Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 57679 |
| ensemblid | ENSG00000003393.16 |
| hgncid | 443 |
| symbol | ALS2 |
| name | alsin Rho guanine nucleotide exchange factor ALS2 |
| refseq_nuc | NM_020919.4 |
| refseq_prot | NP_065970.2 |
| ensembl_nuc | ENST00000264276.11 |
| ensembl_prot | ENSP00000264276.6 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 201700267 |
| end | 201780933 |
| strand | - |
| ver | v1.2 |
| region | chr2:201700267-201780933 |
| region5000 | chr2:201695267-201785933 |
| regionname0 | ALS2_chr2_201700267_201780933 |
| regionname5000 | ALS2_chr2_201695267_201785933 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 1657 | 311 | 57 | 49 | 155 | 13 | 36 | 121 | ALS2_chr2_201695267_201785933 | ALS2 | MDSKK others(1652): Show |
chr2 | 201695267 | 201785933 |
| a0002 | 1/0 | 1657 | 19 | 13 | 3 | 0 | 1 | 1 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | MDSKK others(1652): Show |
chr2 | 201695267 | 201785933 |
| a0003 | 0/0 | 1657 | 6 | 4 | 1 | 0 | 0 | 1 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | MDSKK others(1652): Show |
chr2 | 201695267 | 201785933 |
| a0004 | 0/0 | 1657 | 4 | 0 | 4 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | MDSKK others(1652): Show |
chr2 | 201695267 | 201785933 |
| a0005 | 0/0 | 1657 | 2 | 0 | 0 | 0 | 2 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | MDSKK others(1652): Show |
chr2 | 201695267 | 201785933 |
| a0006 | 0/0 | 1657 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ALS2_chr2_201695267_201785933 | ALS2 | MDSKK others(1652): Show |
chr2 | 201695267 | 201785933 |
| a0007 | 0/0 | 1657 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ALS2_chr2_201695267_201785933 | ALS2 | MDSKK others(1652): Show |
chr2 | 201695267 | 201785933 |
| a0008 | 0/0 | 1657 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | MDSKK others(1652): Show |
chr2 | 201695267 | 201785933 |
| a0009 | 0/0 | 1657 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | MDSKK others(1652): Show |
chr2 | 201695267 | 201785933 |
| a0010 | 0/0 | 1657 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | MDSKK others(1652): Show |
chr2 | 201695267 | 201785933 |
| a0011 | 0/0 | 1657 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | MDSKK others(1652): Show |
chr2 | 201695267 | 201785933 |
| a0012 | 0/0 | 1657 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | MDSKK others(1652): Show |
chr2 | 201695267 | 201785933 |
| a0013 | 0/0 | 1657 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | MDSKK others(1652): Show |
chr2 | 201695267 | 201785933 |
| a0014 | 0/0 | 1657 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | MDSKK others(1652): Show |
chr2 | 201695267 | 201785933 |
| a0015 | 0/0 | 1657 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | MDSKK others(1652): Show |
chr2 | 201695267 | 201785933 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 4971 | 131 | 41 | 8 | 65 | 2 | 15 | ALS2_chr2_201695267_201785933 | ALS2 | ATGGA others(4966): Show |
chr2 | 201695267 | 201785933 | ||
| a0001c0002 | 0/1 | 4971 | 94 | 2 | 26 | 46 | 7 | 12 | ALS2_chr2_201695267_201785933 | ALS2 | ATGGA others(4966): Show |
chr2 | 201695267 | 201785933 | ||
| a0001c0003 | 0/0 | 4971 | 60 | 5 | 5 | 42 | 1 | 7 | ALS2_chr2_201695267_201785933 | ALS2 | ATGGA others(4966): Show |
chr2 | 201695267 | 201785933 | ||
| a0001c0004 | 0/0 | 4971 | 19 | 7 | 10 | 1 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | ATGGA others(4966): Show |
chr2 | 201695267 | 201785933 | ||
| a0001c0009 | 0/0 | 4971 | 4 | 0 | 0 | 0 | 3 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | ATGGA others(4966): Show |
chr2 | 201695267 | 201785933 | ||
| a0001c0011 | 0/0 | 4971 | 2 | 2 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | ATGGA others(4966): Show |
chr2 | 201695267 | 201785933 | ||
| a0001c0022 | 0/0 | 4971 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | ATGGA others(4966): Show |
chr2 | 201695267 | 201785933 | ||
| a0002c0005 | 0/0 | 4971 | 12 | 9 | 2 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | ATGGA others(4966): Show |
chr2 | 201695267 | 201785933 | ||
| a0002c0006 | 1/0 | 4971 | 6 | 3 | 1 | 0 | 1 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | ATGGA others(4966): Show |
chr2 | 201695267 | 201785933 | ||
| a0002c0020 | 0/0 | 4971 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | ATGGA others(4966): Show |
chr2 | 201695267 | 201785933 | ||
| a0003c0007 | 0/0 | 4971 | 6 | 4 | 1 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | ATGGA others(4966): Show |
chr2 | 201695267 | 201785933 | ||
| a0004c0008 | 0/0 | 4971 | 4 | 0 | 4 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | ATGGA others(4966): Show |
chr2 | 201695267 | 201785933 | ||
| a0005c0013 | 0/0 | 4971 | 2 | 0 | 0 | 0 | 2 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | ATGGA others(4966): Show |
chr2 | 201695267 | 201785933 | ||
| a0006c0012 | 0/0 | 4971 | 2 | 0 | 0 | 2 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | ATGGA others(4966): Show |
chr2 | 201695267 | 201785933 | ||
| a0007c0010 | 0/0 | 4971 | 2 | 0 | 0 | 2 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | ATGGA others(4966): Show |
chr2 | 201695267 | 201785933 | ||
| a0008c0021 | 0/0 | 4971 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | ATGGA others(4966): Show |
chr2 | 201695267 | 201785933 | ||
| a0009c0016 | 0/0 | 4971 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | ATGGA others(4966): Show |
chr2 | 201695267 | 201785933 | ||
| a0010c0014 | 0/0 | 4971 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | ATGGA others(4966): Show |
chr2 | 201695267 | 201785933 | ||
| a0011c0015 | 0/0 | 4971 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | ATGGA others(4966): Show |
chr2 | 201695267 | 201785933 | ||
| a0012c0023 | 0/0 | 4971 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | ATGGA others(4966): Show |
chr2 | 201695267 | 201785933 | ||
| a0013c0019 | 0/0 | 4971 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | ATGGA others(4966): Show |
chr2 | 201695267 | 201785933 | ||
| a0014c0017 | 0/0 | 4971 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | ATGGA others(4966): Show |
chr2 | 201695267 | 201785933 | ||
| a0015c0018 | 0/0 | 4971 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | ATGGA others(4966): Show |
chr2 | 201695267 | 201785933 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6675 | 117 | 30 | 6 | 65 | 2 | 14 | ALS2_chr2_201695267_201785933 | ALS2 | ACTGG others(6670): Show |
chr2 | 201695267 | 201785933 |
| a0001c0001t0003 | 0/0 | 6675 | 11 | 9 | 2 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | ACTGG others(6670): Show |
chr2 | 201695267 | 201785933 |
| a0001c0001t0006 | 0/0 | 6675 | 2 | 2 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | ACTGG others(6670): Show |
chr2 | 201695267 | 201785933 |
| a0001c0001t0008 | 0/0 | 6675 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | ACTGG others(6670): Show |
chr2 | 201695267 | 201785933 |
| a0001c0002t0001 | 0/1 | 6675 | 91 | 2 | 25 | 45 | 6 | 12 | ALS2_chr2_201695267_201785933 | ALS2 | ACTGG others(6670): Show |
chr2 | 201695267 | 201785933 |
| a0001c0002t0009 | 0/0 | 6675 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | ACTGG others(6670): Show |
chr2 | 201695267 | 201785933 |
| a0001c0002t0010 | 0/0 | 6675 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | ACTGG others(6670): Show |
chr2 | 201695267 | 201785933 |
| a0001c0002t0011 | 0/0 | 6675 | 1 | 0 | 0 | 0 | 1 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | ACTGG others(6670): Show |
chr2 | 201695267 | 201785933 |
| a0001c0003t0001 | 0/0 | 6675 | 2 | 1 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | ACTGG others(6670): Show |
chr2 | 201695267 | 201785933 |
| a0001c0003t0002 | 0/0 | 6675 | 52 | 2 | 2 | 42 | 1 | 5 | ALS2_chr2_201695267_201785933 | ALS2 | ACTGG others(6670): Show |
chr2 | 201695267 | 201785933 |
| a0001c0003t0004 | 0/0 | 6675 | 4 | 0 | 3 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | ACTGG others(6670): Show |
chr2 | 201695267 | 201785933 |
| a0001c0003t0007 | 0/0 | 6675 | 2 | 2 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | ACTGG others(6670): Show |
chr2 | 201695267 | 201785933 |
| a0001c0004t0001 | 0/0 | 6675 | 18 | 6 | 10 | 1 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | ACTGG others(6670): Show |
chr2 | 201695267 | 201785933 |
| a0001c0004t0003 | 0/0 | 6675 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | ACTGG others(6670): Show |
chr2 | 201695267 | 201785933 |
| a0001c0009t0001 | 0/0 | 6675 | 4 | 0 | 0 | 0 | 3 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | ACTGG others(6670): Show |
chr2 | 201695267 | 201785933 |
| a0001c0011t0001 | 0/0 | 6675 | 2 | 2 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | ACTGG others(6670): Show |
chr2 | 201695267 | 201785933 |
| a0001c0022t0001 | 0/0 | 6675 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | ACTGG others(6670): Show |
chr2 | 201695267 | 201785933 |
| a0002c0005t0001 | 0/0 | 6675 | 12 | 9 | 2 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | ACTGG others(6670): Show |
chr2 | 201695267 | 201785933 |
| a0002c0006t0001 | 1/0 | 6675 | 4 | 1 | 1 | 0 | 1 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | ACTGG others(6670): Show |
chr2 | 201695267 | 201785933 |
| a0002c0006t0005 | 0/0 | 6675 | 2 | 2 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | ACTGG others(6670): Show |
chr2 | 201695267 | 201785933 |
| a0002c0020t0001 | 0/0 | 6675 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | ACTGG others(6670): Show |
chr2 | 201695267 | 201785933 |
| a0003c0007t0001 | 0/0 | 6675 | 6 | 4 | 1 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | ACTGG others(6670): Show |
chr2 | 201695267 | 201785933 |
| a0004c0008t0001 | 0/0 | 6675 | 4 | 0 | 4 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | ACTGG others(6670): Show |
chr2 | 201695267 | 201785933 |
| a0005c0013t0001 | 0/0 | 6675 | 2 | 0 | 0 | 0 | 2 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | ACTGG others(6670): Show |
chr2 | 201695267 | 201785933 |
| a0006c0012t0002 | 0/0 | 6675 | 2 | 0 | 0 | 2 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | ACTGG others(6670): Show |
chr2 | 201695267 | 201785933 |
| a0007c0010t0001 | 0/0 | 6675 | 2 | 0 | 0 | 2 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | ACTGG others(6670): Show |
chr2 | 201695267 | 201785933 |
| a0008c0021t0001 | 0/0 | 6675 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | ACTGG others(6670): Show |
chr2 | 201695267 | 201785933 |
| a0009c0016t0001 | 0/0 | 6675 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | ACTGG others(6670): Show |
chr2 | 201695267 | 201785933 |
| a0010c0014t0001 | 0/0 | 6675 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | ACTGG others(6670): Show |
chr2 | 201695267 | 201785933 |
| a0011c0015t0002 | 0/0 | 6675 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | ACTGG others(6670): Show |
chr2 | 201695267 | 201785933 |
| a0012c0023t0001 | 0/0 | 6675 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | ACTGG others(6670): Show |
chr2 | 201695267 | 201785933 |
| a0013c0019t0012 | 0/0 | 6675 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | ACTGG others(6670): Show |
chr2 | 201695267 | 201785933 |
| a0014c0017t0001 | 0/0 | 6675 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | ACTGG others(6670): Show |
chr2 | 201695267 | 201785933 |
| a0015c0018t0001 | 0/0 | 6675 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | ACTGG others(6670): Show |
chr2 | 201695267 | 201785933 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 4 | 0 | 1 | 2 | 1 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0003g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0003g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0003g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0006g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0006g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0001t0008g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0007 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0008 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0051 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0009g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0010g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0002t0011g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0004g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0004g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0004g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0004g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0007g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0003t0007g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0004t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0004t0001g0006 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0004t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0004t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0004t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0004t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0004t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0004t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0004t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0004t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0004t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0004t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0004t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0004t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0004t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0004t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0004t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0009t0001g0016 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0009t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0009t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0011t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0011t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0001c0022t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0002c0005t0001g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0002c0005t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0002c0005t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0002c0005t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0002c0005t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0002c0005t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0002c0005t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0002c0005t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0002c0005t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0002c0006t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0002c0006t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0002c0006t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0002c0006t0001g0159 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0002c0006t0005g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0002c0006t0005g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0002c0020t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0003c0007t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0003c0007t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0003c0007t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0003c0007t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0003c0007t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0003c0007t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0004c0008t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0004c0008t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0004c0008t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0004c0008t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0005c0013t0001g0019 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0006c0012t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0006c0012t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0007c0010t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0007c0010t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0008c0021t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0009c0016t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0010c0014t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0011c0015t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0012c0023t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0013c0019t0012g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0014c0017t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| a0015c0018t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0006 | t0001 | g0059 | EUR | GBR | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG00140 | hp1 | a0001 | c0003 | t0002 | g0220 | EUR | GBR | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG00140 | hp2 | a0001 | c0002 | t0011 | g0102 | EUR | GBR | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG00280 | hp1 | a0001 | c0002 | t0001 | g0053 | EUR | FIN | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG00280 | hp2 | a0001 | c0009 | t0001 | g0016 | EUR | FIN | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0104 | EUR | FIN | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG00323 | hp2 | a0001 | c0009 | t0001 | g0016 | EUR | FIN | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | CHS | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG00423 | hp2 | a0001 | c0002 | t0001 | g0225 | EAS | CHS | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | CHS | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0125 | EAS | CHS | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG00544 | hp1 | a0001 | c0003 | t0002 | g0192 | EAS | CHS | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0115 | EAS | CHS | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | CHS | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | CHS | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | CHS | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG00597 | hp2 | a0001 | c0003 | t0002 | g0162 | EAS | CHS | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG00621 | hp1 | a0001 | c0003 | t0002 | g0298 | EAS | CHS | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | CHS | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG00642 | hp1 | a0001 | c0004 | t0001 | g0004 | AMR | PUR | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG00642 | hp2 | a0001 | c0004 | t0001 | g0076 | AMR | PUR | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | CHS | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG00673 | hp2 | a0008 | c0021 | t0001 | g0087 | EAS | CHS | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0303 | AMR | PUR | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG00733 | hp2 | a0001 | c0002 | t0001 | g0089 | AMR | PUR | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0133 | AMR | PUR | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG00738 | hp2 | a0001 | c0004 | t0001 | g0004 | AMR | PUR | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG00741 | hp1 | a0001 | c0003 | t0004 | g0156 | AMR | PUR | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0142 | AMR | PUR | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0223 | AMR | PUR | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01070 | hp1 | a0001 | c0004 | t0001 | g0078 | AMR | PUR | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01070 | hp2 | a0001 | c0002 | t0001 | g0152 | AMR | PUR | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0151 | AMR | PUR | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0224 | AMR | PUR | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01074 | hp1 | a0002 | c0005 | t0001 | g0068 | AMR | PUR | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0146 | AMR | PUR | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01081 | hp1 | a0002 | c0006 | t0001 | g0058 | AMR | PUR | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0121 | AMR | PUR | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0054 | AMR | PUR | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01099 | hp2 | a0001 | c0003 | t0004 | g0155 | AMR | PUR | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01109 | hp1 | a0001 | c0004 | t0001 | g0006 | AMR | PUR | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0022 | AMR | PUR | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01168 | hp1 | a0001 | c0003 | t0002 | g0174 | AMR | PUR | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01168 | hp2 | a0001 | c0002 | t0001 | g0120 | AMR | PUR | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01175 | hp1 | a0009 | c0016 | t0001 | g0130 | AMR | PUR | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01175 | hp2 | a0001 | c0003 | t0004 | g0154 | AMR | PUR | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0008 | AMR | PUR | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0126 | AMR | CLM | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01255 | hp2 | a0002 | c0005 | t0001 | g0066 | AMR | CLM | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01257 | hp1 | a0001 | c0002 | t0001 | g0109 | AMR | CLM | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01257 | hp2 | a0001 | c0004 | t0001 | g0048 | AMR | CLM | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01261 | hp1 | a0001 | c0002 | t0001 | g0111 | AMR | CLM | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01261 | hp2 | a0001 | c0004 | t0001 | g0077 | AMR | CLM | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0110 | AMR | CLM | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0150 | AMR | CLM | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01361 | hp2 | a0001 | c0004 | t0001 | g0049 | AMR | CLM | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0131 | AMR | CLM | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0232 | AMR | CLM | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0320 | AMR | CLM | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01496 | hp2 | a0003 | c0007 | t0001 | g0033 | AMR | CLM | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01515 | hp1 | a0001 | c0002 | t0001 | g0128 | EUR | IBS | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01515 | hp2 | a0005 | c0013 | t0001 | g0019 | EUR | IBS | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01517 | hp1 | a0001 | c0002 | t0001 | g0091 | EUR | IBS | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01517 | hp2 | a0005 | c0013 | t0001 | g0019 | EUR | IBS | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01884 | hp1 | a0001 | c0004 | t0001 | g0157 | AFR | ACB | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01884 | hp2 | a0010 | c0014 | t0001 | g0043 | AFR | ACB | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01934 | hp1 | a0001 | c0004 | t0001 | g0050 | AMR | PEL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0230 | AMR | PEL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01943 | hp1 | a0004 | c0008 | t0001 | g0235 | AMR | PEL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01943 | hp2 | a0001 | c0002 | t0001 | g0231 | AMR | PEL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01952 | hp1 | a0001 | c0002 | t0001 | g0107 | AMR | PEL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01952 | hp2 | a0004 | c0008 | t0001 | g0240 | AMR | PEL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01975 | hp1 | a0001 | c0003 | t0002 | g0199 | AMR | PEL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01975 | hp2 | a0001 | c0002 | t0010 | g0112 | AMR | PEL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01981 | hp1 | a0004 | c0008 | t0001 | g0236 | AMR | PEL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01981 | hp2 | a0001 | c0002 | t0001 | g0090 | AMR | PEL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02004 | hp1 | a0004 | c0008 | t0001 | g0239 | AMR | PEL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | PEL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | KHV | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0123 | EAS | KHV | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | KHV | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02027 | hp2 | a0001 | c0004 | t0001 | g0216 | EAS | KHV | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02055 | hp1 | a0002 | c0006 | t0001 | g0057 | AFR | ACB | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0031 | AFR | ACB | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | KHV | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02056 | hp2 | a0001 | c0022 | t0001 | g0124 | EAS | KHV | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | KHV | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02071 | hp2 | a0001 | c0003 | t0002 | g0175 | EAS | KHV | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02080 | hp1 | a0001 | c0003 | t0002 | g0171 | EAS | KHV | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0139 | EAS | KHV | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02083 | hp1 | a0001 | c0003 | t0002 | g0176 | EAS | KHV | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | KHV | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0039 | EAS | KHV | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02135 | hp1 | a0001 | c0003 | t0002 | g0177 | EAS | KHV | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02135 | hp2 | a0001 | c0002 | t0001 | g0307 | EAS | KHV | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02145 | hp1 | a0002 | c0005 | t0001 | g0062 | AFR | ACB | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02145 | hp2 | a0001 | c0004 | t0003 | g0029 | AFR | ACB | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02155 | hp1 | a0001 | c0003 | t0002 | g0189 | EAS | CDX | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02155 | hp2 | a0001 | c0002 | t0001 | g0103 | EAS | CDX | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02165 | hp1 | a0011 | c0015 | t0002 | g0188 | EAS | CDX | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | CDX | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02258 | hp1 | a0003 | c0007 | t0001 | g0080 | AFR | ACB | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | ACB | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02280 | hp1 | a0002 | c0020 | t0001 | g0063 | AFR | ACB | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02280 | hp2 | a0012 | c0023 | t0001 | g0035 | AFR | ACB | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02293 | hp1 | a0001 | c0002 | t0001 | g0113 | AMR | PEL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02293 | hp2 | a0001 | c0004 | t0001 | g0074 | AMR | PEL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0027 | AFR | ACB | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | ACB | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0255 | SAS | PJL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02602 | hp2 | a0001 | c0002 | t0001 | g0233 | SAS | PJL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02615 | hp1 | a0001 | c0011 | t0001 | g0321 | AFR | GWD | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02615 | hp2 | a0001 | c0004 | t0001 | g0044 | AFR | GWD | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0024 | AFR | GWD | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02622 | hp2 | a0001 | c0003 | t0007 | g0041 | AFR | GWD | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02630 | hp1 | a0002 | c0005 | t0001 | g0002 | AFR | GWD | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0219 | AFR | GWD | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02647 | hp1 | a0003 | c0007 | t0001 | g0037 | AFR | GWD | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02647 | hp2 | a0001 | c0004 | t0001 | g0075 | AFR | GWD | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02683 | hp1 | a0001 | c0003 | t0002 | g0200 | SAS | PJL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02683 | hp2 | a0001 | c0009 | t0001 | g0311 | SAS | PJL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02698 | hp1 | a0001 | c0003 | t0002 | g0122 | SAS | PJL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02698 | hp2 | a0001 | c0002 | t0001 | g0055 | SAS | PJL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | GWD | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02717 | hp2 | a0013 | c0019 | t0012 | g0082 | AFR | GWD | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | GWD | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02723 | hp2 | a0001 | c0004 | t0001 | g0006 | AFR | GWD | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0129 | SAS | PJL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0280 | SAS | PJL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0134 | SAS | PJL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02738 | hp2 | a0001 | c0003 | t0004 | g0166 | SAS | PJL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02818 | hp1 | a0002 | c0005 | t0001 | g0002 | AFR | GWD | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02818 | hp2 | a0001 | c0004 | t0001 | g0045 | AFR | GWD | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02886 | hp1 | a0001 | c0004 | t0001 | g0047 | AFR | GWD | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02886 | hp2 | a0001 | c0003 | t0002 | g0184 | AFR | GWD | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0020 | AFR | GWD | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | GWD | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02897 | hp1 | a0001 | c0011 | t0001 | g0084 | AFR | GWD | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | GWD | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | ESN | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | ESN | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0021 | AFR | ESN | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ESN | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | ESN | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | ESN | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0291 | AFR | ESN | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0030 | AFR | ESN | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG03017 | hp1 | a0003 | c0007 | t0001 | g0032 | SAS | PJL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0274 | SAS | PJL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0288 | AFR | GWD | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG03041 | hp2 | a0002 | c0006 | t0005 | g0061 | AFR | GWD | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0026 | AFR | MSL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG03098 | hp2 | a0001 | c0001 | t0006 | g0330 | AFR | MSL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG03130 | hp1 | a0001 | c0003 | t0007 | g0040 | AFR | ESN | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0301 | AFR | ESN | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0287 | AFR | ESN | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | ESN | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG03195 | hp1 | a0003 | c0007 | t0001 | g0036 | AFR | ESN | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG03195 | hp2 | a0002 | c0005 | t0001 | g0002 | AFR | ESN | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG03209 | hp1 | a0001 | c0001 | t0006 | g0331 | AFR | MSL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG03209 | hp2 | a0014 | c0017 | t0001 | g0228 | AFR | MSL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0023 | AFR | MSL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0127 | SAS | PJL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0297 | SAS | PJL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG03491 | hp1 | a0001 | c0003 | t0002 | g0009 | SAS | PJL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0302 | SAS | PJL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0052 | SAS | PJL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG03492 | hp2 | a0001 | c0003 | t0002 | g0009 | SAS | PJL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | ESN | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG03516 | hp2 | a0001 | c0003 | t0002 | g0194 | AFR | ESN | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG03540 | hp1 | a0002 | c0006 | t0005 | g0060 | AFR | GWD | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0292 | AFR | GWD | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG03579 | hp1 | a0002 | c0005 | t0001 | g0064 | AFR | MSL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | MSL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0313 | SAS | STU | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG03688 | hp2 | a0002 | c0005 | t0001 | g0056 | SAS | STU | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG03710 | hp1 | a0001 | c0004 | t0001 | g0079 | SAS | PJL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG03710 | hp2 | a0001 | c0001 | t0008 | g0279 | SAS | PJL | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0257 | SAS | BEB | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0135 | SAS | BEB | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG03834 | hp1 | a0001 | c0003 | t0002 | g0201 | SAS | BEB | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0290 | SAS | BEB | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0148 | SAS | BEB | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0247 | SAS | BEB | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG04115 | hp1 | a0001 | c0002 | t0001 | g0085 | SAS | STU | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG04115 | hp2 | a0001 | c0003 | t0001 | g0172 | SAS | STU | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0248 | SAS | BEB | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0314 | SAS | BEB | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0008 | SAS | STU | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0296 | SAS | STU | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | STU | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0282 | SAS | STU | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0226 | SAS | STU | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | STU | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | YRI | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | YRI | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18747 | hp1 | a0001 | c0003 | t0002 | g0203 | EAS | CHB | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | CHB | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18940 | hp1 | a0001 | c0003 | t0002 | g0183 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18941 | hp1 | a0001 | c0003 | t0002 | g0160 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18941 | hp2 | a0001 | c0002 | t0001 | g0099 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18942 | hp2 | a0001 | c0002 | t0001 | g0072 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18944 | hp1 | a0001 | c0002 | t0001 | g0098 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18944 | hp2 | a0001 | c0003 | t0002 | g0190 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18945 | hp1 | a0001 | c0003 | t0002 | g0178 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18949 | hp1 | a0001 | c0003 | t0002 | g0010 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18951 | hp1 | a0001 | c0002 | t0001 | g0105 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18952 | hp2 | a0001 | c0003 | t0002 | g0003 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18954 | hp1 | a0001 | c0003 | t0002 | g0003 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18954 | hp2 | a0001 | c0002 | t0001 | g0202 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18956 | hp2 | a0001 | c0003 | t0002 | g0186 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18957 | hp1 | a0001 | c0002 | t0001 | g0153 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18959 | hp1 | a0001 | c0003 | t0002 | g0187 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18959 | hp2 | a0001 | c0002 | t0001 | g0096 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18961 | hp2 | a0001 | c0002 | t0001 | g0204 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18965 | hp2 | a0015 | c0018 | t0001 | g0218 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18966 | hp2 | a0001 | c0002 | t0009 | g0136 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18967 | hp1 | a0001 | c0002 | t0001 | g0140 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18968 | hp1 | a0001 | c0002 | t0001 | g0069 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18970 | hp1 | a0001 | c0003 | t0002 | g0011 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18971 | hp1 | a0001 | c0003 | t0002 | g0197 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18973 | hp1 | a0001 | c0002 | t0001 | g0092 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18975 | hp1 | a0006 | c0012 | t0002 | g0161 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18978 | hp1 | a0001 | c0002 | t0001 | g0309 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18978 | hp2 | a0001 | c0003 | t0002 | g0179 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18979 | hp1 | a0001 | c0003 | t0002 | g0299 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18979 | hp2 | a0001 | c0002 | t0001 | g0138 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18980 | hp1 | a0001 | c0003 | t0002 | g0182 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18980 | hp2 | a0001 | c0002 | t0001 | g0116 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18981 | hp1 | a0001 | c0002 | t0001 | g0141 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18981 | hp2 | a0001 | c0003 | t0002 | g0167 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0117 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18986 | hp1 | a0001 | c0002 | t0001 | g0101 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18988 | hp2 | a0001 | c0002 | t0001 | g0094 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18991 | hp1 | a0001 | c0002 | t0001 | g0147 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18991 | hp2 | a0001 | c0003 | t0002 | g0181 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18992 | hp2 | a0001 | c0002 | t0001 | g0324 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18993 | hp2 | a0001 | c0002 | t0001 | g0095 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18994 | hp2 | a0006 | c0012 | t0002 | g0164 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18995 | hp1 | a0001 | c0003 | t0002 | g0088 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18998 | hp1 | a0001 | c0002 | t0001 | g0143 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18999 | hp1 | a0001 | c0002 | t0001 | g0106 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19002 | hp2 | a0001 | c0003 | t0002 | g0168 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19003 | hp1 | a0001 | c0002 | t0001 | g0086 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19003 | hp2 | a0001 | c0003 | t0002 | g0165 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19004 | hp1 | a0001 | c0003 | t0002 | g0196 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19004 | hp2 | a0001 | c0002 | t0001 | g0114 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19005 | hp1 | a0007 | c0010 | t0001 | g0145 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19007 | hp1 | a0001 | c0002 | t0001 | g0071 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19007 | hp2 | a0001 | c0003 | t0002 | g0010 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19009 | hp1 | a0001 | c0002 | t0001 | g0093 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19010 | hp1 | a0001 | c0003 | t0002 | g0163 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | LWK | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0028 | AFR | LWK | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19043 | hp1 | a0002 | c0005 | t0001 | g0005 | AFR | LWK | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | LWK | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19054 | hp2 | a0001 | c0003 | t0002 | g0011 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19056 | hp2 | a0001 | c0003 | t0002 | g0003 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19057 | hp1 | a0007 | c0010 | t0001 | g0097 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19058 | hp2 | a0001 | c0002 | t0001 | g0119 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19060 | hp2 | a0001 | c0003 | t0002 | g0191 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19065 | hp2 | a0001 | c0003 | t0002 | g0170 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19066 | hp1 | a0001 | c0002 | t0001 | g0215 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19067 | hp1 | a0001 | c0002 | t0001 | g0070 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19067 | hp2 | a0001 | c0003 | t0002 | g0173 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19070 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19072 | hp2 | a0001 | c0003 | t0002 | g0185 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19074 | hp1 | a0001 | c0003 | t0002 | g0180 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19077 | hp2 | a0001 | c0003 | t0002 | g0195 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19078 | hp2 | a0001 | c0002 | t0001 | g0100 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19079 | hp1 | a0001 | c0002 | t0001 | g0132 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19079 | hp2 | a0001 | c0003 | t0002 | g0169 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19081 | hp2 | a0001 | c0002 | t0001 | g0073 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19085 | hp2 | a0001 | c0002 | t0001 | g0137 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19086 | hp2 | a0001 | c0002 | t0001 | g0144 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19089 | hp2 | a0001 | c0003 | t0002 | g0193 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19091 | hp1 | a0001 | c0002 | t0001 | g0118 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19091 | hp2 | a0001 | c0003 | t0002 | g0198 | EAS | JPT | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | YRI | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | YRI | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0108 | EUR | TSI | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA20752 | hp2 | a0001 | c0009 | t0001 | g0229 | EUR | TSI | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA20805 | hp1 | a0001 | c0002 | t0001 | g0007 | EUR | TSI | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0281 | EUR | TSI | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01123 | hp1 | a0001 | c0001 | t0003 | g0025 | AMR | CLM | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG01123 | hp2 | a0001 | c0002 | t0001 | g0221 | AMR | CLM | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02486 | hp1 | a0001 | c0003 | t0001 | g0042 | AFR | ACB | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02486 | hp2 | a0003 | c0007 | t0001 | g0034 | AFR | ACB | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02559 | hp1 | a0002 | c0005 | t0001 | g0005 | AFR | ACB | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | ACB | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | USA | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| HG06807 | hp2 | a0002 | c0005 | t0001 | g0067 | AFR | USA | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | USA | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA20300 | hp2 | a0002 | c0005 | t0001 | g0065 | AFR | USA | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA21309 | hp1 | a0001 | c0002 | t0001 | g0158 | AFR | LWK | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0308 | AFR | LWK | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0051 | REF | REF | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| homoSapiens | grch38p0 | a0002 | c0006 | t0001 | g0159 | REF | REF | ALS2_chr2_201695267_201785933 | ALS2 | chr2 | 201695267 | 201785933 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:201706930 | C | T | 1 | a0013 | 1 | HG02717.hp2 | missense_variant | MODERATE | c.4496G>A | p.Arg1499His | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 29/34 | 4613/6675 | 4496/4974 | 1499/1657 | chr2 | 201706930 | |||
| chr2:201718204 | G | T | 1 | a0015 | 1 | NA18965.hp2 | missense_variant | MODERATE | c.3709C>A | p.Leu1237Met | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 24/34 | 3826/6675 | 3709/4974 | 1237/1657 | chr2 | 201718204 | |||
| chr2:201723437 | C | T | 2 | a0007 a0008 |
3 | HG00673.hp2 NA19005.hp1 NA19057.hp1 |
missense_variant | MODERATE | c.3517G>A | p.Glu1173Lys | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 22/34 | 3634/6675 | 3517/4974 | 1173/1657 | chr2 | 201723437 | |||
| chr2:201726526 | C | T | 1 | a0014 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.3206G>A | p.Gly1069Glu | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 19/34 | 3323/6675 | 3206/4974 | 1069/1657 | chr2 | 201726526 | |||
| chr2:201726784 | C | T | 1 | a0009 | 1 | HG01175.hp1 | missense_variant | MODERATE | c.3062G>A | p.Ser1021Asn | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 18/34 | 3179/6675 | 3062/4974 | 1021/1657 | chr2 | 201726784 | |||
| chr2:201726800 | G | C | 1 | a0012 | 1 | HG02280.hp2 | missense_variant | MODERATE | c.3046C>G | p.Pro1016Ala | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 18/34 | 3163/6675 | 3046/4974 | 1016/1657 | chr2 | 201726800 | |||
| chr2:201727238 | G | A | 1 | a0006 | 2 | NA18975.hp1 NA18994.hp2 |
missense_variant | MODERATE | c.2953C>T | p.Leu985Phe | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 17/34 | 3070/6675 | 2953/4974 | 985/1657 | chr2 | 201727238 | |||
| chr2:201746580 | G | T | 1 | a0011 | 1 | HG02165.hp1 | missense_variant | MODERATE | c.1984C>A | p.Leu662Ile | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 9/34 | 2101/6675 | 1984/4974 | 662/1657 | chr2 | 201746580 | |||
| chr2:201749717 | C | T | 1 | a0010 | 1 | HG01884.hp2 | missense_variant | MODERATE | c.1810G>A | p.Ala604Thr | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 8/34 | 1927/6675 | 1810/4974 | 604/1657 | chr2 | 201749717 | |||
| chr2:201757758 | G | C | 1 | a0005 | 2 | HG01515.hp2 HG01517.hp2 |
missense_variant&splice_region_variant | MODERATE | c.1115C>G | p.Pro372Arg | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 5/34 | 1232/6675 | 1115/4974 | 372/1657 | chr2 | 201757758 | |||
| chr2:201760892 | C | T | 14 | a0001 a0003 a0004 others(11): Show |
334 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(331): Show |
missense_variant | MODERATE | c.1102G>A | p.Val368Met | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/34 | 1219/6675 | 1102/4974 | 368/1657 | chr2 | 201760892 | |||
| chr2:201761519 | C | T | 1 | a0004 | 4 | HG01943.hp1 HG01952.hp2 HG01981.hp1 others(1): Show |
missense_variant | MODERATE | c.475G>A | p.Glu159Lys | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/34 | 592/6675 | 475/4974 | 159/1657 | chr2 | 201761519 | |||
| chr2:201761599 | G | A | 1 | a0008 | 1 | HG00673.hp2 | missense_variant | MODERATE | c.395C>T | p.Pro132Leu | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/34 | 512/6675 | 395/4974 | 132/1657 | chr2 | 201761599 | |||
| chr2:201761714 | T | C | 2 | a0003 a0012 |
7 | HG01496.hp2 HG02258.hp1 HG02280.hp2 others(4): Show |
missense_variant | MODERATE | c.280A>G | p.Ile94Val | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/34 | 397/6675 | 280/4974 | 94/1657 | chr2 | 201761714 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:201704528 | C | T | 1 | a0001c0011 | 2 | HG02615.hp1 HG02897.hp1 |
synonymous_variant | LOW | c.4764G>A | p.Ala1588Ala | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 32/34 | 4881/6675 | 4764/4974 | 1588/1657 | chr2 | 201704528 | |||
| chr2:201709888 | G | A | 1 | a0011c0015 | 1 | HG02165.hp1 | synonymous_variant | LOW | c.4273C>T | p.Leu1425Leu | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 27/34 | 4390/6675 | 4273/4974 | 1425/1657 | chr2 | 201709888 | |||
| chr2:201711098 | G | A | 20 | a0001c0001 a0001c0002 a0001c0003 others(17): Show |
327 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(324): Show |
synonymous_variant | LOW | c.4015C>T | p.Leu1339Leu | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 26/34 | 4132/6675 | 4015/4974 | 1339/1657 | chr2 | 201711098 | |||
| chr2:201715791 | C | T | 1 | a0001c0009 | 4 | HG00280.hp2 HG00323.hp2 HG02683.hp2 others(1): Show |
synonymous_variant | LOW | c.3885G>A | p.Ala1295Ala | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/34 | 4002/6675 | 3885/4974 | 1295/1657 | chr2 | 201715791 | |||
| chr2:201728557 | G | A | 3 | a0001c0003 a0006c0012 a0011c0015 |
63 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(60): Show |
synonymous_variant | LOW | c.2796C>T | p.Ser932Ser | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 15/34 | 2913/6675 | 2796/4974 | 932/1657 | chr2 | 201728557 | |||
| chr2:201733390 | C | T | 10 | a0001c0002 a0001c0011 a0001c0022 others(7): Show |
104 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(101): Show |
synonymous_variant | LOW | c.2466G>A | p.Val822Val | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/34 | 2583/6675 | 2466/4974 | 822/1657 | chr2 | 201733390 | |||
| chr2:201761694 | G | A | 1 | a0001c0022 | 1 | HG02056.hp2 | synonymous_variant | LOW | c.300C>T | p.Ser100Ser | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/34 | 417/6675 | 300/4974 | 100/1657 | chr2 | 201761694 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:201700390 | C | T | 1 | a0001c0002t0009 | 1 | NA18966.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1461G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 34/34 | 1461 | chr2 | 201700390 | ||||||
| chr2:201700649 | G | A | 1 | a0001c0002t0010 | 1 | HG01975.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1202C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 34/34 | 1202 | chr2 | 201700649 | ||||||
| chr2:201700847 | C | T | 4 | a0001c0003t0002 a0001c0003t0004 a0006c0012t0002 others(1): Show |
59 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*1004G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 34/34 | 1004 | chr2 | 201700847 | ||||||
| chr2:201700909 | T | C | 1 | a0001c0002t0011 | 1 | HG00140.hp2 | 3_prime_UTR_variant | MODIFIER | c.*942A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 34/34 | 942 | chr2 | 201700909 | ||||||
| chr2:201700958 | G | A | 3 | a0001c0003t0002 a0006c0012t0002 a0011c0015t0002 |
55 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*893C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 34/34 | 893 | chr2 | 201700958 | ||||||
| chr2:201701008 | C | T | 1 | a0001c0001t0006 | 2 | HG03098.hp2 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*843G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 34/34 | 843 | chr2 | 201701008 | ||||||
| chr2:201701073 | T | C | 1 | a0013c0019t0012 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*778A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 34/34 | 778 | chr2 | 201701073 | ||||||
| chr2:201701404 | C | T | 1 | a0002c0006t0005 | 2 | HG03041.hp2 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*447G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 34/34 | 447 | chr2 | 201701404 | ||||||
