| geneid | 10157 |
|---|---|
| ensemblid | ENSG00000008311.16 |
| hgncid | 17366 |
| symbol | AASS |
| name | aminoadipate-semialdehyde synthase |
| refseq_nuc | NM_005763.4 |
| refseq_prot | NP_005754.2 |
| ensembl_nuc | ENST00000417368.7 |
| ensembl_prot | ENSP00000403768.2 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 122073549 |
| end | 122144249 |
| strand | - |
| ver | v1.2 |
| region | chr7:122073549-122144249 |
| region5000 | chr7:122068549-122149249 |
| regionname0 | AASS_chr7_122073549_122144249 |
| regionname5000 | AASS_chr7_122068549_122149249 |
| 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 |
|---|
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| AASS | 1/1 | a0001 | 926 | 368 | 81 | 74 | 164 | 11 | 36 | subcellular location copy fasta | chr7 | 122068549 | 122149249 |
| 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
|
chapid | clen | total | AFR | AMR | EAS | EUR | SAS | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| AASS | 1/1 | c0001 | 2781 | 363 | 78 | 74 | 164 | 10 | 35 | copy fasta | chr7 | 122068549 | 122149249 |
| genename | grch38/chm13v2 | thapid | tlen | total | AFR | AMR | EAS | EUR | SAS | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| AASS | 1/0 | t0002 | 3045 | 99 | 4 | 23 | 52 | 6 | 13 | copy fasta | chr7 | 122068549 | 122149249 |
| 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 |
achapid | total | AFR | AMR | EAS | EUR | SAS | clen | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| AASS | 1/1 | a0001c0001 | 363 | 78 | 74 | 164 | 10 | 35 | 2781 | copy fasta | chr7 | 122068549 | 122149249 |
| 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 |
acthapid | total | AFR | AMR | EAS | EUR | SAS | tlen | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| AASS | 1/0 | a0001c0001t0002 | 98 | 4 | 23 | 51 | 6 | 13 | 5825 | copy fasta | chr7 | 122068549 | 122149249 |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 122144161 | - | 1 | -0.9130 | -0.9061 | -0.9060 | 0.0070 | acceptor | a0001c0001t0002 | HG00735.hp2 | HG02080.hp2 HG04204.hp1 NA18955.hp1 NA18992.hp2 NA19062.hp1 |
AASS | chr7 | 122068549 | 122149249 |
| 122133517 | - | 2 | -0.9959 | -0.9957 | -0.9956 | 0.0003 | acceptor | a0001c0001t0002 | homoSapiens_grch38.hp1 | NA18979.hp1 | AASS | chr7 | 122068549 | 122149249 |
| 122133741 | - | 2 | 0.9859 | 0.9857 | 0.9855 | 0.0004 | donor | a0001c0001t0002 | HG04204.hp1 | HG01099.hp1 | AASS | chr7 | 122068549 | 122149249 |
| 122129361 | - | 3 | -0.9864 | -0.9862 | -0.9800 | 0.0064 | acceptor | a0001c0001t0002 | HG01975.hp1 | HG01099.hp1 | AASS | chr7 | 122068549 | 122149249 |
| 122129537 | - | 3 | 0.9763 | 0.9725 | 0.9719 | 0.0044 | donor | a0001c0001t0002 | HG01099.hp1 | HG02572.hp1 | AASS | chr7 | 122068549 | 122149249 |
