| geneid | 10881 |
|---|---|
| ensemblid | ENSG00000187003.7 |
| hgncid | 161 |
| symbol | ACTL7A |
| name | actin like 7A |
| refseq_nuc | NM_006687.4 |
| refseq_prot | NP_006678.1 |
| ensembl_nuc | ENST00000333999.5 |
| ensembl_prot | ENSP00000334300.3 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 108862266 |
| end | 108863756 |
| strand | + |
| ver | v1.2 |
| region | chr9:108862266-108863756 |
| region5000 | chr9:108857266-108868756 |
| regionname0 | ACTL7A_chr9_108862266_108863756 |
| regionname5000 | ACTL7A_chr9_108857266_108868756 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| ACTL7A | 1/1 | a0001 | 435 | 436 | 80 | 79 | 216 | 18 | 41 | subcellular location copy fasta | chr9 | 108857266 | 108868756 |
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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 108867626:splice 108867626:variant goto | c.*3996C>T | 913073 | Uncertain_significance | ELP1:8518 | SO:0001624 3_prime_UTR_variant |
MONDO:MONDO:0009131 MedGen:C0013364 OMIM:223900 Orphanet:1764|MedGen:C3661900 |
+ | 1 | 1 | 1 | 1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | NA18978.hp2 NA19066.hp2 |
MODIFIER | chr9 | C | T | TogoVar |
| 108867834:splice 108867834:variant goto | c.*4204A>G | 914223 | Uncertain_significance | ELP1:8518 | SO:0001624 3_prime_UTR_variant |
MONDO:MONDO:0009131 MedGen:C0013364 OMIM:223900 Orphanet:1764 |
+ | 1 | 1 | 1 | 1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | NA18994.hp1 | MODIFIER | chr9 | A | G | TogoVar |
| 108867901:splice 108867901:variant goto | c.*4271G>A | 364542 | Uncertain_significance | ELP1:8518 | SO:0001624 3_prime_UTR_variant |
MONDO:MONDO:0009131 MedGen:C0013364 OMIM:223900 Orphanet:1764 |
+ | 1 | 1 | 1 | 1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | HG01261.hp1 HG02809.hp2 HG02886.hp2 HG02970.hp2 |
MODIFIER | chr9 | G | A | TogoVar |
| 108867868:splice 108867868:variant goto | c.*4238A>G | 364541 | Likely_benign | ELP1:8518 | SO:0001624 3_prime_UTR_variant |
MONDO:MONDO:0009131 MedGen:C0013364 OMIM:223900 Orphanet:1764 |
+ | 1 | 1 | 2 | 2 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0000a0001c0001t0002g0000 | NA18612.hp2 NA18944.hp1 NA18966.hp1 NA18981.hp2 NA19007.hp2 others(1): Show |
MODIFIER | chr9 | A | G | TogoVar |
| 108867855:splice 108867855:variant goto | c.*4225G>A | 364538 | Benign | ELP1:8518 | SO:0001624 3_prime_UTR_variant |
MedGen:C3661900|MONDO:MONDO:0009131 MedGen:C0013364 OMIM:223900 Orphanet:1764 |
+ | 2 | 3 | 5 | 5 | a0001a0002 | a0001c0001a0002c0002a0002c0004 | a0001c0001t0001a0001c0001t0002a0001c0001t0003a0002c0002t0001a0002c0004t0001 | a0001c0001t0001g0000a0001c0001t0002g0000a0001c0001t0003g0000a0002c0002t0001g0000a0002c0004t0001g0000 | HG00280.hp1 HG00558.hp1 HG00639.hp2 HG01069.hp1 HG01074.hp2 others(58): Show |
MODIFIER | chr9 | G | A | TogoVar |
| 108867856:splice 108867856:variant goto | c.*4226G>C | 364539 | Benign | ELP1:8518 | SO:0001624 3_prime_UTR_variant |
MONDO:MONDO:0009131 MedGen:C0013364 OMIM:223900 Orphanet:1764|MedGen:C3661900 |
+ | 2 | 3 | 5 | 5 | a0001a0002 | a0001c0001a0002c0002a0002c0004 | a0001c0001t0001a0001c0001t0002a0001c0001t0003a0002c0002t0001a0002c0004t0001 | a0001c0001t0001g0000a0001c0001t0002g0000a0001c0001t0003g0000a0002c0002t0001g0000a0002c0004t0001g0000 | HG00280.hp1 HG00558.hp1 HG00639.hp2 HG01069.hp1 HG01074.hp2 others(58): Show |
MODIFIER | chr9 | G | C | TogoVar |
| 108867764:splice 108867764:variant goto | c.*4134G>T | 364536 | Benign | ELP1:8518 | SO:0001624 3_prime_UTR_variant |
MONDO:MONDO:0009131 MedGen:C0013364 OMIM:223900 Orphanet:1764|MedGen:C3661900 |
+ | 6 | 9 | 10 | 10 | a0001a0002a0003a0004a0005others(1): Show | a0001c0001a0001c0010a0001c0013a0002c0002a0002c0009others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0010t0001a0001c0013t0001a0002c0002t0001others(5): Show | a0001c0001t0001g0000a0001c0001t0002g0000a0001c0010t0001g0000a0001c0013t0001g0000a0002c0002t0001g0000others(5): Show | HG00280.hp2 HG00408.hp2 HG00438.hp1 HG00544.hp1 HG00544.hp2 others(213): Show |
MODIFIER | chr9 | G | T | TogoVar |
| 108868044:splice 108868044:variant goto | c.*4414C>T | 364545 | Benign | ELP1:8518 | SO:0001624 3_prime_UTR_variant |
MONDO:MONDO:0009131 MedGen:C0013364 OMIM:223900 Orphanet:1764|MedGen:C3661900 |
+ | 2 | 3 | 3 | 3 | a0001a0003 | a0001c0001a0001c0012a0003c0003 | a0001c0001t0001a0001c0012t0001a0003c0003t0001 | a0001c0001t0001g0000a0001c0012t0001g0000a0003c0003t0001g0000 | HG00099.hp2 HG00140.hp2 HG01106.hp1 HG01358.hp2 HG02109.hp2 others(21): Show |
MODIFIER | chr9 | C | T | TogoVar |
| 108868723:splice 108868723:variant goto | c.*5093T>C | 364549 | Benign | ELP1:8518 | SO:0001624 3_prime_UTR_variant |
MONDO:MONDO:0009131 MedGen:C0013364 OMIM:223900 Orphanet:1764|MedGen:C3661900 |
+ | 1 | 2 | 2 | 2 | a0001 | a0001c0001a0001c0013 | a0001c0001t0001a0001c0013t0001 | a0001c0001t0001g0000a0001c0013t0001g0000 | HG00609.hp1 HG00609.hp2 HG01261.hp1 HG02132.hp1 HG02809.hp2 others(24): Show |
MODIFIER | chr9 | T | C | TogoVar |
| 108868254:splice 108868254:variant goto | c.*4624A>C | 364547 | Benign | ELP1:8518 | SO:0001624 3_prime_UTR_variant |
MONDO:MONDO:0009131 MedGen:C0013364 OMIM:223900 Orphanet:1764 |
+ | 2 | 2 | 2 | 2 | a0001a0003 | a0001c0001a0003c0003 | a0001c0001t0001a0003c0003t0001 | a0001c0001t0001g0000a0003c0003t0001g0000 | HG00733.hp2 HG01109.hp2 HG02055.hp2 HG02145.hp2 HG02257.hp2 others(7): Show |
MODIFIER | chr9 | A | C | TogoVar |
| 108868053:splice 108868053:variant goto | c.*4423C>A | 364546 | Uncertain_significance | ELP1:8518 | SO:0001624 3_prime_UTR_variant |
MONDO:MONDO:0009131 MedGen:C0013364 OMIM:223900 Orphanet:1764 |
+ | 1 | 1 | 1 | 1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0000 | HG03669.hp2 | MODIFIER | chr9 | C | A | TogoVar |
| 108868613:splice 108868613:variant goto | c.*4983G>A | 364548 | Uncertain_significance | ELP1:8518 | SO:0001624 3_prime_UTR_variant |
MONDO:MONDO:0009131 MedGen:C0013364 OMIM:223900 Orphanet:1764 |
