goto | FKBP11intron_variantc.196-115C>T | CCDC65 Brain_Cerebellum 39.238 -0.992 | 11215 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0027others(10): Show | HG00099.hp2 HG00323.hp1 HG00423.hp2 HG00438.hp2 HG00558.hp1 others(164): Show |
0.439 | 183 | 232 | 10 | chr12_48924763_G_A_b38 | - | MODIFIER | chr12 | G | A | TogoVar |
| 48924763:splice 48924763:variant goto | FKBP11intron_variantc.196-115C>T | FKBP11 Brain_Cerebellum 22.710 -0.571 | 11215 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0027others(10): Show | HG00099.hp2 HG00323.hp1 HG00423.hp2 HG00438.hp2 HG00558.hp1 others(164): Show |
0.439 | 183 | 232 | 10 | chr12_48924763_G_A_b38 | - | MODIFIER | chr12 | G | A | TogoVar |
| 48924763:splice 48924763:variant goto | FKBP11intron_variantc.196-115C>T | CCDC65 Brain_Cortex 20.711 -0.471 | 11215 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0027others(10): Show | HG00099.hp2 HG00323.hp1 HG00423.hp2 HG00438.hp2 HG00558.hp1 others(164): Show |
0.453 | 191 | 243 | 10 | chr12_48924763_G_A_b38 | - | MODIFIER | chr12 | G | A | TogoVar |
| 48924763:splice 48924763:variant goto | FKBP11intron_variantc.196-115C>T | FKBP11 Brain_Cortex 10.497 -0.349 | 11215 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0027others(10): Show | HG00099.hp2 HG00323.hp1 HG00423.hp2 HG00438.hp2 HG00558.hp1 others(164): Show |
0.453 | 191 | 243 | 10 | chr12_48924763_G_A_b38 | - | MODIFIER | chr12 | G | A | TogoVar |
| 48924763:splice 48924763:variant goto | FKBP11intron_variantc.196-115C>T | WNT10B Brain_Cortex 11.662 -0.252 | 11215 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0027others(10): Show | HG00099.hp2 HG00323.hp1 HG00423.hp2 HG00438.hp2 HG00558.hp1 others(164): Show |
0.453 | 191 | 243 | 10 | chr12_48924763_G_A_b38 | - | MODIFIER | chr12 | G | A | TogoVar |
| 48924763:splice 48924763:variant goto | FKBP11intron_variantc.196-115C>T | CCDC65 Brain_Frontal_Cortex_BA9 16.719 -0.433 | 11215 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0027others(10): Show | HG00099.hp2 HG00323.hp1 HG00423.hp2 HG00438.hp2 HG00558.hp1 others(164): Show |
0.437 | 182 | 234 | 10 | chr12_48924763_G_A_b38 | - | MODIFIER | chr12 | G | A | TogoVar |
| 48924763:splice 48924763:variant goto | FKBP11intron_variantc.196-115C>T | FKBP11 Brain_Frontal_Cortex_BA9 13.331 -0.368 | 11215 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0027others(10): Show | HG00099.hp2 HG00323.hp1 HG00423.hp2 HG00438.hp2 HG00558.hp1 others(164): Show |
0.437 | 182 | 234 | 10 | chr12_48924763_G_A_b38 | - | MODIFIER | chr12 | G | A | TogoVar |
| 48924763:splice 48924763:variant goto | FKBP11intron_variantc.196-115C>T | WNT10B Brain_Frontal_Cortex_BA9 14.006 -0.287 | 11215 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0027others(10): Show | HG00099.hp2 HG00323.hp1 HG00423.hp2 HG00438.hp2 HG00558.hp1 others(164): Show |
0.437 | 182 | 234 | 10 | chr12_48924763_G_A_b38 | - | MODIFIER | chr12 | G | A | TogoVar |
| 48924763:splice 48924763:variant goto | FKBP11intron_variantc.196-115C>T | FKBP11 Brain_Hippocampus 7.107 -0.252 | 11215 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0027others(10): Show | HG00099.hp2 HG00323.hp1 HG00423.hp2 HG00438.hp2 HG00558.hp1 others(164): Show |
0.435 | 172 | 221 | 10 | chr12_48924763_G_A_b38 | - | MODIFIER | chr12 | G | A | TogoVar |
| 48924763:splice 48924763:variant goto | FKBP11intron_variantc.196-115C>T | FKBP11 Brain_Hypothalamus 4.282 -0.102 | 11215 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0027others(10): Show | HG00099.hp2 HG00323.hp1 HG00423.hp2 HG00438.hp2 HG00558.hp1 others(164): Show |