| 122126375 | - | 4 | -0.9977 | -0.9977 | -0.9977 | 0.0000 | acceptor | a0001c0001t0002 | HG00741.hp2 HG01099.hp1 HG02572.hp1 NA20805.hp2 |
HG01975.hp1 HG02735.hp2 |
AASS | chr7 | 122068549 | 122149249 |
| 122126459 | - | 4 | 0.9980 | 0.9979 | 0.9979 | 0.0000 | donor | a0001c0001t0002 | HG01975.hp1 | HG00741.hp2 HG01099.hp1 HG02735.hp2 |
AASS | chr7 | 122068549 | 122149249 |
| 122118563 | - | 5 | -0.9849 | -0.9840 | -0.9837 | 0.0012 | acceptor | a0001c0001t0002 | NA19079.hp2 | HG02602.hp2 | AASS | chr7 | 122068549 | 122149249 |
| 122118630 | - | 5 | 0.9870 | 0.9862 | 0.9860 | 0.0010 | donor | a0001c0001t0002 | HG02040.hp1 | HG00735.hp2 HG01884.hp1 |
AASS | chr7 | 122068549 | 122149249 |
| 122118307 | - | 6 | -0.9743 | -0.9739 | -0.9736 | 0.0007 | acceptor | a0001c0001t0002 | HG02040.hp1 | NA18967.hp2 | AASS | chr7 | 122068549 | 122149249 |
| 122118453 | - | 6 | 0.9857 | 0.9855 | 0.9852 | 0.0005 | donor | a0001c0001t0002 | HG02040.hp1 | NA18967.hp2 | AASS | chr7 | 122068549 | 122149249 |
| 122116879 | - | 7 | -0.9953 | -0.9953 | -0.9952 | 0.0001 | acceptor | a0001c0001t0002 | HG02040.hp1 | HG02602.hp2 | AASS | chr7 | 122068549 | 122149249 |
| 122116957 | - | 7 | 0.9975 | 0.9975 | 0.9974 | 0.0001 | donor | a0001c0001t0002 | NA18967.hp2 | HG02040.hp1 HG02602.hp2 |
AASS | chr7 | 122068549 | 122149249 |
| 122116633 | - | 8 | -0.9995 | -0.9995 | -0.9995 | 0.0000 | acceptor | a0001c0001t0002 | HG01258.hp2 | HG02040.hp1 HG02602.hp2 NA18950.hp2 NA18967.hp2 NA19054.hp2 others(3): Show |
AASS | chr7 | 122068549 | 122149249 |
| 122116760 | - | 8 | 0.9989 | 0.9989 | 0.9989 | 0.0000 | donor | a0001c0001t0002 | HG00741.hp2 HG01099.hp1 HG02040.hp1 HG02572.hp1 NA18967.hp2 others(3): Show |
HG01258.hp2 | AASS | chr7 | 122068549 | 122149249 |
| 122115074 | - | 9 | -0.9383 | -0.9348 | -0.9330 | 0.0054 | acceptor | a0001c0001t0002 | HG01258.hp2 | HG00741.hp2 HG01099.hp1 |
AASS | chr7 | 122068549 | 122149249 |
| 122115222 | - | 9 | 0.9563 | 0.9548 | 0.9545 | 0.0019 | donor | a0001c0001t0002 | HG01258.hp2 | HG02559.hp2 | AASS | chr7 | 122068549 | 122149249 |
| 122113598 | - | 10 | -0.9921 | -0.9920 | -0.9919 | 0.0001 | acceptor | a0001c0001t0002 | HG01175.hp2 | HG02559.hp2 | AASS | chr7 | 122068549 | 122149249 |
| 122113720 | - | 10 | 0.9810 | 0.9808 | 0.9790 | 0.0019 | donor | a0001c0001t0002 | NA19054.hp2 NA19056.hp2 NA19085.hp2 |
HG01258.hp2 | AASS | chr7 | 122068549 | 122149249 |
| 122113118 | - | 11 | -0.9952 | -0.9944 | -0.9943 | 0.0008 | acceptor | a0001c0001t0002 | HG01258.hp2 | NA19054.hp2 | AASS | chr7 | 122068549 | 122149249 |
| 122113229 | - | 11 | 0.9820 | 0.9815 | 0.9814 | 0.0006 | donor | a0001c0001t0002 | HG01258.hp2 | HG02602.hp2 | AASS | chr7 | 122068549 | 122149249 |
| 122101621 | - | 12 | -0.9842 | -0.9834 | -0.9802 | 0.0040 | acceptor | a0001c0001t0002 | HG00099.hp1 | HG01099.hp1 HG01346.hp2 HG02602.hp1 HG03017.hp1 NA19087.hp2 |