+ | 1 | 1 | 1 | 1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0000 | NA18971.hp2 NA18995.hp2 |
MODIFIER | chr9 | G | A | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
chr9:108858025
|
c.-4298C>T | Bone mineral density mean | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | HG00099.hp2 |
A longitudinal genome-wide association study of bo others(58): Show |
5,862 South Asian ancestry individuals/ | ACTL7B - ACTL7A | rs148677168-? | + | MODIFIER | chr9 | C | T |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 108860695:splice 108860695:variant goto | ACTL7Aupstream_gene_variantc.-1628G>Aothers(2): Show | ELP1 Adipose_Subcutaneous 8.237 0.218 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | HG00099.hp1 HG00099.hp2 HG00140.hp2 HG01106.hp1 HG01358.hp2 others(4): Show |
0.096 | 128 | 136 | 10 | chr9_108860695_G_A_b38 | + | MODIFIER | chr9 | G | A | TogoVar |
| 108861837:splice 108861837:variant goto | ACTL7Aupstream_gene_variantc.-486C>Gothers(1): Show | ABITRAM Adipose_Subcutaneous 4.015 -0.459 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | HG01433.hp2 HG01496.hp1 HG02300.hp2 |
0.014 | 20 | 20 | 10 | chr9_108861837_C_G_b38 | + | MODIFIER | chr9 | C | G | TogoVar |
| 108858025:splice 108858025:variant goto | ACTL7Aupstream_gene_variantc.-4298C>Tothers(2): Show | CTNNAL1 Adipose_Subcutaneous 4.590 -0.476 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | HG00099.hp2 | 0.027 | 38 | 38 | 10 | chr9_108858025_C_T_b38 | + | MODIFIER | chr9 | C | T | TogoVar |
| 108860695:splice 108860695:variant goto | ACTL7Aupstream_gene_variantc.-1628G>Aothers(2): Show | CTNNAL1 Adipose_Subcutaneous 17.195 -0.518 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | HG00099.hp1 HG00099.hp2 HG00140.hp2 HG01106.hp1 HG01358.hp2 others(4): Show |
0.096 | 128 | 136 | 10 | chr9_108860695_G_A_b38 | + | MODIFIER | chr9 | G | A | TogoVar |
| 108861837:splice 108861837:variant goto | ACTL7Aupstream_gene_variantc.-486C>Gothers(1): Show | CTNNAL1 Adipose_Subcutaneous 8.352 0.898 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | HG01433.hp2 HG01496.hp1 HG02300.hp2 |
0.014 | 20 | 20 | 10 | chr9_108861837_C_G_b38 | + | MODIFIER | chr9 | C | G | TogoVar |
| 108860695:splice 108860695:variant goto | ACTL7Aupstream_gene_variantc.-1628G>Aothers(2): Show | ELP1 Adipose_Visceral_Omentum 5.912 0.212 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | HG00099.hp1 HG00099.hp2 HG00140.hp2 HG01106.hp1 HG01358.hp2 others(4): Show |
0.098 | 110 | 115 | 10 | chr9_108860695_G_A_b38 | + | MODIFIER | chr9 | G | A | TogoVar |
| 108860695:splice 108860695:variant goto | ACTL7Aupstream_gene_variantc.-1628G>Aothers(2): Show | CTNNAL1 Adipose_Visceral_Omentum 10.241 -0.343 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | HG00099.hp1 HG00099.hp2 HG00140.hp2 HG01106.hp1 HG01358.hp2 others(4): Show |
0.098 | 110 | 115 | 10 | chr9_108860695_G_A_b38 | + | MODIFIER | chr9 | G | A | TogoVar |
| 108860695:splice 108860695:variant goto | ACTL7Aupstream_gene_variantc.-1628G>Aothers(2): Show | ELP1 Artery_Aorta 7.823 0.257 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | HG00099.hp1 HG00099.hp2 HG00140.hp2 HG01106.hp1 HG01358.hp2 others(4): Show |
0.102 | 89 | 96 | 10 | chr9_108860695_G_A_b38 | + | MODIFIER | chr9 | G | A | TogoVar |
| 108861837:splice 108861837:variant goto | ACTL7Aupstream_gene_variantc.-486C>Gothers(1): Show | CTNNAL1 Artery_Aorta 4.052 0.648 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | HG01433.hp2 HG01496.hp1 HG02300.hp2 |
0.014 | 13 | 13 | 10 | chr9_108861837_C_G_b38 | + | MODIFIER | chr9 | C | G | TogoVar |
| 108860695:splice 108860695:variant goto | ACTL7Aupstream_gene_variantc.-1628G>Aothers(2): Show | ELP1 Artery_Coronary 4.975 0.234 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | HG00099.hp1 HG00099.hp2 HG00140.hp2 HG01106.hp1 HG01358.hp2 others(4): Show |
0.119 | 59 | 64 | 10 | chr9_108860695_G_A_b38 | + | MODIFIER | chr9 | G | A | TogoVar |
| 108860695:splice 108860695:variant goto | ACTL7Aupstream_gene_variantc.-1628G>Aothers(2): Show | ELP1 Artery_Tibial 10.003 0.198 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | HG00099.hp1 HG00099.hp2 HG00140.hp2 HG01106.hp1 HG01358.hp2 others(4): Show |
0.096 | 125 | 132 | 10 | chr9_108860695_G_A_b38 | + | MODIFIER | chr9 | G | A | TogoVar |
| 108858025:splice 108858025:variant goto | ACTL7Aupstream_gene_variantc.-4298C>Tothers(2): Show | CTNNAL1 Artery_Tibial 5.712 -0.483 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | HG00099.hp2 | 0.024 | 32 | 33 | 10 | chr9_108858025_C_T_b38 | + | MODIFIER | chr9 | C | T | TogoVar |
| 108860695:splice 108860695:variant goto | ACTL7Aupstream_gene_variantc.-1628G>Aothers(2): Show | CTNNAL1 Artery_Tibial 16.274 -0.449 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | HG00099.hp1 HG00099.hp2 HG00140.hp2 HG01106.hp1 HG01358.hp2 others(4): Show |
0.096 | 125 | 132 | 10 | chr9_108860695_G_A_b38 | + | MODIFIER | chr9 | G | A | TogoVar |
| 108861837:splice 108861837:variant goto | ACTL7Aupstream_gene_variantc.-486C>Gothers(1): Show | CTNNAL1 Artery_Tibial 6.134 0.656 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | HG01433.hp2 HG01496.hp1 HG02300.hp2 |
0.015 | 21 | 21 | 10 | chr9_108861837_C_G_b38 | + | MODIFIER | chr9 | C | G | TogoVar |
| 108860695:splice 108860695:variant goto | ACTL7Aupstream_gene_variantc.-1628G>Aothers(2): Show | CTNNAL1 Brain_Caudate_basal_ganglia 4.071 -0.282 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | HG00099.hp1 HG00099.hp2 HG00140.hp2 HG01106.hp1 HG01358.hp2 others(4): Show |
0.101 | 59 | 60 | 10 | chr9_108860695_G_A_b38 | + | MODIFIER | chr9 | G | A | TogoVar |
| 108860695:splice 108860695:variant goto | ACTL7Aupstream_gene_variantc.-1628G>Aothers(2): Show | ELP1 Brain_Cerebellar_Hemisphere 4.479 0.199 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | HG00099.hp1 HG00099.hp2 HG00140.hp2 HG01106.hp1 HG01358.hp2 others(4): Show |
0.101 | 55 | 56 | 10 | chr9_108860695_G_A_b38 | + | MODIFIER | chr9 | G | A | TogoVar |