0.447 | 177 | 229 | 10 | chr12_48924763_G_A_b38 | - | MODIFIER | chr12 | G | A | TogoVar |
| 48924763:splice 48924763:variant goto | FKBP11intron_variantc.196-115C>T | CCDC65 Brain_Nucleus_accumbens_basal_ganglia 5.084 -0.155 | 11215 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0027others(10): Show | HG00099.hp2 HG00323.hp1 HG00423.hp2 HG00438.hp2 HG00558.hp1 others(164): Show |
0.445 | 196 | 253 | 10 | chr12_48924763_G_A_b38 | - | MODIFIER | chr12 | G | A | TogoVar |
| 48924763:splice 48924763:variant goto | FKBP11intron_variantc.196-115C>T | FKBP11 Brain_Nucleus_accumbens_basal_ganglia 15.400 -0.351 | 11215 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0027others(10): Show | HG00099.hp2 HG00323.hp1 HG00423.hp2 HG00438.hp2 HG00558.hp1 others(164): Show |
0.445 | 196 | 253 | 10 | chr12_48924763_G_A_b38 | - | MODIFIER | chr12 | G | A | TogoVar |
| 48924763:splice 48924763:variant goto | FKBP11intron_variantc.196-115C>T | CCDC65 Brain_Putamen_basal_ganglia 4.831 -0.175 | 11215 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0027others(10): Show | HG00099.hp2 HG00323.hp1 HG00423.hp2 HG00438.hp2 HG00558.hp1 others(164): Show |
0.439 | 174 | 222 | 10 | chr12_48924763_G_A_b38 | - | MODIFIER | chr12 | G | A | TogoVar |
| 48924763:splice 48924763:variant goto | FKBP11intron_variantc.196-115C>T | FKBP11 Brain_Putamen_basal_ganglia 10.739 -0.295 | 11215 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0027others(10): Show | HG00099.hp2 HG00323.hp1 HG00423.hp2 HG00438.hp2 HG00558.hp1 others(164): Show |
0.439 | 174 | 222 | 10 | chr12_48924763_G_A_b38 | - | MODIFIER | chr12 | G | A | TogoVar |
| 48924763:splice 48924763:variant goto | FKBP11intron_variantc.196-115C>T | CCDC65 Brain_Spinal_cord_cervical_c-1 4.084 -0.276 | 11215 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0027others(10): Show | HG00099.hp2 HG00323.hp1 HG00423.hp2 HG00438.hp2 HG00558.hp1 others(164): Show |
0.436 | 140 | 177 | 10 | chr12_48924763_G_A_b38 | - | MODIFIER | chr12 | G | A | TogoVar |
| 48924763:splice 48924763:variant goto | FKBP11intron_variantc.196-115C>T | CCDC65 Brain_Substantia_nigra 5.892 -0.299 | 11215 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0027others(10): Show | HG00099.hp2 HG00323.hp1 HG00423.hp2 HG00438.hp2 HG00558.hp1 others(164): Show |
0.415 | 123 | 152 | 10 | chr12_48924763_G_A_b38 | - | MODIFIER | chr12 | G | A | TogoVar |
| 48924763:splice 48924763:variant goto | FKBP11intron_variantc.196-115C>T | FKBP11 Brain_Substantia_nigra 6.371 -0.350 | 11215 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0027others(10): Show | HG00099.hp2 HG00323.hp1 HG00423.hp2 HG00438.hp2 HG00558.hp1 others(164): Show |
0.415 | 123 | 152 | 10 | chr12_48924763_G_A_b38 | - | MODIFIER | chr12 | G | A | TogoVar |
| 48924763:splice 48924763:variant goto | FKBP11intron_variantc.196-115C>T | CCDC65 Breast_Mammary_Tissue 18.878 -0.425 | 11215 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0027others(10): Show | HG00099.hp2 HG00323.hp1 HG00423.hp2 HG00438.hp2 HG00558.hp1 others(164): Show |
0.444 | 356 | 454 | 10 | chr12_48924763_G_A_b38 | - | MODIFIER | chr12 | G | A | TogoVar |
| 48924763:splice 48924763:variant goto | FKBP11intron_variantc.196-115C>T | FKBP11 Breast_Mammary_Tissue 11.534 -0.193 | 11215 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0027others(10): Show | HG00099.hp2 HG00323.hp1 HG00423.hp2 HG00438.hp2 HG00558.hp1 others(164): Show |