AASS | chr7 | 122068549 | 122149249 |
| 122101680 | - | 12 | 0.9941 | 0.9937 | 0.9933 | 0.0008 | donor | a0001c0001t0002 | HG01099.hp1 HG01346.hp2 HG02602.hp1 HG03017.hp1 NA19087.hp2 |
HG02083.hp2 HG02129.hp1 |
AASS | chr7 | 122068549 | 122149249 |
| 122101371 | - | 13 | -0.9924 | -0.9916 | -0.9887 | 0.0037 | acceptor | a0001c0001t0002 | HG00099.hp1 | HG01099.hp1 HG01346.hp2 HG02602.hp1 HG03017.hp1 NA19087.hp2 |
AASS | chr7 | 122068549 | 122149249 |
| 122101438 | - | 13 | 0.9406 | 0.9326 | 0.9270 | 0.0136 | donor | a0001c0001t0002 | HG01175.hp2 HG02145.hp1 NA18955.hp1 |
HG02083.hp2 HG02129.hp1 |
AASS | chr7 | 122068549 | 122149249 |
| 122098745 | - | 14 | -0.7421 | -0.7047 | -0.6882 | 0.0539 | acceptor | a0001c0001t0002 | HG01099.hp1 HG01169.hp1 HG01346.hp2 HG02602.hp1 HG03017.hp1 others(1): Show |
HG01175.hp2 HG02145.hp1 NA18955.hp1 |
AASS | chr7 | 122068549 | 122149249 |
| 122098866 | - | 14 | 0.8576 | 0.8571 | 0.7949 | 0.0627 | donor | a0001c0001t0002 | NA18943.hp1 NA18954.hp2 NA18967.hp2 NA18983.hp1 NA18985.hp2 others(1): Show |
HG01175.hp2 HG02145.hp1 NA18955.hp1 |
AASS | chr7 | 122068549 | 122149249 |
| 122098450 | - | 15 | -0.9954 | -0.9941 | -0.9940 | 0.0013 | acceptor | a0001c0001t0002 | HG01099.hp1 HG01169.hp1 HG01346.hp2 HG02602.hp1 HG03017.hp1 others(1): Show |
HG00621.hp1 | AASS | chr7 | 122068549 | 122149249 |
| 122098576 | - | 15 | 0.9851 | 0.9835 | 0.9808 | 0.0044 | donor | a0001c0001t0002 | HG01175.hp2 HG02145.hp1 NA18955.hp1 |
HG01099.hp1 HG01169.hp1 HG01346.hp2 HG02602.hp1 HG03017.hp1 others(1): Show |
AASS | chr7 | 122068549 | 122149249 |
| 122093048 | - | 16 | -0.9649 | -0.9643 | -0.9634 | 0.0015 | acceptor | a0001c0001t0002 | HG00423.hp1 | HG02300.hp1 | AASS | chr7 | 122068549 | 122149249 |
| 122093158 | - | 16 | 0.9833 | 0.9827 | 0.9823 | 0.0010 | donor | a0001c0001t0002 | HG00423.hp1 | HG02683.hp1 HG03927.hp1 |
AASS | chr7 | 122068549 | 122149249 |
| 122092843 | - | 17 | -0.9755 | -0.9747 | -0.9743 | 0.0013 | acceptor | a0001c0001t0002 | NA18973.hp2 | HG02300.hp1 | AASS | chr7 | 122068549 | 122149249 |
| 122092951 | - | 17 | 0.9847 | 0.9843 | 0.9837 | 0.0010 | donor | a0001c0001t0002 | HG00423.hp1 | HG02300.hp1 | AASS | chr7 | 122068549 | 122149249 |
| 122091703 | - | 18 | -0.9432 | -0.9419 | -0.9389 | 0.0043 | acceptor | a0001c0001t0002 | NA18973.hp2 | HG00423.hp1 | AASS | chr7 | 122068549 | 122149249 |
| 122091843 | - | 18 | 0.9349 | 0.9343 | 0.9321 | 0.0027 | donor | a0001c0001t0002 | HG02300.hp1 | HG00423.hp1 | AASS | chr7 | 122068549 | 122149249 |
| 122086012 | - | 19 | -0.9983 | -0.9982 | -0.9982 | 0.0000 | acceptor | a0001c0001t0002 | HG00621.hp1 HG02683.hp1 HG03927.hp1 |
HG02735.hp2 | AASS | chr7 | 122068549 | 122149249 |