| 108860695:splice 108860695:variant goto | ACTL7Aupstream_gene_variantc.-1628G>Aothers(2): Show | CTNNAL1 Brain_Cerebellar_Hemisphere 4.553 -0.320 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | HG00099.hp1 HG00099.hp2 HG00140.hp2 HG01106.hp1 HG01358.hp2 others(4): Show |
0.101 | 55 | 56 | 10 | chr9_108860695_G_A_b38 | + | MODIFIER | chr9 | G | A | TogoVar |
| 108861837:splice 108861837:variant goto | ACTL7Aupstream_gene_variantc.-486C>Gothers(1): Show | CTNNAL1 Brain_Cerebellar_Hemisphere 3.986 0.690 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | HG01433.hp2 HG01496.hp1 HG02300.hp2 |
0.016 | 9 | 9 | 10 | chr9_108861837_C_G_b38 | + | MODIFIER | chr9 | C | G | TogoVar |
| 108860695:splice 108860695:variant goto | ACTL7Aupstream_gene_variantc.-1628G>Aothers(2): Show | ELP1 Brain_Cerebellum 4.602 0.248 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | HG00099.hp1 HG00099.hp2 HG00140.hp2 HG01106.hp1 HG01358.hp2 others(4): Show |
0.098 | 51 | 52 | 10 | chr9_108860695_G_A_b38 | + | MODIFIER | chr9 | G | A | TogoVar |
| 108861837:splice 108861837:variant goto | ACTL7Aupstream_gene_variantc.-486C>Gothers(1): Show | CTNNAL1 Brain_Hypothalamus 6.550 0.861 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | HG01433.hp2 HG01496.hp1 HG02300.hp2 |
0.020 | 10 | 10 | 10 | chr9_108861837_C_G_b38 | + | MODIFIER | chr9 | C | G | TogoVar |
| 108861837:splice 108861837:variant goto | ACTL7Aupstream_gene_variantc.-486C>Gothers(1): Show | CTNNAL1 Brain_Putamen_basal_ganglia 4.711 0.826 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | HG01433.hp2 HG01496.hp1 HG02300.hp2 |
0.014 | 7 | 7 | 10 | chr9_108861837_C_G_b38 | + | MODIFIER | chr9 | C | G | TogoVar |
| 108861837:splice 108861837:variant goto | ACTL7Aupstream_gene_variantc.-486C>Gothers(1): Show | CTNNAL1 Brain_Spinal_cord_cervical_c-1 6.430 1.202 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | HG01433.hp2 HG01496.hp1 HG02300.hp2 |
0.017 | 7 | 7 | 10 | chr9_108861837_C_G_b38 | + | MODIFIER | chr9 | C | G | TogoVar |
| 108860695:splice 108860695:variant goto | ACTL7Aupstream_gene_variantc.-1628G>Aothers(2): Show | CTNNAL1 Brain_Substantia_nigra 4.907 -0.479 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | HG00099.hp1 HG00099.hp2 HG00140.hp2 HG01106.hp1 HG01358.hp2 others(4): Show |
0.109 | 38 | 40 | 10 | chr9_108860695_G_A_b38 | + | MODIFIER | chr9 | G | A | TogoVar |
| 108861837:splice 108861837:variant goto | ACTL7Aupstream_gene_variantc.-486C>Gothers(1): Show | CTNNAL1 Brain_Substantia_nigra 4.643 1.213 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | HG01433.hp2 HG01496.hp1 HG02300.hp2 |
0.014 | 5 | 5 | 10 | chr9_108861837_C_G_b38 | + | MODIFIER | chr9 | C | G | TogoVar |
| 108860695:splice 108860695:variant goto | ACTL7Aupstream_gene_variantc.-1628G>Aothers(2): Show | ELP1 Breast_Mammary_Tissue 7.313 0.224 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | HG00099.hp1 HG00099.hp2 HG00140.hp2 HG01106.hp1 HG01358.hp2 others(4): Show |
0.106 | 100 | 108 | 10 | chr9_108860695_G_A_b38 | + | MODIFIER | chr9 | G | A | TogoVar |
| 108861837:splice 108861837:variant goto | ACTL7Aupstream_gene_variantc.-486C>Gothers(1): Show | ELP1 Breast_Mammary_Tissue 5.329 -0.510 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | HG01433.hp2 HG01496.hp1 HG02300.hp2 |
0.014 | 14 | 14 | 10 | chr9_108861837_C_G_b38 | + | MODIFIER | chr9 | C | G | TogoVar |
| 108860695:splice 108860695:variant goto | ACTL7Aupstream_gene_variantc.-1628G>Aothers(2): Show | CTNNAL1 Breast_Mammary_Tissue 8.334 -0.302 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | HG00099.hp1 HG00099.hp2 HG00140.hp2 HG01106.hp1 HG01358.hp2 others(4): Show |
0.106 | 100 | 108 | 10 | chr9_108860695_G_A_b38 | + | MODIFIER | chr9 | G | A | TogoVar |
| 108860695:splice 108860695:variant goto | ACTL7Aupstream_gene_variantc.-1628G>Aothers(2): Show | ELP1 Cells_Cultured_fibroblasts 5.650 0.154 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | HG00099.hp1 HG00099.hp2 HG00140.hp2 HG01106.hp1 HG01358.hp2 others(4): Show |
0.096 | 118 | 125 | 10 | chr9_108860695_G_A_b38 | + | MODIFIER | chr9 | G | A | TogoVar |
| 108861837:splice 108861837:variant goto | ACTL7Aupstream_gene_variantc.-486C>Gothers(1): Show | ABITRAM Cells_Cultured_fibroblasts 3.834 -0.471 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | HG01433.hp2 HG01496.hp1 HG02300.hp2 |
0.015 | 20 | 20 | 10 | chr9_108861837_C_G_b38 | + | MODIFIER | chr9 | C | G | TogoVar |
| 108860695:splice 108860695:variant goto | ACTL7Aupstream_gene_variantc.-1628G>Aothers(2): Show | CTNNAL1 Cells_Cultured_fibroblasts 6.201 -0.128 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | HG00099.hp1 HG00099.hp2 HG00140.hp2 HG01106.hp1 HG01358.hp2 others(4): Show |
0.096 | 118 | 125 | 10 | chr9_108860695_G_A_b38 | + | MODIFIER | chr9 | G | A | TogoVar |
| 108861837:splice 108861837:variant goto | ACTL7Aupstream_gene_variantc.-486C>Gothers(1): Show | CTNNAL1 Cells_Cultured_fibroblasts 5.042 0.274 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | HG01433.hp2 HG01496.hp1 HG02300.hp2 |
0.015 | 20 | 20 | 10 | chr9_108861837_C_G_b38 | + | MODIFIER | chr9 | C | G | TogoVar |
| 108860695:splice 108860695:variant goto | ACTL7Aupstream_gene_variantc.-1628G>Aothers(2): Show | ELP1 Colon_Sigmoid 6.831 0.285 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | HG00099.hp1 HG00099.hp2 HG00140.hp2 HG01106.hp1 HG01358.hp2 others(4): Show |
0.096 | 76 | 80 | 10 | chr9_108860695_G_A_b38 | + | MODIFIER | chr9 | G | A | TogoVar |
| 108860695:splice 108860695:variant goto | ACTL7Aupstream_gene_variantc.-1628G>Aothers(2): Show | CTNNAL1 Colon_Sigmoid 4.522 -0.231 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | HG00099.hp1 HG00099.hp2 HG00140.hp2 HG01106.hp1 HG01358.hp2 others(4): Show |
0.096 | 76 | 80 | 10 | chr9_108860695_G_A_b38 | + | MODIFIER | chr9 | G | A | TogoVar |
| 108860695:splice 108860695:variant goto | ACTL7Aupstream_gene_variantc.-1628G>Aothers(2): Show | ELP1 Colon_Transverse 4.191 0.171 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | HG00099.hp1 HG00099.hp2 HG00140.hp2 HG01106.hp1 HG01358.hp2 others(4): Show |