| chr2:201701472 | A | T | 1 | a0001c0003t0007 | 2 | HG02622.hp2 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*379T>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 34/34 | 379 | chr2 | 201701472 | ||||||
| chr2:201701746 | T | G | 1 | a0001c0003t0007 | 2 | HG02622.hp2 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*105A>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 34/34 | 105 | chr2 | 201701746 | ||||||
| chr2:201701836 | A | C | 1 | a0001c0001t0008 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*15T>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 34/34 | 15 | chr2 | 201701836 | ||||||
| chr2:201780911 | C | G | 2 | a0001c0001t0003 a0001c0004t0003 |
12 | HG01109.hp2 HG01123.hp1 HG02055.hp2 others(9): Show |
5_prime_UTR_variant | MODIFIER | c.-95G>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/34 | 12026 | chr2 | 201780911 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:201701972 | C | T | 1 | a0001c0001t0001g0313 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.4936-83G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 33/33 | chr2 | 201701972 | |||||||
| chr2:201702009 | C | A | 1 | a0001c0003t0002g0194 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.4936-120G>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 33/33 | chr2 | 201702009 | |||||||
| chr2:201702018 | T | C | 306 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(303): Show |
327 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(324): Show |
intron_variant | MODIFIER | c.4936-129A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 33/33 | chr2 | 201702018 | |||||||
| chr2:201702041 | C | T | 168 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(165): Show |
184 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.4936-152G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 33/33 | chr2 | 201702041 | |||||||
| chr2:201702122 | C | T | 2 | a0001c0003t0007g0040 a0001c0003t0007g0041 |
2 | HG02622.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.4936-233G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 33/33 | chr2 | 201702122 | |||||||
| chr2:201702145 | C | T | 2 | a0001c0001t0001g0275 a0001c0001t0001g0276 |
2 | NA19057.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.4936-256G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 33/33 | chr2 | 201702145 | |||||||
| chr2:201702386 | C | T | 7 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0210 others(4): Show |
7 | HG01243.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.4936-497G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 33/33 | chr2 | 201702386 | |||||||
| chr2:201702400 | G | GT | 113 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(110): Show |
124 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.4936-512dupA | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 33/33 | chr2 | 201702400 | |||||||
| chr2:201702471 | T | A | 5 | a0001c0001t0001g0260 a0003c0007t0001g0034 a0003c0007t0001g0036 others(2): Show |
5 | HG02258.hp1 HG02486.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.4936-582A>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 33/33 | chr2 | 201702471 | |||||||
| chr2:201702602 | T | A | 306 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(303): Show |
327 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(324): Show |
intron_variant | MODIFIER | c.4936-713A>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 33/33 | chr2 | 201702602 | |||||||
| chr2:201702682 | C | T | 306 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(303): Show |
327 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(324): Show |
intron_variant | MODIFIER | c.4936-793G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 33/33 | chr2 | 201702682 | |||||||
| chr2:201702838 | A | G | 327 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(324): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.4936-949T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 33/33 | chr2 | 201702838 | |||||||
| chr2:201702868 | C | A | 1 | a0001c0001t0001g0238 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.4936-979G>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 33/33 | chr2 | 201702868 | |||||||
| chr2:201702887 | G | A | 8 | a0001c0001t0001g0083 a0001c0001t0001g0205 a0002c0005t0001g0005 others(5): Show |
9 | HG01074.hp1 HG01255.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.4936-998C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 33/33 | chr2 | 201702887 | |||||||
| chr2:201703169 | AG | A | 7 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0210 others(4): Show |
7 | HG01243.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.4935+952delC | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 33/33 | chr2 | 201703169 | |||||||
| chr2:201703196 | A | G | 306 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(303): Show |
327 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(324): Show |
intron_variant | MODIFIER | c.4935+926T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 33/33 | chr2 | 201703196 | |||||||
| chr2:201703466 | T | C | 7 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0210 others(4): Show |
7 | HG01243.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.4935+656A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 33/33 | chr2 | 201703466 | |||||||
| chr2:201703594 | A | T | 306 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(303): Show |
327 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(324): Show |
intron_variant | MODIFIER | c.4935+528T>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 33/33 | chr2 | 201703594 | |||||||
| chr2:201703841 | A | G | 306 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(303): Show |
327 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(324): Show |
intron_variant | MODIFIER | c.4935+281T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 33/33 | chr2 | 201703841 | |||||||
| chr2:201703895 | G | A | 2 | a0001c0004t0001g0216 a0001c0004t0003g0029 |
2 | HG02027.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.4935+227C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 33/33 | chr2 | 201703895 | |||||||
| chr2:201703896 | G | A | 5 | a0001c0001t0001g0260 a0003c0007t0001g0034 a0003c0007t0001g0036 others(2): Show |
5 | HG02258.hp1 HG02486.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.4935+226C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 33/33 | chr2 | 201703896 | |||||||
| chr2:201704053 | G | T | 1 | a0001c0001t0001g0282 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.4935+69C>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 33/33 | chr2 | 201704053 | |||||||
| chr2:201704931 | C | A | 306 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(303): Show |
327 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(324): Show |
intron_variant | MODIFIER | c.4688+208G>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 31/33 | chr2 | 201704931 | |||||||
| chr2:201705124 | C | T | 1 | a0001c0003t0001g0042 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.4688+15G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 31/33 | chr2 | 201705124 | |||||||
| chr2:201705240 | T | C | 1 | a0001c0001t0001g0245 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.4627-40A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 30/33 | chr2 | 201705240 | |||||||
| chr2:201705269 | A | T | 306 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(303): Show |
327 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(324): Show |
intron_variant | MODIFIER | c.4627-69T>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 30/33 | chr2 | 201705269 | |||||||
| chr2:201705468 | T | C | 2 | a0001c0003t0007g0040 a0001c0003t0007g0041 |
2 | HG02622.hp2 HG03130.hp1 |
splice_region_variant&intron_variant | LOW | c.4581-7A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 29/33 | chr2 | 201705468 | |||||||
| chr2:201705509 | A | G | 306 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(303): Show |
327 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(324): Show |
intron_variant | MODIFIER | c.4581-48T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 29/33 | chr2 | 201705509 | |||||||
| chr2:201705532 | G | A | 5 | a0001c0001t0001g0260 a0003c0007t0001g0034 a0003c0007t0001g0036 others(2): Show |
5 | HG02258.hp1 HG02486.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.4581-71C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 29/33 | chr2 | 201705532 | |||||||
| chr2:201705641 | G | A | 2 | a0001c0002t0001g0151 a0001c0002t0001g0152 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.4581-180C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 29/33 | chr2 | 201705641 | |||||||
| chr2:201705758 | C | T | 1 | a0001c0004t0001g0157 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.4581-297G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 29/33 | chr2 | 201705758 | |||||||
| chr2:201705765 | T | TA | 18 | a0001c0001t0001g0038 a0001c0001t0001g0083 a0001c0001t0001g0205 others(15): Show |
19 | HG01074.hp1 HG01243.hp2 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.4581-305dupT | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 29/33 | chr2 | 201705765 | |||||||
| chr2:201705903 | G | T | 327 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(324): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.4581-442C>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 29/33 | chr2 | 201705903 | |||||||
| chr2:201705906 | G | A | 1 | a0001c0003t0002g0010 | 2 | NA18949.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.4581-445C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 29/33 | chr2 | 201705906 | |||||||
| chr2:201705943 | C | T | 1 | a0001c0003t0001g0042 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.4581-482G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 29/33 | chr2 | 201705943 | |||||||
| chr2:201705948 | C | CA | 250 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(247): Show |
266 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.4581-488dupT | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 29/33 | chr2 | 201705948 | |||||||
| chr2:201705948 | C | CAA | 51 | a0001c0002t0001g0086 a0001c0003t0002g0003 a0001c0003t0002g0009 others(48): Show |
56 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.4581-489_4581-488d others(4): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 29/33 | chr2 | 201705948 | |||||||
| chr2:201706007 | G | T | 7 | a0001c0004t0001g0006 a0001c0004t0001g0074 a0001c0004t0001g0075 others(4): Show |
8 | HG00642.hp2 HG01070.hp1 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.4581-546C>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 29/33 | chr2 | 201706007 | |||||||
| chr2:201706294 | G | A | 1 | a0001c0002t0001g0090 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.4580+552C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 29/33 | chr2 | 201706294 | |||||||
| chr2:201706369 | G | A | 1 | a0001c0003t0002g0185 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.4580+477C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 29/33 | chr2 | 201706369 | |||||||
| chr2:201706393 | GA | G | 59 | a0001c0002t0001g0151 a0001c0002t0001g0152 a0001c0003t0001g0042 others(56): Show |
64 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.4580+452delT | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 29/33 | chr2 | 201706393 | |||||||
| chr2:201706393 | GAA | G | 134 | a0001c0001t0001g0038 a0001c0001t0001g0081 a0001c0001t0001g0083 others(131): Show |
139 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.4580+451_4580+452d others(4): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 29/33 | chr2 | 201706393 | |||||||
| chr2:201706527 | C | T | 1 | a0001c0001t0001g0083 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.4580+319G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 29/33 | chr2 | 201706527 | |||||||
| chr2:201706535 | T | TTATATA | 45 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(42): Show |
49 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.4580+305_4580+310d others(8): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 29/33 | chr2 | 201706535 | |||||||
| chr2:201706535 | T | TTATATAT others(1): Show |
44 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0018 others(41): Show |
50 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.4580+303_4580+310d others(10): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 29/33 | chr2 | 201706535 | |||||||
| chr2:201706535 | T | TTATATAT others(3): Show |
17 | a0001c0001t0001g0012 a0001c0001t0001g0234 a0001c0001t0001g0257 others(14): Show |
18 | HG01069.hp1 HG01496.hp1 HG02647.hp1 others(15): Show |
intron_variant | MODIFIER | c.4580+301_4580+310d others(12): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 29/33 | chr2 | 201706535 | |||||||
| chr2:201706535 | T | TTATATAT others(5): Show |
8 | a0001c0001t0001g0243 a0001c0001t0001g0246 a0001c0001t0001g0247 others(5): Show |
8 | HG02165.hp2 HG02258.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.4580+299_4580+310d others(14): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 29/33 | chr2 | 201706535 | |||||||
| chr2:201706535 | T | TTATATAT others(7): Show |
1 | a0001c0001t0001g0312 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.4580+297_4580+310d others(16): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 29/33 | chr2 | 201706535 | |||||||
| chr2:201706535 | TTA | T | 189 | a0001c0001t0001g0038 a0001c0001t0001g0081 a0001c0001t0001g0083 others(186): Show |
199 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.4580+309_4580+310d others(4): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 29/33 | chr2 | 201706535 | |||||||
| chr2:201706624 | T | C | 1 | a0001c0001t0001g0206 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.4580+222A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 29/33 | chr2 | 201706624 | |||||||
| chr2:201706824 | C | T | 1 | a0001c0003t0002g0009 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.4580+22G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 29/33 | chr2 | 201706824 | |||||||
| chr2:201706825 | G | A | 1 | a0001c0002t0010g0112 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.4580+21C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 29/33 | chr2 | 201706825 | |||||||
| chr2:201706839 | C | T | 105 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(102): Show |
116 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(113): Show |
splice_region_variant&intron_variant | LOW | c.4580+7G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 29/33 | chr2 | 201706839 | |||||||
| chr2:201707140 | G | C | 1 | a0001c0002t0001g0221 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.4404-118C>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 28/33 | chr2 | 201707140 | |||||||
| chr2:201707205 | T | G | 3 | a0001c0003t0004g0154 a0001c0003t0004g0155 a0001c0003t0004g0156 |
3 | HG00741.hp1 HG01099.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.4404-183A>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 28/33 | chr2 | 201707205 | |||||||
| chr2:201707431 | AC | A | 4 | a0001c0002t0001g0128 a0001c0002t0001g0309 a0001c0002t0001g0324 others(1): Show |
4 | HG01515.hp1 NA18978.hp1 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.4404-410delG | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 28/33 | chr2 | 201707431 | |||||||
| chr2:201707432 | C | A | 187 | a0001c0001t0001g0038 a0001c0001t0001g0081 a0001c0001t0001g0083 others(184): Show |
197 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.4404-410G>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 28/33 | chr2 | 201707432 | |||||||
| chr2:201707434 | T | A | 4 | a0001c0002t0001g0128 a0001c0002t0001g0309 a0001c0002t0001g0324 others(1): Show |
4 | HG01515.hp1 NA18978.hp1 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.4404-412A>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 28/33 | chr2 | 201707434 | |||||||
| chr2:201707457 | C | T | 103 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(100): Show |
114 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.4403+412G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 28/33 | chr2 | 201707457 | |||||||
| chr2:201707614 | G | A | 113 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(110): Show |
124 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.4403+255C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 28/33 | chr2 | 201707614 | |||||||
| chr2:201707623 | T | C | 54 | a0001c0003t0002g0003 a0001c0003t0002g0009 a0001c0003t0002g0010 others(51): Show |
59 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.4403+246A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 28/33 | chr2 | 201707623 | |||||||
| chr2:201708083 | C | G | 104 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(101): Show |
115 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.4281-92G>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 27/33 | chr2 | 201708083 | |||||||