| 122086179 | - | 19 | 0.9110 | 0.9103 | 0.9093 | 0.0017 | donor | a0001c0001t0002 | NA18946.hp2 | HG02735.hp2 | AASS | chr7 | 122068549 | 122149249 |
| 122081500 | - | 20 | -0.9360 | -0.9354 | -0.7215 | 0.2145 | acceptor | a0001c0001t0002 | HG02155.hp2 NA18953.hp2 NA18971.hp1 NA18995.hp2 |
HG03669.hp2 | AASS | chr7 | 122068549 | 122149249 |
| 122081595 | - | 20 | 0.8303 | 0.8295 | 0.5648 | 0.2655 | donor | a0001c0001t0002 | HG02155.hp2 NA18953.hp2 NA18971.hp1 NA18995.hp2 |
HG03669.hp2 | AASS | chr7 | 122068549 | 122149249 |
| 122079597 | - | 21 | -0.9970 | -0.9969 | -0.9961 | 0.0009 | acceptor | a0001c0001t0002 | HG01346.hp2 | HG03669.hp2 | AASS | chr7 | 122068549 | 122149249 |
| 122079712 | - | 21 | 0.9964 | 0.9964 | 0.9954 | 0.0010 | donor | a0001c0001t0002 | NA18949.hp1 | HG03669.hp2 | AASS | chr7 | 122068549 | 122149249 |
| 122078862 | - | 22 | -0.9076 | -0.9013 | -0.8941 | 0.0135 | acceptor | a0001c0001t0002 | HG03017.hp1 NA18970.hp2 NA19010.hp2 NA19087.hp2 |
HG03669.hp2 | AASS | chr7 | 122068549 | 122149249 |
| 122078950 | - | 22 | 0.7282 | 0.7255 | 0.7096 | 0.0187 | donor | a0001c0001t0002 | HG01346.hp2 | HG03669.hp2 | AASS | chr7 | 122068549 | 122149249 |
| 122077838 | - | 23 | -0.9991 | -0.9990 | -0.9990 | 0.0000 | acceptor | a0001c0001t0002 | HG04228.hp2 | HG02083.hp2 | AASS | chr7 | 122068549 | 122149249 |
| 122078014 | - | 23 | 0.9992 | 0.9992 | 0.9992 | 0.0000 | donor | a0001c0001t0002 | HG03017.hp1 NA18970.hp2 NA19010.hp2 NA19087.hp2 |
HG02602.hp1 HG03669.hp2 |
AASS | chr7 | 122068549 | 122149249 |
| 122076607 | - | 24 | 0.9440 | 0.9422 | 0.9410 | 0.0030 | donor | a0001c0001t0002 | NA18943.hp1 NA18954.hp2 NA18967.hp2 NA18983.hp1 NA18985.hp2 others(1): Show |
HG02083.hp2 | AASS | chr7 | 122068549 | 122149249 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 122098872:splice 122098872:variant goto | c.1407-7dupT | 1287462 | Benign | AASS:10157 | SO:0001627 intron_variant |
MedGen:CN169374|MedGen:C3661900 | - | 5 | 6 | 18 | 87 | a0001a0005a0006a0010a0011 | a0001c0001a0001c0003a0005c0007a0006c0012a0010c0011others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003a0001c0001t0004a0001c0001t0005others(13): Show | a0001c0001t0001g0030a0001c0001t0001g0035a0001c0001t0001g0043a0001c0001t0001g0047a0001c0001t0001g0048others(82): Show | HG00423.hp2 HG00609.hp2 HG00639.hp1 HG00642.hp1 HG00673.hp2 others(90): Show |
LOW | chr7 | T | TA | TogoVar |
| 122113923:splice 122113923:variant goto | c.1044-204dupT | 1273910 | Benign | AASS:10157 | SO:0001627 intron_variant |
MedGen:C3661900 | - | 2 | 4 | 7 | 16 | a0001a0009 | a0001c0001a0001c0003a0001c0014a0009c0010 | a0001c0001t0001a0001c0001t0002a0001c0001t0003a0001c0001t0007a0001c0003t0010others(2): Show | a0001c0001t0001g0030a0001c0001t0001g0035a0001c0001t0001g0117a0001c0001t0001g0221a0001c0001t0001g0315others(11): Show | HG00099.hp2 HG00323.hp2 HG00597.hp2 HG00639.hp1 HG01258.hp2 others(13): Show |