0.110 | 97 | 105 | 10 | chr9_108860695_G_A_b38 | + | MODIFIER | chr9 | G | A | TogoVar |
| 108860695:splice 108860695:variant goto | ACTL7Aupstream_gene_variantc.-1628G>Aothers(2): Show | CTNNAL1 Colon_Transverse 4.589 -0.133 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | HG00099.hp1 HG00099.hp2 HG00140.hp2 HG01106.hp1 HG01358.hp2 others(4): Show |
0.110 | 97 | 105 | 10 | chr9_108860695_G_A_b38 | + | MODIFIER | chr9 | G | A | TogoVar |
| 108860695:splice 108860695:variant goto | ACTL7Aupstream_gene_variantc.-1628G>Aothers(2): Show | ELP1 Esophagus_Gastroesophageal_Junction 7.265 0.292 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | HG00099.hp1 HG00099.hp2 HG00140.hp2 HG01106.hp1 HG01358.hp2 others(4): Show |
0.100 | 76 | 81 | 10 | chr9_108860695_G_A_b38 | + | MODIFIER | chr9 | G | A | TogoVar |
| 108860695:splice 108860695:variant goto | ACTL7Aupstream_gene_variantc.-1628G>Aothers(2): Show | ELP1 Esophagus_Mucosa 4.791 0.165 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | HG00099.hp1 HG00099.hp2 HG00140.hp2 HG01106.hp1 HG01358.hp2 others(4): Show |
0.103 | 118 | 126 | 10 | chr9_108860695_G_A_b38 | + | MODIFIER | chr9 | G | A | TogoVar |
| 108860695:splice 108860695:variant goto | ACTL7Aupstream_gene_variantc.-1628G>Aothers(2): Show | ELP1 Esophagus_Muscularis 8.108 0.242 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | HG00099.hp1 HG00099.hp2 HG00140.hp2 HG01106.hp1 HG01358.hp2 others(4): Show |
0.108 | 114 | 121 | 10 | chr9_108860695_G_A_b38 | + | MODIFIER | chr9 | G | A | TogoVar |
| 108860695:splice 108860695:variant goto | ACTL7Aupstream_gene_variantc.-1628G>Aothers(2): Show | FRRS1L Esophagus_Muscularis 4.009 -0.208 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | HG00099.hp1 HG00099.hp2 HG00140.hp2 HG01106.hp1 HG01358.hp2 others(4): Show |
0.108 | 114 | 121 | 10 | chr9_108860695_G_A_b38 | + | MODIFIER | chr9 | G | A | TogoVar |
| 108860695:splice 108860695:variant goto | ACTL7Aupstream_gene_variantc.-1628G>Aothers(2): Show | ELP1 Heart_Atrial_Appendage 4.500 0.229 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | HG00099.hp1 HG00099.hp2 HG00140.hp2 HG01106.hp1 HG01358.hp2 others(4): Show |
0.103 | 90 | 95 | 10 | chr9_108860695_G_A_b38 | + | MODIFIER | chr9 | G | A | TogoVar |
| 108861837:splice 108861837:variant goto | ACTL7Aupstream_gene_variantc.-486C>Gothers(1): Show | ABITRAM Liver 5.909 -1.239 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | HG01433.hp2 HG01496.hp1 HG02300.hp2 |
0.010 | 5 | 5 | 10 | chr9_108861837_C_G_b38 | + | MODIFIER | chr9 | C | G | TogoVar |
| 108860695:splice 108860695:variant goto | ACTL7Aupstream_gene_variantc.-1628G>Aothers(2): Show | ELP1 Lung 10.088 0.265 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | HG00099.hp1 HG00099.hp2 HG00140.hp2 HG01106.hp1 HG01358.hp2 others(4): Show |
0.106 | 119 | 127 | 10 | chr9_108860695_G_A_b38 | + | MODIFIER | chr9 | G | A | TogoVar |
| 108860695:splice 108860695:variant goto | ACTL7Aupstream_gene_variantc.-1628G>Aothers(2): Show | CTNNAL1 Lung 7.327 -0.205 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | HG00099.hp1 HG00099.hp2 HG00140.hp2 HG01106.hp1 HG01358.hp2 others(4): Show |
0.106 | 119 | 127 | 10 | chr9_108860695_G_A_b38 | + | MODIFIER | chr9 | G | A | TogoVar |
| 108861837:splice 108861837:variant goto | ACTL7Aupstream_gene_variantc.-486C>Gothers(1): Show | CTNNAL1 Lung 6.797 0.588 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | HG01433.hp2 HG01496.hp1 HG02300.hp2 |
0.011 | 13 | 13 | 10 | chr9_108861837_C_G_b38 | + | MODIFIER | chr9 | C | G | TogoVar |
| 108861837:splice 108861837:variant goto | ACTL7Aupstream_gene_variantc.-486C>Gothers(1): Show | CTNNAL1 Minor_Salivary_Gland 7.066 1.182 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | HG01433.hp2 HG01496.hp1 HG02300.hp2 |
0.019 | 7 | 7 | 10 | chr9_108861837_C_G_b38 | + | MODIFIER | chr9 | C | G | TogoVar |
| 108860695:splice 108860695:variant goto | ACTL7Aupstream_gene_variantc.-1628G>Aothers(2): Show | CTNNAL1 Muscle_Skeletal 13.533 -0.420 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | HG00099.hp1 HG00099.hp2 HG00140.hp2 HG01106.hp1 HG01358.hp2 others(4): Show |
0.102 | 156 | 166 | 10 | chr9_108860695_G_A_b38 | + | MODIFIER | chr9 | G | A | TogoVar |
| 108861837:splice 108861837:variant goto | ACTL7Aupstream_gene_variantc.-486C>Gothers(1): Show | CTNNAL1 Muscle_Skeletal 15.820 1.166 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | HG01433.hp2 HG01496.hp1 HG02300.hp2 |
0.013 | 22 | 22 | 10 | chr9_108861837_C_G_b38 | + | MODIFIER | chr9 | C | G | TogoVar |
| 108860695:splice 108860695:variant goto | ACTL7Aupstream_gene_variantc.-1628G>Aothers(2): Show | EPB41L4B Muscle_Skeletal 5.709 0.202 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | HG00099.hp1 HG00099.hp2 HG00140.hp2 HG01106.hp1 HG01358.hp2 others(4): Show |
0.102 | 156 | 166 | 10 | chr9_108860695_G_A_b38 | + | MODIFIER | chr9 | G | A | TogoVar |
| 108858025:splice 108858025:variant goto | ACTL7Aupstream_gene_variantc.-4298C>Tothers(2): Show | ELP1 Nerve_Tibial 3.690 0.187 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | HG00099.hp2 | 0.025 | 34 | 34 | 10 | chr9_108858025_C_T_b38 | + | MODIFIER | chr9 | C | T | TogoVar |
| 108860695:splice 108860695:variant goto | ACTL7Aupstream_gene_variantc.-1628G>Aothers(2): Show | ELP1 Nerve_Tibial 11.747 0.191 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | HG00099.hp1 HG00099.hp2 HG00140.hp2 HG01106.hp1 HG01358.hp2 others(4): Show |
0.092 | 118 | 123 | 10 | chr9_108860695_G_A_b38 | + | MODIFIER | chr9 | G | A | TogoVar |
| 108858025:splice 108858025:variant goto | ACTL7Aupstream_gene_variantc.-4298C>Tothers(2): Show | CTNNAL1 Nerve_Tibial 4.977 -0.261 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | HG00099.hp2 | 0.025 | 34 | 34 | 10 | chr9_108858025_C_T_b38 | + | MODIFIER | chr9 | C | T | TogoVar |