| chr2:201708187 | G | A | 11 | a0001c0004t0001g0004 a0001c0004t0001g0044 a0001c0004t0001g0045 others(8): Show |
12 | HG00099.hp1 HG00642.hp1 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.4281-196C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 27/33 | chr2 | 201708187 | |||||||
| chr2:201708202 | C | T | 306 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(303): Show |
327 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(324): Show |
intron_variant | MODIFIER | c.4281-211G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 27/33 | chr2 | 201708202 | |||||||
| chr2:201708317 | C | G | 306 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(303): Show |
327 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(324): Show |
intron_variant | MODIFIER | c.4281-326G>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 27/33 | chr2 | 201708317 | |||||||
| chr2:201708562 | G | C | 306 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(303): Show |
327 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(324): Show |
intron_variant | MODIFIER | c.4281-571C>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 27/33 | chr2 | 201708562 | |||||||
| chr2:201708662 | A | G | 1 | a0001c0002t0001g0103 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.4281-671T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 27/33 | chr2 | 201708662 | |||||||
| chr2:201708753 | C | T | 2 | a0001c0001t0001g0081 a0001c0001t0003g0031 |
2 | HG02055.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.4281-762G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 27/33 | chr2 | 201708753 | |||||||
| chr2:201708824 | T | C | 1 | a0001c0004t0001g0157 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.4281-833A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 27/33 | chr2 | 201708824 | |||||||
| chr2:201708879 | GA | G | 306 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(303): Show |
327 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(324): Show |
intron_variant | MODIFIER | c.4281-889delT | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 27/33 | chr2 | 201708879 | |||||||
| chr2:201708892 | A | G | 1 | a0001c0002t0001g0126 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.4281-901T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 27/33 | chr2 | 201708892 | |||||||
| chr2:201708904 | A | G | 1 | a0001c0001t0001g0038 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.4281-913T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 27/33 | chr2 | 201708904 | |||||||
| chr2:201709005 | A | G | 1 | a0002c0020t0001g0063 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.4280+876T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 27/33 | chr2 | 201709005 | |||||||
| chr2:201709014 | C | T | 1 | a0013c0019t0012g0082 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.4280+867G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 27/33 | chr2 | 201709014 | |||||||
| chr2:201709156 | C | G | 54 | a0001c0003t0002g0003 a0001c0003t0002g0009 a0001c0003t0002g0010 others(51): Show |
59 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.4280+725G>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 27/33 | chr2 | 201709156 | |||||||
| chr2:201709217 | C | T | 2 | a0001c0001t0001g0222 a0001c0001t0001g0227 |
2 | HG02004.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.4280+664G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 27/33 | chr2 | 201709217 | |||||||
| chr2:201709298 | T | C | 2 | a0001c0004t0001g0216 a0001c0004t0003g0029 |
2 | HG02027.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.4280+583A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 27/33 | chr2 | 201709298 | |||||||
| chr2:201709368 | G | A | 1 | a0010c0014t0001g0043 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.4280+513C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 27/33 | chr2 | 201709368 | |||||||
| chr2:201709490 | C | T | 1 | a0001c0003t0002g0298 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.4280+391G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 27/33 | chr2 | 201709490 | |||||||
| chr2:201709524 | G | A | 306 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(303): Show |
327 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(324): Show |
intron_variant | MODIFIER | c.4280+357C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 27/33 | chr2 | 201709524 | |||||||
| chr2:201709533 | C | T | 327 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(324): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.4280+348G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 27/33 | chr2 | 201709533 | |||||||
| chr2:201709711 | C | T | 1 | a0001c0004t0001g0074 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.4280+170G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 27/33 | chr2 | 201709711 | |||||||
| chr2:201709779 | T | C | 1 | a0001c0002t0001g0135 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.4280+102A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 27/33 | chr2 | 201709779 | |||||||
| chr2:201710091 | C | A | 1 | a0001c0011t0001g0321 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.4123-53G>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 26/33 | chr2 | 201710091 | |||||||
| chr2:201710102 | C | T | 327 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(324): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.4123-64G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 26/33 | chr2 | 201710102 | |||||||
| chr2:201710133 | G | A | 1 | a0002c0005t0001g0056 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.4123-95C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 26/33 | chr2 | 201710133 | |||||||
| chr2:201710183 | A | AT | 306 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(303): Show |
327 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(324): Show |
intron_variant | MODIFIER | c.4123-146dupA | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 26/33 | chr2 | 201710183 | |||||||
| chr2:201710377 | A | G | 306 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(303): Show |
327 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(324): Show |
intron_variant | MODIFIER | c.4123-339T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 26/33 | chr2 | 201710377 | |||||||
| chr2:201710381 | G | A | 1 | a0001c0003t0001g0042 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.4123-343C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 26/33 | chr2 | 201710381 | |||||||
| chr2:201710423 | C | G | 1 | a0001c0001t0003g0021 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.4123-385G>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 26/33 | chr2 | 201710423 | |||||||
| chr2:201710433 | T | TA | 311 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(308): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.4123-396dupT | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 26/33 | chr2 | 201710433 | |||||||
| chr2:201711183 | C | T | 7 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0210 others(4): Show |
7 | HG01243.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.4005-75G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201711183 | |||||||
| chr2:201711184 | A | G | 138 | a0001c0001t0001g0038 a0001c0001t0001g0081 a0001c0001t0001g0083 others(135): Show |
143 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.4005-76T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201711184 | |||||||
| chr2:201711219 | C | T | 104 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(101): Show |
115 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.4005-111G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201711219 | |||||||
| chr2:201711235 | A | G | 2 | a0002c0006t0001g0057 a0002c0006t0001g0059 |
2 | HG00099.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.4005-127T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201711235 | |||||||
| chr2:201711242 | C | A | 51 | a0001c0003t0002g0003 a0001c0003t0002g0009 a0001c0003t0002g0010 others(48): Show |
56 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.4005-134G>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201711242 | |||||||
| chr2:201711419 | T | C | 2 | a0001c0003t0007g0040 a0001c0003t0007g0041 |
2 | HG02622.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.4005-311A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201711419 | |||||||
| chr2:201711561 | A | AG | 103 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(100): Show |
114 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.4005-454dupC | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201711561 | |||||||
| chr2:201711853 | C | T | 11 | a0001c0004t0001g0004 a0001c0004t0001g0044 a0001c0004t0001g0045 others(8): Show |
12 | HG00099.hp1 HG00642.hp1 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.4005-745G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201711853 | |||||||
| chr2:201711861 | CCTAA | C | 306 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(303): Show |
327 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(324): Show |
intron_variant | MODIFIER | c.4005-757_4005-754d others(6): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201711861 | |||||||
| chr2:201712055 | A | G | 1 | a0001c0002t0001g0111 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.4005-947T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201712055 | |||||||
| chr2:201712082 | GA | G | 5 | a0001c0001t0003g0027 a0001c0001t0003g0028 a0001c0002t0001g0008 others(2): Show |
6 | HG01243.hp1 HG02451.hp1 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.4005-975delT | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201712082 | |||||||
| chr2:201712202 | A | G | 306 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(303): Show |
327 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(324): Show |
intron_variant | MODIFIER | c.4005-1094T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201712202 | |||||||
| chr2:201712234 | C | G | 306 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(303): Show |
327 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(324): Show |
intron_variant | MODIFIER | c.4005-1126G>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201712234 | |||||||
| chr2:201712297 | T | G | 1 | a0001c0001t0001g0276 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.4005-1189A>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201712297 | |||||||
| chr2:201712413 | A | C | 306 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(303): Show |
327 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(324): Show |
intron_variant | MODIFIER | c.4005-1305T>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201712413 | |||||||
| chr2:201712578 | G | A | 109 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(106): Show |
120 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.4005-1470C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201712578 | |||||||
| chr2:201712627 | C | T | 113 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(110): Show |
124 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.4005-1519G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201712627 | |||||||
| chr2:201712718 | A | G | 3 | a0001c0002t0001g0219 a0002c0020t0001g0063 a0013c0019t0012g0082 |
3 | HG02280.hp1 HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.4005-1610T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201712718 | |||||||
| chr2:201712753 | GA | G | 168 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(165): Show |
184 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.4005-1646delT | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201712753 | |||||||
| chr2:201712770 | G | GAA | 305 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(302): Show |
325 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(322): Show |
intron_variant | MODIFIER | c.4005-1664_4005-166 others(6): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201712770 | |||||||
| chr2:201712849 | T | C | 306 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(303): Show |
327 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(324): Show |
intron_variant | MODIFIER | c.4005-1741A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201712849 | |||||||
| chr2:201712901 | T | C | 8 | a0001c0001t0001g0083 a0001c0001t0001g0205 a0002c0005t0001g0005 others(5): Show |
9 | HG01074.hp1 HG01255.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.4005-1793A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201712901 | |||||||
| chr2:201712915 | T | C | 1 | a0001c0001t0001g0258 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.4005-1807A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201712915 | |||||||
| chr2:201712942 | A | G | 306 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(303): Show |
327 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(324): Show |
intron_variant | MODIFIER | c.4005-1834T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201712942 | |||||||
| chr2:201713069 | A | G | 1 | a0001c0001t0001g0246 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.4005-1961T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201713069 | |||||||
| chr2:201713122 | C | CCTTTT | 104 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(101): Show |
114 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.4005-2019_4005-201 others(9): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201713122 | |||||||
| chr2:201713133 | C | CT | 123 | a0001c0001t0001g0038 a0001c0001t0001g0081 a0001c0001t0001g0083 others(120): Show |
128 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.4005-2026dupA | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201713133 | |||||||
| chr2:201713133 | C | CTT | 7 | a0001c0001t0003g0025 a0001c0002t0001g0055 a0001c0002t0001g0099 others(4): Show |
7 | HG01123.hp1 HG02145.hp1 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.4005-2027_4005-202 others(6): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201713133 | |||||||
| chr2:201713133 | C | CTTTTCT | 12 | a0001c0003t0007g0040 a0001c0004t0001g0004 a0001c0004t0001g0044 others(9): Show |
13 | HG00099.hp1 HG00642.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.4005-2026_4005-202 others(10): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201713133 | |||||||
| chr2:201713133 | CTTTTTTT others(5): Show |
C | 1 | a0001c0003t0001g0042 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.4005-2037_4005-202 others(16): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201713133 | |||||||
| chr2:201713137 | T | TC | 53 | a0001c0003t0002g0003 a0001c0003t0002g0009 a0001c0003t0002g0010 others(50): Show |
58 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.4005-2030_4005-202 others(5): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201713137 | |||||||
| chr2:201713138 | T | C | 108 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(105): Show |
119 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.4005-2030A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201713138 | |||||||
| chr2:201713139 | T | C | 1 | a0001c0001t0001g0268 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.4005-2031A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201713139 | |||||||
| chr2:201713208 | C | T | 1 | a0001c0001t0001g0247 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.4005-2100G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201713208 | |||||||
| chr2:201713223 | A | G | 320 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(317): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.4005-2115T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201713223 | |||||||
| chr2:201713310 | T | C | 54 | a0001c0003t0002g0003 a0001c0003t0002g0009 a0001c0003t0002g0010 others(51): Show |
59 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.4005-2202A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201713310 | |||||||
| chr2:201713397 | C | A | 3 | a0001c0002t0001g0219 a0002c0020t0001g0063 a0013c0019t0012g0082 |
3 | HG02280.hp1 HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.4004+2275G>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201713397 | |||||||
| chr2:201713404 | A | G | 306 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(303): Show |
327 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(324): Show |
intron_variant | MODIFIER | c.4004+2268T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201713404 | |||||||
| chr2:201713532 | G | A | 306 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(303): Show |
327 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(324): Show |
intron_variant | MODIFIER | c.4004+2140C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201713532 | |||||||
| chr2:201713602 | G | A | 306 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(303): Show |
327 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(324): Show |
intron_variant | MODIFIER | c.4004+2070C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201713602 | |||||||