0.444 | 356 | 454 | 10 | chr12_48924763_G_A_b38 | - | MODIFIER | chr12 | G | A | TogoVar |
| 48924763:splice 48924763:variant goto | FKBP11intron_variantc.196-115C>T | CCDC65 Cells_Cultured_fibroblasts 28.392 -0.439 | 11215 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0027others(10): Show | HG00099.hp2 HG00323.hp1 HG00423.hp2 HG00438.hp2 HG00558.hp1 others(164): Show |
0.453 | 460 | 588 | 10 | chr12_48924763_G_A_b38 | - | MODIFIER | chr12 | G | A | TogoVar |
| 48924763:splice 48924763:variant goto | FKBP11intron_variantc.196-115C>T | FKBP11 Cells_Cultured_fibroblasts 21.650 -0.180 | 11215 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0027others(10): Show | HG00099.hp2 HG00323.hp1 HG00423.hp2 HG00438.hp2 HG00558.hp1 others(164): Show |
0.453 | 460 | 588 | 10 | chr12_48924763_G_A_b38 | - | MODIFIER | chr12 | G | A | TogoVar |
| 48924763:splice 48924763:variant goto | FKBP11intron_variantc.196-115C>T | ARF3 Cells_Cultured_fibroblasts 37.180 0.225 | 11215 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0027others(10): Show | HG00099.hp2 HG00323.hp1 HG00423.hp2 HG00438.hp2 HG00558.hp1 others(164): Show |
0.453 | 460 | 588 | 10 | chr12_48924763_G_A_b38 | - | MODIFIER | chr12 | G | A | TogoVar |
| 48924763:splice 48924763:variant goto | FKBP11intron_variantc.196-115C>T | CCDC65 Cells_EBV-transformed_lymphocytes 15.469 -0.569 | 11215 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0027others(10): Show | HG00099.hp2 HG00323.hp1 HG00423.hp2 HG00438.hp2 HG00558.hp1 others(164): Show |
0.449 | 228 | 293 | 10 | chr12_48924763_G_A_b38 | - | MODIFIER | chr12 | G | A | TogoVar |
| 48924763:splice 48924763:variant goto | FKBP11intron_variantc.196-115C>T | ARF3 Cells_EBV-transformed_lymphocytes 10.040 0.178 | 11215 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0027others(10): Show | HG00099.hp2 HG00323.hp1 HG00423.hp2 HG00438.hp2 HG00558.hp1 others(164): Show |
0.449 | 228 | 293 | 10 | chr12_48924763_G_A_b38 | - | MODIFIER | chr12 | G | A | TogoVar |
| 48924763:splice 48924763:variant goto | FKBP11intron_variantc.196-115C>T | CCDC65 Colon_Sigmoid 11.922 -0.378 | 11215 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0027others(10): Show | HG00099.hp2 HG00323.hp1 HG00423.hp2 HG00438.hp2 HG00558.hp1 others(164): Show |
0.427 | 283 | 357 | 10 | chr12_48924763_G_A_b38 | - | MODIFIER | chr12 | G | A | TogoVar |
| 48924763:splice 48924763:variant goto | FKBP11intron_variantc.196-115C>T | FKBP11 Colon_Sigmoid 6.237 -0.146 | 11215 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0027others(10): Show | HG00099.hp2 HG00323.hp1 HG00423.hp2 HG00438.hp2 HG00558.hp1 others(164): Show |
0.427 | 283 | 357 | 10 | chr12_48924763_G_A_b38 | - | MODIFIER | chr12 | G | A | TogoVar |
| 48924763:splice 48924763:variant goto | FKBP11intron_variantc.196-115C>T | CCDC65 Colon_Transverse 15.108 -0.345 | 11215 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0027others(10): Show | HG00099.hp2 HG00323.hp1 HG00423.hp2 HG00438.hp2 HG00558.hp1 others(164): Show |
0.440 | 330 | 421 | 10 | chr12_48924763_G_A_b38 | - | MODIFIER | chr12 | G | A | TogoVar |
| 48924763:splice 48924763:variant goto | FKBP11intron_variantc.196-115C>T | CCDC65 Esophagus_Gastroesophageal_Junction 21.571 -0.474 | 11215 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0027others(10): Show | HG00099.hp2 HG00323.hp1 HG00423.hp2 HG00438.hp2 HG00558.hp1 others(164): Show |
0.423 | 271 | 341 | 10 | chr12_48924763_G_A_b38 | - | MODIFIER | chr12 | G | A | TogoVar |