| 108860695:splice 108860695:variant goto | ACTL7Aupstream_gene_variantc.-1628G>Aothers(2): Show | CTNNAL1 Nerve_Tibial 14.018 -0.246 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | HG00099.hp1 HG00099.hp2 HG00140.hp2 HG01106.hp1 HG01358.hp2 others(4): Show |
0.092 | 118 | 123 | 10 | chr9_108860695_G_A_b38 | + | MODIFIER | chr9 | G | A | TogoVar |
| 108860695:splice 108860695:variant goto | ACTL7Aupstream_gene_variantc.-1628G>Aothers(2): Show | ELP1 Pancreas 4.013 0.213 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | HG00099.hp1 HG00099.hp2 HG00140.hp2 HG01106.hp1 HG01358.hp2 others(4): Show |
0.112 | 76 | 81 | 10 | chr9_108860695_G_A_b38 | + | MODIFIER | chr9 | G | A | TogoVar |
| 108860695:splice 108860695:variant goto | ACTL7Aupstream_gene_variantc.-1628G>Aothers(2): Show | CTNNAL1 Pancreas 11.481 -0.513 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | HG00099.hp1 HG00099.hp2 HG00140.hp2 HG01106.hp1 HG01358.hp2 others(4): Show |
0.112 | 76 | 81 | 10 | chr9_108860695_G_A_b38 | + | MODIFIER | chr9 | G | A | TogoVar |
| 108860695:splice 108860695:variant goto | ACTL7Aupstream_gene_variantc.-1628G>Aothers(2): Show | ELP1 Prostate 5.624 0.308 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | HG00099.hp1 HG00099.hp2 HG00140.hp2 HG01106.hp1 HG01358.hp2 others(4): Show |
0.107 | 57 | 60 | 10 | chr9_108860695_G_A_b38 | + | MODIFIER | chr9 | G | A | TogoVar |
| 108860695:splice 108860695:variant goto | ACTL7Aupstream_gene_variantc.-1628G>Aothers(2): Show | ELP1 Skin_Not_Sun_Exposed_Suprapubic 4.794 0.169 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | HG00099.hp1 HG00099.hp2 HG00140.hp2 HG01106.hp1 HG01358.hp2 others(4): Show |
0.097 | 120 | 126 | 10 | chr9_108860695_G_A_b38 | + | MODIFIER | chr9 | G | A | TogoVar |
| 108858025:splice 108858025:variant goto | ACTL7Aupstream_gene_variantc.-4298C>Tothers(2): Show | CTNNAL1 Skin_Not_Sun_Exposed_Suprapubic 4.648 -0.343 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | HG00099.hp2 | 0.029 | 36 | 37 | 10 | chr9_108858025_C_T_b38 | + | MODIFIER | chr9 | C | T | TogoVar |
| 108860695:splice 108860695:variant goto | ACTL7Aupstream_gene_variantc.-1628G>Aothers(2): Show | CTNNAL1 Skin_Not_Sun_Exposed_Suprapubic 10.462 -0.306 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | HG00099.hp1 HG00099.hp2 HG00140.hp2 HG01106.hp1 HG01358.hp2 others(4): Show |
0.097 | 120 | 126 | 10 | chr9_108860695_G_A_b38 | + | MODIFIER | chr9 | G | A | TogoVar |
| 108858025:splice 108858025:variant goto | ACTL7Aupstream_gene_variantc.-4298C>Tothers(2): Show | CTNNAL1 Skin_Sun_Exposed_Lower_leg 3.809 -0.301 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | HG00099.hp2 | 0.027 | 40 | 41 | 10 | chr9_108858025_C_T_b38 | + | MODIFIER | chr9 | C | T | TogoVar |
| 108860695:splice 108860695:variant goto | ACTL7Aupstream_gene_variantc.-1628G>Aothers(2): Show | CTNNAL1 Skin_Sun_Exposed_Lower_leg 13.882 -0.337 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | HG00099.hp1 HG00099.hp2 HG00140.hp2 HG01106.hp1 HG01358.hp2 others(4): Show |
0.100 | 143 | 150 | 10 | chr9_108860695_G_A_b38 | + | MODIFIER | chr9 | G | A | TogoVar |
| 108860695:splice 108860695:variant goto | ACTL7Aupstream_gene_variantc.-1628G>Aothers(2): Show | ELP1 Spleen 5.058 0.255 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | HG00099.hp1 HG00099.hp2 HG00140.hp2 HG01106.hp1 HG01358.hp2 others(4): Show |
0.119 | 59 | 66 | 10 | chr9_108860695_G_A_b38 | + | MODIFIER | chr9 | G | A | TogoVar |
| 108860695:splice 108860695:variant goto | ACTL7Aupstream_gene_variantc.-1628G>Aothers(2): Show | CTNNAL1 Spleen 7.962 -0.389 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | HG00099.hp1 HG00099.hp2 HG00140.hp2 HG01106.hp1 HG01358.hp2 others(4): Show |
0.119 | 59 | 66 | 10 | chr9_108860695_G_A_b38 | + | MODIFIER | chr9 | G | A | TogoVar |
| 108860695:splice 108860695:variant goto | ACTL7Aupstream_gene_variantc.-1628G>Aothers(2): Show | CTNNAL1 Stomach 5.463 -0.186 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | HG00099.hp1 HG00099.hp2 HG00140.hp2 HG01106.hp1 HG01358.hp2 others(4): Show |
0.108 | 82 | 88 | 10 | chr9_108860695_G_A_b38 | + | MODIFIER | chr9 | G | A | TogoVar |
| 108860695:splice 108860695:variant goto | ACTL7Aupstream_gene_variantc.-1628G>Aothers(2): Show | ELP1 Thyroid 4.767 0.198 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | HG00099.hp1 HG00099.hp2 HG00140.hp2 HG01106.hp1 HG01358.hp2 others(4): Show |
0.105 | 135 | 143 | 10 | chr9_108860695_G_A_b38 | + | MODIFIER | chr9 | G | A | TogoVar |
| 108860695:splice 108860695:variant goto | ACTL7Aupstream_gene_variantc.-1628G>Aothers(2): Show | CTNNAL1 Thyroid 3.907 -0.120 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | HG00099.hp1 HG00099.hp2 HG00140.hp2 HG01106.hp1 HG01358.hp2 others(4): Show |
0.105 | 135 | 143 | 10 | chr9_108860695_G_A_b38 | + | MODIFIER | chr9 | G | A | TogoVar |
| 108860695:splice 108860695:variant goto | ACTL7Aupstream_gene_variantc.-1628G>Aothers(2): Show | ELP1 Whole_Blood 4.018 0.111 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | HG00099.hp1 HG00099.hp2 HG00140.hp2 HG01106.hp1 HG01358.hp2 others(4): Show |
0.101 | 151 | 161 | 10 | chr9_108860695_G_A_b38 | + | MODIFIER | chr9 | G | A | TogoVar |
| 108861837:splice 108861837:variant goto | ACTL7Aupstream_gene_variantc.-486C>Gothers(1): Show | CTNNAL1 Whole_Blood 6.233 0.404 | 1111 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | HG01433.hp2 HG01496.hp1 HG02300.hp2 |
0.014 | 23 | 23 | 10 | chr9_108861837_C_G_b38 | + | MODIFIER | chr9 | C | G | TogoVar |
| 108865909:splice 108865909:variant goto | ACTL7Adownstream_gene_variantc.*2279T>G< others(4): Show |
ABITRAM Artery_Aorta 5.093 -0.400 | 1122 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0000a0001c0001t0002g0000 | HG00408.hp2 HG00423.hp2 HG00621.hp1 HG01081.hp2 HG01099.hp2 others(43): Show |
0.042 | 38 | 40 | 10 | chr9_108865909_T_G_b38 | + | MODIFIER | chr9 | T | G | TogoVar |