| chr2:201713626 | G | A | 1 | a0001c0001t0001g0291 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.4004+2046C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201713626 | |||||||
| chr2:201713725 | T | C | 1 | a0001c0003t0002g0183 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.4004+1947A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201713725 | |||||||
| chr2:201713743 | GTATTT | G | 104 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(101): Show |
115 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.4004+1924_4004+192 others(9): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201713743 | |||||||
| chr2:201713791 | CTA | C | 3 | a0001c0009t0001g0016 a0001c0009t0001g0229 a0001c0009t0001g0311 |
4 | HG00280.hp2 HG00323.hp2 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.4004+1879_4004+188 others(6): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201713791 | |||||||
| chr2:201714012 | T | C | 54 | a0001c0003t0002g0003 a0001c0003t0002g0009 a0001c0003t0002g0010 others(51): Show |
59 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.4004+1660A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201714012 | |||||||
| chr2:201714309 | G | A | 113 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(110): Show |
124 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.4004+1363C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201714309 | |||||||
| chr2:201714419 | G | T | 1 | a0001c0003t0002g0194 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.4004+1253C>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201714419 | |||||||
| chr2:201714461 | A | G | 1 | a0001c0003t0001g0042 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.4004+1211T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201714461 | |||||||
| chr2:201714711 | T | C | 1 | a0001c0003t0001g0042 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.4004+961A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201714711 | |||||||
| chr2:201714878 | G | A | 2 | a0001c0002t0001g0221 a0001c0002t0001g0232 |
2 | HG01123.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.4004+794C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201714878 | |||||||
| chr2:201714925 | C | T | 111 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(108): Show |
122 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.4004+747G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201714925 | |||||||
| chr2:201714934 | C | A | 11 | a0001c0004t0001g0004 a0001c0004t0001g0044 a0001c0004t0001g0045 others(8): Show |
12 | HG00099.hp1 HG00642.hp1 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.4004+738G>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201714934 | |||||||
| chr2:201715545 | T | C | 306 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(303): Show |
327 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(324): Show |
intron_variant | MODIFIER | c.4004+127A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201715545 | |||||||
| chr2:201715605 | T | G | 7 | a0001c0004t0001g0006 a0001c0004t0001g0074 a0001c0004t0001g0075 others(4): Show |
8 | HG00642.hp2 HG01070.hp1 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.4004+67A>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201715605 | |||||||
| chr2:201715647 | G | A | 250 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(247): Show |
266 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.4004+25C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 25/33 | chr2 | 201715647 | |||||||
| chr2:201716466 | C | T | 2 | a0001c0003t0002g0011 a0001c0003t0002g0191 |
3 | NA18970.hp1 NA19054.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.3837-627G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 24/33 | chr2 | 201716466 | |||||||
| chr2:201716492 | T | C | 327 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(324): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.3837-653A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 24/33 | chr2 | 201716492 | |||||||
| chr2:201716542 | C | CA | 121 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(118): Show |
133 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.3837-704dupT | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 24/33 | chr2 | 201716542 | |||||||
| chr2:201716542 | C | CAA | 63 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0266 others(60): Show |
70 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.3837-705_3837-704d others(4): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 24/33 | chr2 | 201716542 | |||||||
| chr2:201716542 | C | CAAA | 11 | a0001c0003t0001g0042 a0001c0003t0002g0162 a0001c0003t0002g0163 others(8): Show |
11 | HG00597.hp2 HG01175.hp2 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.3837-706_3837-704d others(5): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 24/33 | chr2 | 201716542 | |||||||
| chr2:201716542 | CA | C | 6 | a0001c0001t0003g0027 a0001c0002t0001g0054 a0001c0002t0001g0072 others(3): Show |
6 | HG01099.hp1 HG02451.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.3837-704delT | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 24/33 | chr2 | 201716542 | |||||||
| chr2:201716565 | A | G | 1 | a0001c0002t0001g0142 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.3837-726T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 24/33 | chr2 | 201716565 | |||||||
| chr2:201716665 | A | T | 2 | a0001c0002t0001g0221 a0001c0002t0001g0232 |
2 | HG01123.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.3837-826T>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 24/33 | chr2 | 201716665 | |||||||
| chr2:201716671 | C | T | 3 | a0001c0002t0001g0090 a0001c0002t0001g0091 a0001c0002t0001g0126 |
3 | HG01255.hp1 HG01517.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.3837-832G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 24/33 | chr2 | 201716671 | |||||||
| chr2:201716687 | C | T | 23 | a0001c0003t0007g0040 a0001c0003t0007g0041 a0001c0004t0001g0004 others(20): Show |
25 | HG00099.hp1 HG00642.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.3837-848G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 24/33 | chr2 | 201716687 | |||||||
| chr2:201716702 | G | A | 136 | a0001c0001t0001g0038 a0001c0001t0001g0081 a0001c0001t0001g0083 others(133): Show |
141 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.3837-863C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 24/33 | chr2 | 201716702 | |||||||
| chr2:201716706 | C | A | 11 | a0001c0004t0001g0004 a0001c0004t0001g0044 a0001c0004t0001g0045 others(8): Show |
12 | HG00099.hp1 HG00642.hp1 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.3837-867G>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 24/33 | chr2 | 201716706 | |||||||
| chr2:201716714 | CA | C | 16 | a0001c0002t0001g0069 a0001c0002t0001g0070 a0001c0002t0001g0071 others(13): Show |
16 | HG01952.hp1 NA18941.hp2 NA18942.hp2 others(13): Show |
intron_variant | MODIFIER | c.3837-876delT | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 24/33 | chr2 | 201716714 | |||||||
| chr2:201716737 | A | T | 1 | a0001c0003t0002g0168 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.3837-898T>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 24/33 | chr2 | 201716737 | |||||||
| chr2:201717004 | G | A | 7 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0210 others(4): Show |
7 | HG01243.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.3836+1073C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 24/33 | chr2 | 201717004 | |||||||
| chr2:201717045 | T | C | 191 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(188): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.3836+1032A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 24/33 | chr2 | 201717045 | |||||||
| chr2:201717184 | G | T | 1 | a0001c0001t0003g0028 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3836+893C>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 24/33 | chr2 | 201717184 | |||||||
| chr2:201717262 | C | G | 1 | a0001c0004t0003g0029 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3836+815G>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 24/33 | chr2 | 201717262 | |||||||
| chr2:201717262 | C | T | 1 | a0001c0011t0001g0321 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3836+815G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 24/33 | chr2 | 201717262 | |||||||
| chr2:201717391 | G | A | 55 | a0001c0003t0001g0042 a0001c0003t0002g0003 a0001c0003t0002g0009 others(52): Show |
60 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.3836+686C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 24/33 | chr2 | 201717391 | |||||||
| chr2:201717639 | GA | G | 65 | a0001c0001t0001g0260 a0001c0001t0001g0270 a0001c0001t0001g0288 others(62): Show |
70 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.3836+437delT | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 24/33 | chr2 | 201717639 | |||||||
| chr2:201717675 | G | A | 2 | a0001c0001t0006g0330 a0001c0001t0006g0331 |
2 | HG03098.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.3836+402C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 24/33 | chr2 | 201717675 | |||||||
| chr2:201718345 | C | T | 1 | a0001c0001t0001g0245 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3703-135G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201718345 | |||||||
| chr2:201718495 | A | G | 1 | a0001c0001t0001g0245 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3703-285T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201718495 | |||||||
| chr2:201718719 | C | A | 316 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(313): Show |
338 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(335): Show |
intron_variant | MODIFIER | c.3703-509G>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201718719 | |||||||
| chr2:201718806 | A | G | 1 | a0001c0002t0001g0108 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.3703-596T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201718806 | |||||||
| chr2:201718832 | G | A | 1 | a0001c0002t0001g0307 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.3703-622C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201718832 | |||||||
| chr2:201719316 | C | T | 2 | a0001c0001t0006g0330 a0001c0001t0006g0331 |
2 | HG03098.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.3703-1106G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201719316 | |||||||
| chr2:201719370 | C | T | 2 | a0001c0003t0007g0040 a0001c0003t0007g0041 |
2 | HG02622.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.3703-1160G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201719370 | |||||||
| chr2:201719391 | C | T | 1 | a0006c0012t0002g0161 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.3703-1181G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201719391 | |||||||
| chr2:201719481 | C | T | 1 | a0001c0004t0001g0157 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3703-1271G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201719481 | |||||||
| chr2:201719484 | G | A | 1 | a0001c0001t0001g0046 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3703-1274C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201719484 | |||||||
| chr2:201719514 | A | G | 1 | a0001c0003t0002g0299 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.3703-1304T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201719514 | |||||||
| chr2:201719590 | A | AAAAAAT | 51 | a0001c0002t0001g0121 a0001c0003t0002g0003 a0001c0003t0002g0009 others(48): Show |
56 | HG00544.hp1 HG00597.hp2 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.3703-1386_3703-138 others(10): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201719590 | |||||||
| chr2:201719590 | A | AAAAAATA others(5): Show |
1 | a0001c0003t0001g0042 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3703-1392_3703-138 others(16): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201719590 | |||||||
| chr2:201719590 | AAAAAAT | A | 21 | a0001c0004t0001g0004 a0001c0004t0001g0006 a0001c0004t0001g0044 others(18): Show |
23 | HG00099.hp1 HG00642.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.3703-1386_3703-138 others(10): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201719590 | |||||||
| chr2:201719590 | AAAAAATA others(5): Show |
A | 110 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(107): Show |
121 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.3703-1392_3703-138 others(16): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201719590 | |||||||
| chr2:201719861 | C | A | 21 | a0001c0004t0001g0004 a0001c0004t0001g0006 a0001c0004t0001g0044 others(18): Show |
23 | HG00099.hp1 HG00642.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.3703-1651G>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201719861 | |||||||
| chr2:201719943 | A | G | 7 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0210 others(4): Show |
7 | HG01243.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.3703-1733T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201719943 | |||||||
| chr2:201720196 | T | C | 1 | a0001c0001t0008g0279 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.3703-1986A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201720196 | |||||||
| chr2:201720224 | C | G | 23 | a0001c0003t0007g0040 a0001c0003t0007g0041 a0001c0004t0001g0004 others(20): Show |
25 | HG00099.hp1 HG00642.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.3703-2014G>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201720224 | |||||||
| chr2:201720267 | C | A | 1 | a0001c0004t0003g0029 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3703-2057G>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201720267 | |||||||
| chr2:201720417 | T | C | 4 | a0001c0004t0001g0004 a0001c0004t0001g0048 a0001c0004t0001g0049 others(1): Show |
5 | HG00642.hp1 HG00738.hp2 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.3703-2207A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201720417 | |||||||
| chr2:201720468 | C | T | 1 | a0001c0002t0001g0121 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.3703-2258G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201720468 | |||||||
| chr2:201720469 | G | A | 111 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(108): Show |
122 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.3703-2259C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201720469 | |||||||
| chr2:201720505 | C | T | 54 | a0001c0003t0002g0003 a0001c0003t0002g0009 a0001c0003t0002g0010 others(51): Show |
59 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.3703-2295G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201720505 | |||||||
| chr2:201720539 | C | CAA | 41 | a0001c0003t0002g0003 a0001c0003t0002g0009 a0001c0003t0002g0010 others(38): Show |
46 | HG00140.hp1 HG00621.hp1 HG01099.hp2 others(43): Show |
intron_variant | MODIFIER | c.3703-2331_3703-233 others(6): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201720539 | |||||||
| chr2:201720539 | C | CAAA | 13 | a0001c0003t0002g0088 a0001c0003t0002g0162 a0001c0003t0002g0171 others(10): Show |
13 | HG00544.hp1 HG00597.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.3703-2332_3703-233 others(7): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201720539 | |||||||
| chr2:201720539 | CA | C | 222 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(219): Show |
238 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.3703-2330delT | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201720539 | |||||||
| chr2:201720539 | CAA | C | 20 | a0001c0001t0003g0027 a0001c0002t0001g0128 a0001c0004t0001g0004 others(17): Show |
22 | HG00099.hp1 HG00642.hp1 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.3703-2331_3703-233 others(6): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201720539 | |||||||
| chr2:201720599 | A | T | 1 | a0001c0002t0001g0139 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.3703-2389T>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201720599 | |||||||
| chr2:201720608 | G | C | 1 | a0001c0001t0001g0325 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.3703-2398C>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201720608 | |||||||
| chr2:201720628 | C | G | 103 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(100): Show |
114 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.3702+2415G>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201720628 | |||||||
| chr2:201720714 | A | AAC | 7 | a0001c0001t0001g0083 a0001c0002t0001g0070 a0001c0003t0001g0042 others(4): Show |
7 | HG01081.hp1 HG02083.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.3702+2327_3702+232 others(6): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201720714 | |||||||
| chr2:201720714 | AACACAC | A | 111 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(108): Show |
122 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.3702+2323_3702+232 others(10): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201720714 | |||||||