MODIFIER | chr7 | C | CA | TogoVar |
| 122098872:splice 122098872:variant goto | c.1407-7delT | 559313 | Benign | AASS:10157 | SO:0001627 intron_variant |
MedGen:CN517202 | - | 3 | 3 | 6 | 16 | a0001a0003a0009 | a0001c0001a0003c0004a0009c0010 | a0001c0001t0001a0001c0001t0002a0001c0001t0004a0001c0001t0006a0003c0004t0001others(1): Show | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0092a0001c0001t0001g0101a0001c0001t0001g0104others(11): Show | HG00323.hp2 HG01099.hp1 HG01168.hp2 HG01169.hp1 HG01346.hp2 others(12): Show |
LOW | chr7 | TA | T | TogoVar |
| 122114904:splice 122114904:variant goto | c.1043+170T>A | 1276060 | Benign | AASS:10157 | SO:0001627 intron_variant |
MedGen:C3661900 | - | 1 | 1 | 4 | 6 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003a0001c0001t0024 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0002g0189a0001c0001t0002g0218a0001c0001t0003g0304others(1): Show | HG00741.hp2 HG01099.hp1 HG02738.hp1 HG03654.hp1 NA18997.hp2 others(1): Show |
MODIFIER | chr7 | A | T | TogoVar |
| 122081605:splice 122081605:variant goto | c.2185-10C>A | 1631543 | Benign | AASS:10157 | SO:0001627 intron_variant |
MedGen:C3661900 | - | 1 | 1 | 1 | 1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0200 | HG03669.hp2 | MODIFIER | chr7 | G | T | TogoVar |
| 122101357:splice 122101357:variant goto | c.1406+14A>C | 3021451 | Benign | AASS:10157 | SO:0001627 intron_variant |
MedGen:C3661900 | - | 1 | 1 | 1 | 2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0216a0001c0001t0002g0242 | HG00423.hp1 NA18946.hp2 |
MODIFIER | chr7 | T | G | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
chr7:122114904
|
c.1043+170T>A |
Color vision defects (Deutan-Protan)0.15 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003a0001c0001t0024 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0002g0189a0001c0001t0002g0218a0001c0001t0003g0304others(1): Show | HG00741.hp2 HG01099.hp1 HG02738.hp1 HG03654.hp1 NA18997.hp2 others(1): Show |
Identifying missing pieces in color vision defects others(59): Show |
31 Silk Road (founder/genetic isolate) cases, 483 others(45): Show |
AASS | rs56052527-T | - | MODIFIER | chr7 | A | T | |
|
chr7:122145922
|
c.-1777A>G | Memory decline x sex interaction0.010824 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0110a0001c0001t0002g0001a0001c0001t0002g0190a0001c0001t0002g0195a0001c0001t0002g0203others(6): Show | HG00099.hp1 HG00280.hp2 HG00642.hp2 HG00733.hp1 HG00735.hp2 others(7): Show |
Sex-specific genetic architecture of late-life mem others(16): Show |
24,216 European ancestry individuals, 3,367 Africa others(23): Show |
AASS - RPL31P37 | rs62472936-? | - | MODIFIER | chr7 | T | C |