| 108865909:splice 108865909:variant goto | ACTL7Adownstream_gene_variantc.*2279T>G< others(4): Show |
ABITRAM Artery_Tibial 3.852 -0.251 | 1122 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0000a0001c0001t0002g0000 | HG00408.hp2 HG00423.hp2 HG00621.hp1 HG01081.hp2 HG01099.hp2 others(43): Show |
0.054 | 70 | 74 | 10 | chr9_108865909_T_G_b38 | + | MODIFIER | chr9 | T | G | TogoVar |
| 108865909:splice 108865909:variant goto | ACTL7Adownstream_gene_variantc.*2279T>G< others(4): Show |
ELP1 Brain_Cerebellar_Hemisphere 5.355 -0.251 | 1122 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0000a0001c0001t0002g0000 | HG00408.hp2 HG00423.hp2 HG00621.hp1 HG01081.hp2 HG01099.hp2 others(43): Show |
0.062 | 32 | 34 | 10 | chr9_108865909_T_G_b38 | + | MODIFIER | chr9 | T | G | TogoVar |
| 108865909:splice 108865909:variant goto | ACTL7Adownstream_gene_variantc.*2279T>G< others(4): Show |
ELP1 Brain_Cerebellum 4.093 -0.281 | 1122 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0000a0001c0001t0002g0000 | HG00408.hp2 HG00423.hp2 HG00621.hp1 HG01081.hp2 HG01099.hp2 others(43): Show |
0.053 | 26 | 28 | 10 | chr9_108865909_T_G_b38 | + | MODIFIER | chr9 | T | G | TogoVar |
| 108865909:splice 108865909:variant goto | ACTL7Adownstream_gene_variantc.*2279T>G< others(4): Show |
ABITRAM Heart_Atrial_Appendage 4.659 -0.444 | 1122 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0000a0001c0001t0002g0000 | HG00408.hp2 HG00423.hp2 HG00621.hp1 HG01081.hp2 HG01099.hp2 others(43): Show |
0.050 | 44 | 46 | 10 | chr9_108865909_T_G_b38 | + | MODIFIER | chr9 | T | G | TogoVar |
| 108865909:splice 108865909:variant goto | ACTL7Adownstream_gene_variantc.*2279T>G< others(4): Show |
ABITRAM Lung 5.510 -0.236 | 1122 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0000a0001c0001t0002g0000 | HG00408.hp2 HG00423.hp2 HG00621.hp1 HG01081.hp2 HG01099.hp2 others(43): Show |
0.051 | 59 | 61 | 10 | chr9_108865909_T_G_b38 | + | MODIFIER | chr9 | T | G | TogoVar |
| 108865909:splice 108865909:variant goto | ACTL7Adownstream_gene_variantc.*2279T>G< others(4): Show |
ABITRAM Skin_Not_Sun_Exposed_Suprapubic 5.279 -0.237 | 1122 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0000a0001c0001t0002g0000 | HG00408.hp2 HG00423.hp2 HG00621.hp1 HG01081.hp2 HG01099.hp2 others(43): Show |
0.054 | 67 | 70 | 10 | chr9_108865909_T_G_b38 | + | MODIFIER | chr9 | T | G | TogoVar |
| 108865909:splice 108865909:variant goto | ACTL7Adownstream_gene_variantc.*2279T>G< others(4): Show |
ABITRAM Skin_Sun_Exposed_Lower_leg 7.883 -0.276 | 1122 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0000a0001c0001t0002g0000 | HG00408.hp2 HG00423.hp2 HG00621.hp1 HG01081.hp2 HG01099.hp2 others(43): Show |
0.048 | 69 | 72 | 10 | chr9_108865909_T_G_b38 | + | MODIFIER | chr9 | T | G | TogoVar |
| 108861577:splice 108861577:variant goto | ACTL7Aupstream_gene_variantc.-746T>Cothers(1): Show | TMEM245 Skin_Not_Sun_Exposed_Suprapubic 3.699 0.306 | 8131515 | a0001a0002a0003a0004a0005others(3): Show | a0001c0001a0001c0010a0001c0012a0001c0013a0002c0002others(8): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003a0001c0010t0001a0001c0012t0001others(10): Show | a0001c0001t0001g0000a0001c0001t0002g0000a0001c0001t0003g0000a0001c0010t0001g0000a0001c0012t0001g0000others(10): Show | HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00280.hp1 others(475): Show |
0.976 | 30 | 31 | 10 | chr9_108861577_T_C_b38 | + | MODIFIER | chr9 | T | C | TogoVar |
| 108861577:splice 108861577:variant goto | ACTL7Aupstream_gene_variantc.-746T>Cothers(1): Show | ACTL7A Testis 3.880 -0.149 | 8131515 | a0001a0002a0003a0004a0005others(3): Show | a0001c0001a0001c0010a0001c0012a0001c0013a0002c0002others(8): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003a0001c0010t0001a0001c0012t0001others(10): Show | a0001c0001t0001g0000a0001c0001t0002g0000a0001c0001t0003g0000a0001c0010t0001g0000a0001c0012t0001g0000others(10): Show | HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00280.hp1 others(475): Show |
0.970 | 25 | 25 | 10 | chr9_108861577_T_C_b38 | + | MODIFIER | chr9 | T | C | TogoVar |
| 108861985:splice 108861985:variant goto | ACTL7Aupstream_gene_variantc.-338G>Cothers(1): Show | TMEM245 Brain_Cerebellum 4.112 -0.219 | 7121414 | a0001a0002a0003a0004a0005others(2): Show | a0001c0001a0001c0010a0001c0012a0001c0013a0002c0002others(7): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003a0001c0010t0001a0001c0012t0001others(9): Show | a0001c0001t0001g0000a0001c0001t0002g0000a0001c0001t0003g0000a0001c0010t0001g0000a0001c0012t0001g0000others(9): Show | HG00099.hp1 HG00099.hp2 HG00140.hp2 HG00280.hp1 HG00280.hp2 others(412): Show |
0.858 | 71 | 75 | 10 | chr9_108861985_G_C_b38 | + | MODIFIER | chr9 | G | C | TogoVar |
| 108861985:splice 108861985:variant goto | ACTL7Aupstream_gene_variantc.-338G>Cothers(1): Show | ELP1 Cells_EBV-transformed_lymphocytes 4.409 0.262 | 7121414 | a0001a0002a0003a0004a0005others(2): Show | a0001c0001a0001c0010a0001c0012a0001c0013a0002c0002others(7): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003a0001c0010t0001a0001c0012t0001others(9): Show | a0001c0001t0001g0000a0001c0001t0002g0000a0001c0001t0003g0000a0001c0010t0001g0000a0001c0012t0001g0000others(9): Show | HG00099.hp1 HG00099.hp2 HG00140.hp2 HG00280.hp1 HG00280.hp2 others(412): Show |
0.860 | 84 | 91 | 10 | chr9_108861985_G_C_b38 | + | MODIFIER | chr9 | G | C | TogoVar |
| 108861985:splice 108861985:variant goto | ACTL7Aupstream_gene_variantc.-338G>Cothers(1): Show | TMEM245 Lung 3.908 -0.100 | 7121414 | a0001a0002a0003a0004a0005others(2): Show | a0001c0001a0001c0010a0001c0012a0001c0013a0002c0002others(7): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003a0001c0010t0001a0001c0012t0001others(9): Show | a0001c0001t0001g0000a0001c0001t0002g0000a0001c0001t0003g0000a0001c0010t0001g0000a0001c0012t0001g0000others(9): Show | HG00099.hp1 HG00099.hp2 HG00140.hp2 HG00280.hp1 HG00280.hp2 others(412): Show |
0.864 | 153 | 164 | 10 | chr9_108861985_G_C_b38 | + | MODIFIER | chr9 | G | C | TogoVar |