| chr2:201720918 | T | C | 7 | a0001c0004t0001g0006 a0001c0004t0001g0074 a0001c0004t0001g0075 others(4): Show |
8 | HG00642.hp2 HG01070.hp1 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.3702+2125A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201720918 | |||||||
| chr2:201720963 | A | C | 23 | a0001c0003t0007g0040 a0001c0003t0007g0041 a0001c0004t0001g0004 others(20): Show |
25 | HG00099.hp1 HG00642.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.3702+2080T>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201720963 | |||||||
| chr2:201721155 | A | G | 327 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(324): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.3702+1888T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201721155 | |||||||
| chr2:201721390 | A | C | 1 | a0001c0004t0001g0079 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.3702+1653T>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201721390 | |||||||
| chr2:201721506 | T | G | 1 | a0001c0004t0001g0216 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.3702+1537A>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201721506 | |||||||
| chr2:201721572 | G | A | 1 | a0001c0002t0001g0123 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.3702+1471C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201721572 | |||||||
| chr2:201721587 | T | G | 1 | a0001c0002t0001g0135 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3702+1456A>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201721587 | |||||||
| chr2:201721620 | T | C | 1 | a0001c0003t0002g0170 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.3702+1423A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201721620 | |||||||
| chr2:201721672 | AT | A | 190 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(187): Show |
208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.3702+1370delA | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201721672 | |||||||
| chr2:201721764 | C | T | 7 | a0001c0001t0001g0017 a0001c0001t0001g0260 a0001c0001t0001g0291 others(4): Show |
8 | HG02258.hp1 HG02486.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.3702+1279G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201721764 | |||||||
| chr2:201721846 | G | A | 2 | a0001c0001t0001g0081 a0001c0001t0003g0031 |
2 | HG02055.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.3702+1197C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201721846 | |||||||
| chr2:201722230 | T | C | 1 | a0001c0003t0001g0042 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3702+813A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201722230 | |||||||
| chr2:201722236 | T | G | 1 | a0001c0003t0002g0190 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.3702+807A>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201722236 | |||||||
| chr2:201722347 | T | C | 111 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(108): Show |
122 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.3702+696A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201722347 | |||||||
| chr2:201722355 | A | T | 1 | a0001c0001t0001g0278 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.3702+688T>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201722355 | |||||||
| chr2:201722543 | T | C | 2 | a0001c0002t0001g0151 a0001c0002t0001g0152 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.3702+500A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201722543 | |||||||
| chr2:201722592 | T | C | 5 | a0001c0001t0001g0260 a0003c0007t0001g0034 a0003c0007t0001g0036 others(2): Show |
5 | HG02258.hp1 HG02486.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.3702+451A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201722592 | |||||||
| chr2:201722630 | C | T | 190 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(187): Show |
208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.3702+413G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201722630 | |||||||
| chr2:201722727 | T | G | 7 | a0001c0004t0001g0006 a0001c0004t0001g0074 a0001c0004t0001g0075 others(4): Show |
8 | HG00642.hp2 HG01070.hp1 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.3702+316A>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201722727 | |||||||
| chr2:201722860 | C | A | 23 | a0001c0003t0007g0040 a0001c0003t0007g0041 a0001c0004t0001g0004 others(20): Show |
25 | HG00099.hp1 HG00642.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.3702+183G>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201722860 | |||||||
| chr2:201722860 | C | T | 1 | a0009c0016t0001g0130 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.3702+183G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201722860 | |||||||
| chr2:201722863 | T | C | 23 | a0001c0003t0007g0040 a0001c0003t0007g0041 a0001c0004t0001g0004 others(20): Show |
25 | HG00099.hp1 HG00642.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.3702+180A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201722863 | |||||||
| chr2:201722930 | C | T | 190 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(187): Show |
208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.3702+113G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201722930 | |||||||
| chr2:201722936 | C | A | 7 | a0001c0004t0001g0006 a0001c0004t0001g0074 a0001c0004t0001g0075 others(4): Show |
8 | HG00642.hp2 HG01070.hp1 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.3702+107G>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201722936 | |||||||
| chr2:201722979 | A | G | 1 | a0001c0001t0001g0227 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.3702+64T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201722979 | |||||||
| chr2:201722983 | T | TA | 54 | a0001c0003t0002g0003 a0001c0003t0002g0009 a0001c0003t0002g0010 others(51): Show |
59 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.3702+59dupT | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201722983 | |||||||
| chr2:201723019 | A | G | 2 | a0001c0004t0001g0216 a0001c0004t0003g0029 |
2 | HG02027.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.3702+24T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 23/33 | chr2 | 201723019 | |||||||
| chr2:201723527 | C | T | 9 | a0001c0004t0001g0004 a0001c0004t0001g0044 a0001c0004t0001g0045 others(6): Show |
10 | HG00099.hp1 HG00642.hp1 HG00738.hp2 others(7): Show |
intron_variant | MODIFIER | c.3513-86G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 21/33 | chr2 | 201723527 | |||||||
| chr2:201723607 | T | C | 21 | a0001c0004t0001g0004 a0001c0004t0001g0006 a0001c0004t0001g0044 others(18): Show |
23 | HG00099.hp1 HG00642.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.3513-166A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 21/33 | chr2 | 201723607 | |||||||
| chr2:201723809 | A | G | 1 | a0001c0003t0002g0194 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3513-368T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 21/33 | chr2 | 201723809 | |||||||
| chr2:201723857 | C | T | 2 | a0001c0001t0006g0330 a0001c0001t0006g0331 |
2 | HG03098.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.3513-416G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 21/33 | chr2 | 201723857 | |||||||
| chr2:201723979 | G | A | 21 | a0001c0004t0001g0004 a0001c0004t0001g0006 a0001c0004t0001g0044 others(18): Show |
23 | HG00099.hp1 HG00642.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.3512+316C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 21/33 | chr2 | 201723979 | |||||||
| chr2:201724062 | G | C | 2 | a0001c0004t0001g0216 a0001c0004t0003g0029 |
2 | HG02027.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.3512+233C>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 21/33 | chr2 | 201724062 | |||||||
| chr2:201724534 | T | C | 113 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(110): Show |
124 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.3348-75A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 20/33 | chr2 | 201724534 | |||||||
| chr2:201724772 | T | C | 21 | a0001c0004t0001g0004 a0001c0004t0001g0006 a0001c0004t0001g0044 others(18): Show |
23 | HG00099.hp1 HG00642.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.3348-313A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 20/33 | chr2 | 201724772 | |||||||
| chr2:201724794 | T | C | 21 | a0001c0004t0001g0004 a0001c0004t0001g0006 a0001c0004t0001g0044 others(18): Show |
23 | HG00099.hp1 HG00642.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.3348-335A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 20/33 | chr2 | 201724794 | |||||||
| chr2:201724835 | T | C | 191 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(188): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.3348-376A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 20/33 | chr2 | 201724835 | |||||||
| chr2:201724841 | C | T | 1 | a0001c0001t0003g0026 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3348-382G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 20/33 | chr2 | 201724841 | |||||||
| chr2:201724909 | C | G | 2 | a0001c0004t0001g0216 a0001c0004t0003g0029 |
2 | HG02027.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.3347+447G>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 20/33 | chr2 | 201724909 | |||||||
| chr2:201724968 | C | A | 1 | a0002c0005t0001g0066 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.3347+388G>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 20/33 | chr2 | 201724968 | |||||||
| chr2:201724972 | G | A | 1 | a0001c0001t0001g0319 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.3347+384C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 20/33 | chr2 | 201724972 | |||||||
| chr2:201725069 | C | T | 21 | a0001c0004t0001g0004 a0001c0004t0001g0006 a0001c0004t0001g0044 others(18): Show |
23 | HG00099.hp1 HG00642.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.3347+287G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 20/33 | chr2 | 201725069 | |||||||
| chr2:201725094 | C | A | 1 | a0001c0022t0001g0124 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.3347+262G>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 20/33 | chr2 | 201725094 | |||||||
| chr2:201725108 | A | G | 21 | a0001c0004t0001g0004 a0001c0004t0001g0006 a0001c0004t0001g0044 others(18): Show |
23 | HG00099.hp1 HG00642.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.3347+248T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 20/33 | chr2 | 201725108 | |||||||
| chr2:201725112 | C | CA | 15 | a0001c0002t0001g0090 a0001c0002t0001g0114 a0001c0002t0001g0134 others(12): Show |
17 | HG00099.hp1 HG00642.hp1 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.3347+243dupT | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 20/33 | chr2 | 201725112 | |||||||
| chr2:201725697 | CAGA | C | 9 | a0001c0001t0001g0237 a0001c0001t0001g0241 a0001c0001t0001g0250 others(6): Show |
9 | HG00597.hp1 HG00673.hp1 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.3249-246_3249-244d others(5): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 19/33 | chr2 | 201725697 | |||||||
| chr2:201725747 | C | G | 2 | a0001c0001t0006g0330 a0001c0001t0006g0331 |
2 | HG03098.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.3249-293G>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 19/33 | chr2 | 201725747 | |||||||
| chr2:201725847 | T | A | 7 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0210 others(4): Show |
7 | HG01243.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.3249-393A>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 19/33 | chr2 | 201725847 | |||||||
| chr2:201725991 | T | C | 1 | a0001c0001t0001g0288 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3248+493A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 19/33 | chr2 | 201725991 | |||||||
| chr2:201726162 | A | G | 21 | a0001c0004t0001g0004 a0001c0004t0001g0006 a0001c0004t0001g0044 others(18): Show |
23 | HG00099.hp1 HG00642.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.3248+322T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 19/33 | chr2 | 201726162 | |||||||
| chr2:201726163 | T | C | 1 | a0001c0001t0001g0046 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3248+321A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 19/33 | chr2 | 201726163 | |||||||
| chr2:201726277 | C | T | 2 | a0001c0001t0001g0248 a0001c0001t0001g0289 |
2 | HG04184.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.3248+207G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 19/33 | chr2 | 201726277 | |||||||
| chr2:201726434 | C | G | 1 | a0001c0003t0002g0184 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3248+50G>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 19/33 | chr2 | 201726434 | |||||||
| chr2:201726434 | C | T | 2 | a0001c0003t0002g0174 a0001c0003t0002g0199 |
2 | HG01168.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.3248+50G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 19/33 | chr2 | 201726434 | |||||||
| chr2:201726892 | A | T | 3 | a0001c0004t0001g0157 a0001c0004t0001g0216 a0001c0004t0003g0029 |
3 | HG01884.hp1 HG02027.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.2980-26T>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 17/33 | chr2 | 201726892 | |||||||
| chr2:201726991 | G | A | 1 | a0001c0003t0002g0176 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2980-125C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 17/33 | chr2 | 201726991 | |||||||
| chr2:201727046 | T | TA | 157 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(154): Show |
173 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.2979+165dupT | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 17/33 | chr2 | 201727046 | |||||||
| chr2:201727058 | C | A | 1 | a0001c0003t0002g0184 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2979+154G>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 17/33 | chr2 | 201727058 | |||||||
| chr2:201727087 | G | T | 2 | a0001c0001t0001g0242 a0001c0001t0001g0243 |
2 | HG02723.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2979+125C>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 17/33 | chr2 | 201727087 | |||||||
| chr2:201727098 | A | G | 2 | a0001c0004t0001g0216 a0001c0004t0003g0029 |
2 | HG02027.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.2979+114T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 17/33 | chr2 | 201727098 | |||||||
| chr2:201727131 | C | T | 1 | a0001c0002t0001g0140 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2979+81G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 17/33 | chr2 | 201727131 | |||||||
| chr2:201727303 | CCAGGA | C | 3 | a0001c0004t0001g0157 a0001c0004t0001g0216 a0001c0004t0003g0029 |
3 | HG01884.hp1 HG02027.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.2913-30_2913-26del others(5): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 16/33 | chr2 | 201727303 | |||||||
| chr2:201727336 | G | A | 13 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0022 others(10): Show |
15 | HG01109.hp2 HG01123.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.2913-58C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 16/33 | chr2 | 201727336 | |||||||
| chr2:201727480 | T | C | 6 | a0001c0001t0001g0260 a0003c0007t0001g0034 a0003c0007t0001g0036 others(3): Show |
6 | HG02258.hp1 HG02280.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.2913-202A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 16/33 | chr2 | 201727480 | |||||||
| chr2:201727791 | C | T | 9 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0206 others(6): Show |
11 | HG02451.hp2 HG02976.hp1 HG03041.hp1 others(8): Show |
intron_variant | MODIFIER | c.2842-16G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 15/33 | chr2 | 201727791 | |||||||
| chr2:201727795 | G | A | 1 | a0001c0002t0001g0107 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2842-20C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 15/33 | chr2 | 201727795 | |||||||
| chr2:201728251 | C | T | 53 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0017 others(50): Show |
60 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.2841+261G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 15/33 | chr2 | 201728251 | |||||||
| chr2:201728259 | C | T | 4 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0287 others(1): Show |
6 | HG02976.hp1 HG03139.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.2841+253G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 15/33 | chr2 | 201728259 | |||||||
| chr2:201728309 | T | C | 1 | a0002c0020t0001g0063 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2841+203A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 15/33 | chr2 | 201728309 | |||||||
| chr2:201728376 | G | A | 7 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0210 others(4): Show |
7 | HG01243.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.2841+136C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 15/33 | chr2 | 201728376 | |||||||
| chr2:201728463 | TA | T | 6 | a0001c0001t0001g0222 a0001c0001t0001g0227 a0001c0001t0001g0280 others(3): Show |