| 108861985:splice 108861985:variant goto | ACTL7Aupstream_gene_variantc.-338G>Cothers(1): Show | ELP1 Muscle_Skeletal 13.526 0.267 | 7121414 | a0001a0002a0003a0004a0005others(2): Show | a0001c0001a0001c0010a0001c0012a0001c0013a0002c0002others(7): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003a0001c0010t0001a0001c0012t0001others(9): Show | a0001c0001t0001g0000a0001c0001t0002g0000a0001c0001t0003g0000a0001c0010t0001g0000a0001c0012t0001g0000others(9): Show | HG00099.hp1 HG00099.hp2 HG00140.hp2 HG00280.hp1 HG00280.hp2 others(412): Show |
0.849 | 222 | 246 | 10 | chr9_108861985_G_C_b38 | + | MODIFIER | chr9 | G | C | TogoVar |
| 108861985:splice 108861985:variant goto | ACTL7Aupstream_gene_variantc.-338G>Cothers(1): Show | CTNNAL1 Nerve_Tibial 3.632 -0.092 | 7121414 | a0001a0002a0003a0004a0005others(2): Show | a0001c0001a0001c0010a0001c0012a0001c0013a0002c0002others(7): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003a0001c0010t0001a0001c0012t0001others(9): Show | a0001c0001t0001g0000a0001c0001t0002g0000a0001c0001t0003g0000a0001c0010t0001g0000a0001c0012t0001g0000others(9): Show | HG00099.hp1 HG00099.hp2 HG00140.hp2 HG00280.hp1 HG00280.hp2 others(412): Show |
0.843 | 189 | 210 | 10 | chr9_108861985_G_C_b38 | + | MODIFIER | chr9 | G | C | TogoVar |
| 108861985:splice 108861985:variant goto | ACTL7Aupstream_gene_variantc.-338G>Cothers(1): Show | ACTL7A Testis 21.978 -0.159 | 7121414 | a0001a0002a0003a0004a0005others(2): Show | a0001c0001a0001c0010a0001c0012a0001c0013a0002c0002others(7): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003a0001c0010t0001a0001c0012t0001others(9): Show | a0001c0001t0001g0000a0001c0001t0002g0000a0001c0001t0003g0000a0001c0010t0001g0000a0001c0012t0001g0000others(9): Show | HG00099.hp1 HG00099.hp2 HG00140.hp2 HG00280.hp1 HG00280.hp2 others(412): Show |
0.828 | 128 | 142 | 10 | chr9_108861985_G_C_b38 | + | MODIFIER | chr9 | G | C | TogoVar |
| 108861985:splice 108861985:variant goto | ACTL7Aupstream_gene_variantc.-338G>Cothers(1): Show | ELP1 Testis 4.953 0.110 | 7121414 | a0001a0002a0003a0004a0005others(2): Show | a0001c0001a0001c0010a0001c0012a0001c0013a0002c0002others(7): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003a0001c0010t0001a0001c0012t0001others(9): Show | a0001c0001t0001g0000a0001c0001t0002g0000a0001c0001t0003g0000a0001c0010t0001g0000a0001c0012t0001g0000others(9): Show | HG00099.hp1 HG00099.hp2 HG00140.hp2 HG00280.hp1 HG00280.hp2 others(412): Show |
0.828 | 128 | 142 | 10 | chr9_108861985_G_C_b38 | + | MODIFIER | chr9 | G | C | TogoVar |
| 108861985:splice 108861985:variant goto | ACTL7Aupstream_gene_variantc.-338G>Cothers(1): Show | ELP1 Whole_Blood 4.533 0.102 | 7121414 | a0001a0002a0003a0004a0005others(2): Show | a0001c0001a0001c0010a0001c0012a0001c0013a0002c0002others(7): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003a0001c0010t0001a0001c0012t0001others(9): Show | a0001c0001t0001g0000a0001c0001t0002g0000a0001c0001t0003g0000a0001c0010t0001g0000a0001c0012t0001g0000others(9): Show | HG00099.hp1 HG00099.hp2 HG00140.hp2 HG00280.hp1 HG00280.hp2 others(412): Show |
0.854 | 214 | 234 | 10 | chr9_108861985_G_C_b38 | + | MODIFIER | chr9 | G | C | TogoVar |
| 108858448:splice 108858448:variant goto | ACTL7Aupstream_gene_variantc.-3875G>Aothers(2): Show | TMEM245 Brain_Putamen_basal_ganglia 4.169 -0.158 | 4688 | a0001a0002a0004a0008 | a0001c0001a0001c0010a0001c0012a0002c0004a0004c0005others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003a0001c0010t0001a0001c0012t0001others(3): Show | a0001c0001t0001g0000a0001c0001t0002g0000a0001c0001t0003g0000a0001c0010t0001g0000a0001c0012t0001g0000others(3): Show | HG00280.hp1 HG00323.hp2 HG00408.hp1 HG00438.hp2 HG00558.hp1 others(140): Show |
0.324 | 139 | 164 | 10 | chr9_108858448_G_A_b38 | + | MODIFIER | chr9 | G | A | TogoVar |
| 108858448:splice 108858448:variant goto | ACTL7Aupstream_gene_variantc.-3875G>Aothers(2): Show | FRRS1L Breast_Mammary_Tissue 4.605 -0.203 | 4688 | a0001a0002a0004a0008 | a0001c0001a0001c0010a0001c0012a0002c0004a0004c0005others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003a0001c0010t0001a0001c0012t0001others(3): Show | a0001c0001t0001g0000a0001c0001t0002g0000a0001c0001t0003g0000a0001c0010t0001g0000a0001c0012t0001g0000others(3): Show | HG00280.hp1 HG00323.hp2 HG00408.hp1 HG00438.hp2 HG00558.hp1 others(140): Show |
0.325 | 275 | 332 | 10 | chr9_108858448_G_A_b38 | + | MODIFIER | chr9 | G | A | TogoVar |
| 108858906:splice 108858906:variant goto | ACTL7Aupstream_gene_variantc.-3417T>Cothers(2): Show | FRRS1L Breast_Mammary_Tissue 4.662 -0.204 | 4688 | a0001a0002a0004a0008 | a0001c0001a0001c0010a0001c0012a0002c0004a0004c0005others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003a0001c0010t0001a0001c0012t0001others(3): Show | a0001c0001t0001g0000a0001c0001t0002g0000a0001c0001t0003g0000a0001c0010t0001g0000a0001c0012t0001g0000others(3): Show | HG00280.hp1 HG00323.hp2 HG00408.hp1 HG00438.hp2 HG00558.hp1 others(134): Show |
0.327 | 276 | 334 | 10 | chr9_108858906_T_C_b38 | + | MODIFIER | chr9 | T | C | TogoVar |
| 108858448:splice 108858448:variant goto | ACTL7Aupstream_gene_variantc.-3875G>Aothers(2): Show | FRRS1L Esophagus_Gastroesophageal_Junction 4.017 -0.123 | 4688 | a0001a0002a0004a0008 | a0001c0001a0001c0010a0001c0012a0002c0004a0004c0005others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003a0001c0010t0001a0001c0012t0001others(3): Show | a0001c0001t0001g0000a0001c0001t0002g0000a0001c0001t0003g0000a0001c0010t0001g0000a0001c0012t0001g0000others(3): Show | HG00280.hp1 HG00323.hp2 HG00408.hp1 HG00438.hp2 HG00558.hp1 others(140): Show |
0.350 | 234 | 282 | 10 | chr9_108858448_G_A_b38 | + | MODIFIER | chr9 | G | A | TogoVar |
| 108858906:splice 108858906:variant goto | ACTL7Aupstream_gene_variantc.-3417T>Cothers(2): Show | FRRS1L Esophagus_Gastroesophageal_Junction 4.000 -0.122 | 4688 | a0001a0002a0004a0008 | a0001c0001a0001c0010a0001c0012a0002c0004a0004c0005others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003a0001c0010t0001a0001c0012t0001others(3): Show | a0001c0001t0001g0000a0001c0001t0002g0000a0001c0001t0003g0000a0001c0010t0001g0000a0001c0012t0001g0000others(3): Show | HG00280.hp1 HG00323.hp2 HG00408.hp1 HG00438.hp2 HG00558.hp1 others(134): Show |
0.347 | 233 | 280 | 10 | chr9_108858906_T_C_b38 | + | MODIFIER | chr9 | T | C | TogoVar |
| 108858448:splice 108858448:variant goto | ACTL7Aupstream_gene_variantc.-3875G>Aothers(2): Show | ELP1 Skin_Not_Sun_Exposed_Suprapubic 3.886 -0.099 | 4688 | a0001a0002a0004a0008 | a0001c0001a0001c0010a0001c0012a0002c0004a0004c0005others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003a0001c0010t0001a0001c0012t0001others(3): Show | a0001c0001t0001g0000a0001c0001t0002g0000a0001c0001t0003g0000a0001c0010t0001g0000a0001c0012t0001g0000others(3): Show | HG00280.hp1 HG00323.hp2 HG00408.hp1 HG00438.hp2 HG00558.hp1 others(140): Show |
0.334 | 363 | 433 | 10 | chr9_108858448_G_A_b38 | + | MODIFIER | chr9 | G | A | TogoVar |
| 108858906:splice 108858906:variant goto | ACTL7Aupstream_gene_variantc.-3417T>Cothers(2): Show | ELP1 Skin_Not_Sun_Exposed_Suprapubic 4.292 -0.104 | 4688 | a0001a0002a0004a0008 | a0001c0001a0001c0010a0001c0012a0002c0004a0004c0005others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003a0001c0010t0001a0001c0012t0001others(3): Show | a0001c0001t0001g0000a0001c0001t0002g0000a0001c0001t0003g0000a0001c0010t0001g0000a0001c0012t0001g0000others(3): Show | HG00280.hp1 HG00323.hp2 HG00408.hp1 HG00438.hp2 HG00558.hp1 others(134): Show |
0.331 | 361 | 430 | 10 | chr9_108858906_T_C_b38 | + | MODIFIER | chr9 | T | C | TogoVar |
| 108867855:splice 108867855:variant goto | ACTL7Adownstream_gene_variantc.*4225G>A< others(4): Show |
TMEM245 Adipose_Subcutaneous 12.792 -0.240 | 2355 | a0001a0002 | a0001c0001a0002c0002a0002c0004 | a0001c0001t0001a0001c0001t0002a0001c0001t0003a0002c0002t0001a0002c0004t0001 | a0001c0001t0001g0000a0001c0001t0002g0000a0001c0001t0003g0000a0002c0002t0001g0000a0002c0004t0001g0000 | HG00280.hp1 HG00558.hp1 HG00639.hp2 HG01069.hp1 HG01074.hp2 others(58): Show |
0.091 | 124 | 130 | 10 | chr9_108867855_G_A_b38 | + | MODIFIER | chr9 | G | A | TogoVar |
| 108867856:splice 108867856:variant goto | ACTL7Adownstream_gene_variantc.*4226G>C< others(4): Show |
TMEM245 Adipose_Subcutaneous 12.792 -0.240 | 2355 | a0001a0002 | a0001c0001a0002c0002a0002c0004 | a0001c0001t0001a0001c0001t0002a0001c0001t0003a0002c0002t0001a0002c0004t0001 | a0001c0001t0001g0000a0001c0001t0002g0000a0001c0001t0003g0000a0002c0002t0001g0000a0002c0004t0001g0000 | HG00280.hp1 HG00558.hp1 HG00639.hp2 HG01069.hp1 HG01074.hp2 others(58): Show |
0.091 | 124 | 130 | 10 | chr9_108867856_G_C_b38 | + | MODIFIER | chr9 | G | C | TogoVar |
| 108867855:splice 108867855:variant goto | ACTL7Adownstream_gene_variantc.*4225G>A< others(4): Show |
TMEM245 Artery_Tibial 13.937 -0.290 | 2355 | a0001a0002 | a0001c0001a0002c0002a0002c0004 | a0001c0001t0001a0001c0001t0002a0001c0001t0003a0002c0002t0001a0002c0004t0001 | a0001c0001t0001g0000a0001c0001t0002g0000a0001c0001t0003g0000a0002c0002t0001g0000a0002c0004t0001g0000 | HG00280.hp1 HG00558.hp1 HG00639.hp2 HG01069.hp1 HG01074.hp2 others(58): Show |
0.087 | 114 | 120 | 10 | chr9_108867855_G_A_b38 | + | MODIFIER | chr9 | G | A | TogoVar |
| 108867856:splice 108867856:variant goto | ACTL7Adownstream_gene_variantc.*4226G>C< others(4): Show |
TMEM245 Artery_Tibial 13.937 -0.290 | 2355 | a0001a0002 | a0001c0001a0002c0002a0002c0004 | a0001c0001t0001a0001c0001t0002a0001c0001t0003a0002c0002t0001a0002c0004t0001 | a0001c0001t0001g0000a0001c0001t0002g0000a0001c0001t0003g0000a0002c0002t0001g0000a0002c0004t0001g0000 | HG00280.hp1 HG00558.hp1 HG00639.hp2 HG01069.hp1 HG01074.hp2 others(58): Show |
0.087 | 114 | 120 | 10 | chr9_108867856_G_C_b38 | + | MODIFIER | chr9 | G | C | TogoVar |
| 108867855:splice 108867855:variant goto | ACTL7Adownstream_gene_variantc.*4225G>A< others(4): Show |
TMEM245 Brain_Caudate_basal_ganglia 4.040 -0.204 | 2355 | a0001a0002 | a0001c0001a0002c0002a0002c0004 | a0001c0001t0001a0001c0001t0002a0001c0001t0003a0002c0002t0001a0002c0004t0001 | a0001c0001t0001g0000a0001c0001t0002g0000a0001c0001t0003g0000a0002c0002t0001g0000a0002c0004t0001g0000 | HG00280.hp1 HG00558.hp1 HG00639.hp2 HG01069.hp1 HG01074.hp2 others(58): Show |
0.091 | 50 | 54 | 10 | chr9_108867855_G_A_b38 | + | MODIFIER | chr9 | G | A | TogoVar |
| 108867856:splice 108867856:variant goto | ACTL7Adownstream_gene_variantc.*4226G>C< others(4): Show |
TMEM245 Brain_Caudate_basal_ganglia 4.040 -0.204 | 2355 | a0001a0002 | a0001c0001a0002c0002a0002c0004 | a0001c0001t0001a0001c0001t0002a0001c0001t0003a0002c0002t0001a0002c0004t0001 | a0001c0001t0001g0000a0001c0001t0002g0000a0001c0001t0003g0000a0002c0002t0001g0000a0002c0004t0001g0000 | HG00280.hp1 HG00558.hp1 HG00639.hp2 HG01069.hp1 HG01074.hp2 others(58): Show |
0.091 | 50 | 54 | 10 | chr9_108867856_G_C_b38 | + | MODIFIER | chr9 | G | C | TogoVar |
| 108867855:splice 108867855:variant goto | ACTL7Adownstream_gene_variantc.*4225G>A< others(4): Show |
TMEM245 Breast_Mammary_Tissue 9.715 -0.210 | 2355 | a0001a0002 | a0001c0001a0002c0002a0002c0004 | a0001c0001t0001a0001c0001t0002a0001c0001t0003a0002c0002t0001a0002c0004t0001 | a0001c0001t0001g0000a0001c0001t0002g0000a0001c0001t0003g0000a0002c0002t0001g0000a0002c0004t0001g0000 | HG00280.hp1 HG00558.hp1 HG00639.hp2 HG01069.hp1 HG01074.hp2 others(58): Show |
0.085 | 83 | 87 | 10 | chr9_108867855_G_A_b38 | + | MODIFIER | chr9 | G | A | TogoVar |
| 108867856:splice 108867856:variant goto | ACTL7Adownstream_gene_variantc.*4226G>C< others(4): Show |
TMEM245 Breast_Mammary_Tissue 9.715 -0.210 | 2355 | a0001a0002 | a0001c0001a0002c0002a0002c0004 | a0001c0001t0001a0001c0001t0002a0001c0001t0003a0002c0002t0001a0002c0004t0001 | a0001c0001t0001g0000a0001c0001t0002g0000a0001c0001t0003g0000a0002c0002t0001g0000a0002c0004t0001g0000 | HG00280.hp1 HG00558.hp1 HG00639.hp2 HG01069.hp1 HG01074.hp2 others(58): Show |
0.085 | 83 | 87 | 10 | chr9_108867856_G_C_b38 | + | MODIFIER | chr9 | G | C | TogoVar |