7 | HG01515.hp2 HG01517.hp2 HG02004.hp2 others(4): Show |
intron_variant | MODIFIER | c.2841+48delT | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 15/33 | chr2 | 201728463 | |||||||
| chr2:201728736 | A | G | 22 | a0001c0001t0001g0217 a0001c0004t0001g0004 a0001c0004t0001g0006 others(19): Show |
24 | HG00099.hp1 HG00642.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.2713-96T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 14/33 | chr2 | 201728736 | |||||||
| chr2:201728746 | C | T | 1 | a0001c0003t0002g0169 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.2713-106G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 14/33 | chr2 | 201728746 | |||||||
| chr2:201728827 | GA | G | 14 | a0001c0002t0001g0092 a0001c0002t0001g0093 a0001c0002t0001g0096 others(11): Show |
14 | HG04184.hp2 NA18951.hp1 NA18959.hp2 others(11): Show |
intron_variant | MODIFIER | c.2713-188delT | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 14/33 | chr2 | 201728827 | |||||||
| chr2:201728834 | AAAAC | A | 57 | a0001c0003t0001g0172 a0001c0003t0002g0003 a0001c0003t0002g0009 others(54): Show |
62 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.2713-198_2713-195d others(6): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 14/33 | chr2 | 201728834 | |||||||
| chr2:201728950 | G | C | 1 | a0001c0001t0001g0253 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2712+102C>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 14/33 | chr2 | 201728950 | |||||||
| chr2:201729316 | A | G | 117 | a0001c0001t0001g0081 a0001c0001t0003g0020 a0001c0001t0003g0021 others(114): Show |
121 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.2581-133T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201729316 | |||||||
| chr2:201729434 | G | A | 1 | a0002c0006t0005g0060 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2581-251C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201729434 | |||||||
| chr2:201729457 | A | G | 22 | a0001c0001t0001g0217 a0001c0004t0001g0004 a0001c0004t0001g0006 others(19): Show |
24 | HG00099.hp1 HG00642.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.2581-274T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201729457 | |||||||
| chr2:201729474 | A | G | 22 | a0001c0001t0001g0217 a0001c0004t0001g0004 a0001c0004t0001g0006 others(19): Show |
24 | HG00099.hp1 HG00642.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.2581-291T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201729474 | |||||||
| chr2:201729484 | C | T | 1 | a0001c0022t0001g0124 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2581-301G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201729484 | |||||||
| chr2:201729609 | G | A | 2 | a0001c0001t0001g0259 a0001c0001t0003g0023 |
2 | HG02559.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2581-426C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201729609 | |||||||
| chr2:201729638 | T | C | 1 | a0001c0003t0001g0042 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2581-455A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201729638 | |||||||
| chr2:201729646 | C | T | 2 | a0001c0003t0007g0040 a0001c0003t0007g0041 |
2 | HG02622.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2581-463G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201729646 | |||||||
| chr2:201729737 | C | T | 114 | a0001c0001t0003g0020 a0001c0001t0003g0022 a0001c0001t0003g0023 others(111): Show |
118 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.2581-554G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201729737 | |||||||
| chr2:201729753 | C | T | 2 | a0001c0001t0001g0283 a0001c0001t0001g0284 |
2 | NA18942.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.2581-570G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201729753 | |||||||
| chr2:201729879 | CA | C | 206 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(203): Show |
220 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.2581-697delT | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201729879 | |||||||
| chr2:201729879 | CAA | C | 70 | a0001c0001t0001g0217 a0001c0001t0001g0284 a0001c0002t0001g0086 others(67): Show |
77 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.2581-698_2581-697d others(4): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201729879 | |||||||
| chr2:201729897 | A | C | 23 | a0001c0001t0001g0038 a0001c0001t0001g0083 a0001c0001t0001g0205 others(20): Show |
24 | HG01074.hp1 HG01243.hp2 HG01255.hp2 others(21): Show |
intron_variant | MODIFIER | c.2581-714T>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201729897 | |||||||
| chr2:201729898 | A | G | 1 | a0001c0001t0001g0318 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2581-715T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201729898 | |||||||
| chr2:201729901 | A | C | 2 | a0001c0001t0006g0330 a0001c0001t0006g0331 |
2 | HG03098.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2581-718T>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201729901 | |||||||
| chr2:201729993 | A | G | 1 | a0001c0002t0001g0233 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2581-810T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201729993 | |||||||
| chr2:201730070 | A | G | 3 | a0001c0002t0001g0131 a0001c0002t0001g0133 a0001c0002t0001g0158 |
3 | HG00738.hp1 HG01433.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2581-887T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201730070 | |||||||
| chr2:201730185 | A | G | 103 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(100): Show |
114 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.2581-1002T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201730185 | |||||||
| chr2:201730225 | G | A | 1 | a0002c0005t0001g0056 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2581-1042C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201730225 | |||||||
| chr2:201730325 | T | C | 22 | a0001c0001t0001g0217 a0001c0004t0001g0004 a0001c0004t0001g0006 others(19): Show |
24 | HG00099.hp1 HG00642.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.2581-1142A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201730325 | |||||||
| chr2:201730579 | G | A | 1 | a0001c0003t0007g0041 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2581-1396C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201730579 | |||||||
| chr2:201730633 | A | T | 116 | a0001c0001t0001g0234 a0001c0001t0003g0020 a0001c0001t0003g0021 others(113): Show |
120 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.2581-1450T>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201730633 | |||||||
| chr2:201730671 | TCTCAA | T | 22 | a0001c0001t0001g0217 a0001c0004t0001g0004 a0001c0004t0001g0006 others(19): Show |
24 | HG00099.hp1 HG00642.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.2581-1493_2581-148 others(9): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201730671 | |||||||
| chr2:201730681 | A | C | 1 | a0001c0001t0001g0280 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2581-1498T>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201730681 | |||||||
| chr2:201730693 | A | G | 22 | a0001c0001t0001g0217 a0001c0004t0001g0004 a0001c0004t0001g0006 others(19): Show |
24 | HG00099.hp1 HG00642.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.2581-1510T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201730693 | |||||||
| chr2:201730840 | T | A | 1 | a0001c0003t0001g0042 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2581-1657A>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201730840 | |||||||
| chr2:201730843 | T | C | 2 | a0001c0011t0001g0084 a0001c0011t0001g0321 |
2 | HG02615.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2581-1660A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201730843 | |||||||
| chr2:201730871 | T | C | 1 | a0006c0012t0002g0161 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.2581-1688A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201730871 | |||||||
| chr2:201730994 | G | T | 1 | a0010c0014t0001g0043 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2581-1811C>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201730994 | |||||||
| chr2:201731063 | A | C | 1 | a0001c0003t0002g0185 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.2581-1880T>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201731063 | |||||||
| chr2:201731135 | T | C | 1 | a0001c0004t0001g0157 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2581-1952A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201731135 | |||||||
| chr2:201731144 | T | C | 210 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(207): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.2581-1961A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201731144 | |||||||
| chr2:201731242 | G | GA | 22 | a0001c0001t0001g0217 a0001c0004t0001g0004 a0001c0004t0001g0006 others(19): Show |
24 | HG00099.hp1 HG00642.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.2580+2033dupT | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201731242 | |||||||
| chr2:201731399 | A | G | 2 | a0001c0001t0006g0330 a0001c0001t0006g0331 |
2 | HG03098.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2580+1877T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201731399 | |||||||
| chr2:201731412 | CA | C | 3 | a0001c0001t0001g0318 a0001c0001t0001g0319 a0001c0001t0001g0322 |
3 | NA18966.hp1 NA18973.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.2580+1863delT | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201731412 | |||||||
| chr2:201731574 | T | C | 1 | a0010c0014t0001g0043 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2580+1702A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201731574 | |||||||
| chr2:201731677 | A | G | 9 | a0001c0001t0001g0256 a0001c0001t0001g0269 a0001c0001t0001g0270 others(6): Show |
9 | HG00558.hp1 HG02015.hp1 NA18956.hp1 others(6): Show |
intron_variant | MODIFIER | c.2580+1599T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201731677 | |||||||
| chr2:201731683 | AC | A | 22 | a0001c0001t0001g0217 a0001c0004t0001g0004 a0001c0004t0001g0006 others(19): Show |
24 | HG00099.hp1 HG00642.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.2580+1592delG | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201731683 | |||||||
| chr2:201731794 | T | C | 1 | a0001c0002t0001g0140 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2580+1482A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201731794 | |||||||
| chr2:201731806 | G | T | 58 | a0001c0003t0001g0042 a0001c0003t0001g0172 a0001c0003t0002g0003 others(55): Show |
63 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.2580+1470C>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201731806 | |||||||
| chr2:201731862 | C | G | 127 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(124): Show |
139 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.2580+1414G>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201731862 | |||||||
| chr2:201731867 | T | C | 9 | a0001c0004t0001g0004 a0001c0004t0001g0044 a0001c0004t0001g0045 others(6): Show |
10 | HG00099.hp1 HG00642.hp1 HG00738.hp2 others(7): Show |
intron_variant | MODIFIER | c.2580+1409A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201731867 | |||||||
| chr2:201731894 | T | C | 1 | a0001c0001t0001g0261 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2580+1382A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201731894 | |||||||
| chr2:201731930 | G | A | 1 | a0001c0002t0001g0126 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2580+1346C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201731930 | |||||||
| chr2:201731986 | A | G | 1 | a0001c0004t0001g0050 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2580+1290T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201731986 | |||||||
| chr2:201732033 | A | G | 9 | a0001c0004t0001g0004 a0001c0004t0001g0044 a0001c0004t0001g0045 others(6): Show |
10 | HG00099.hp1 HG00642.hp1 HG00738.hp2 others(7): Show |
intron_variant | MODIFIER | c.2580+1243T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201732033 | |||||||
| chr2:201732070 | A | G | 1 | a0001c0001t0001g0255 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2580+1206T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201732070 | |||||||
| chr2:201732184 | T | A | 1 | a0001c0002t0001g0139 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2580+1092A>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201732184 | |||||||
| chr2:201732288 | T | C | 3 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0212 |
3 | HG02922.hp2 HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2580+988A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201732288 | |||||||
| chr2:201732399 | C | CA | 37 | a0001c0001t0001g0038 a0001c0001t0001g0083 a0001c0001t0001g0205 others(34): Show |
39 | HG00738.hp1 HG01074.hp1 HG01243.hp2 others(36): Show |
intron_variant | MODIFIER | c.2580+876dupT | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201732399 | |||||||
| chr2:201732399 | C | CAA | 7 | a0001c0001t0001g0212 a0001c0001t0001g0260 a0003c0007t0001g0034 others(4): Show |
7 | HG02258.hp1 HG02280.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.2580+875_2580+876d others(4): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201732399 | |||||||
| chr2:201732399 | CA | C | 78 | a0001c0001t0001g0046 a0001c0001t0001g0217 a0001c0001t0001g0277 others(75): Show |
85 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.2580+876delT | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201732399 | |||||||
| chr2:201732712 | T | C | 22 | a0001c0001t0001g0217 a0001c0004t0001g0004 a0001c0004t0001g0006 others(19): Show |
24 | HG00099.hp1 HG00642.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.2580+564A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201732712 | |||||||
| chr2:201732906 | G | T | 116 | a0001c0001t0001g0081 a0001c0001t0003g0020 a0001c0001t0003g0022 others(113): Show |
120 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.2580+370C>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201732906 | |||||||
| chr2:201732914 | C | A | 116 | a0001c0001t0001g0081 a0001c0001t0003g0020 a0001c0001t0003g0022 others(113): Show |
120 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.2580+362G>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201732914 | |||||||
| chr2:201732956 | C | T | 1 | a0001c0001t0001g0257 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2580+320G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201732956 | |||||||
| chr2:201733026 | A | T | 3 | a0001c0001t0001g0217 a0001c0004t0001g0216 a0001c0004t0003g0029 |
3 | HG02027.hp2 HG02145.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.2580+250T>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 13/33 | chr2 | 201733026 | |||||||
| chr2:201733492 | T | C | 1 | a0001c0003t0002g0198 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.2418-54A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201733492 | |||||||
| chr2:201733804 | T | C | 2 | a0001c0001t0006g0330 a0001c0001t0006g0331 |
2 | HG03098.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2418-366A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201733804 | |||||||
| chr2:201733897 | C | A | 1 | a0001c0002t0001g0114 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.2418-459G>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201733897 | |||||||
| chr2:201734170 | T | A | 8 | a0001c0001t0001g0246 a0001c0001t0001g0275 a0001c0001t0001g0276 others(5): Show |
8 | HG02165.hp2 NA18940.hp2 NA18986.hp2 others(5): Show |
intron_variant | MODIFIER | c.2418-732A>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201734170 | |||||||
| chr2:201734265 | G | A | 58 | a0001c0003t0001g0042 a0001c0003t0001g0172 a0001c0003t0002g0003 others(55): Show |
63 | HG00140.hp1 HG00544.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.2418-827C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201734265 | |||||||
| chr2:201734291 | A | G | 1 | a0001c0002t0001g0153 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.2418-853T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201734291 | |||||||
| chr2:201734420 | A | T | 12 | a0001c0002t0001g0092 a0001c0002t0001g0093 a0001c0002t0001g0096 others(9): Show |
12 | HG04184.hp2 NA18951.hp1 NA18959.hp2 others(9): Show |
intron_variant | MODIFIER | c.2418-982T>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201734420 | |||||||
| chr2:201734428 | T | C | 103 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(100): Show |
114 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.2418-990A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201734428 | |||||||
| chr2:201734450 | G | A | 1 | a0001c0004t0001g0048 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.2418-1012C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201734450 | |||||||
| chr2:201734467 | C | CAAAAAAA others(6): Show |
2 | a0001c0004t0001g0047 a0010c0014t0001g0043 |
2 | HG01884.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.2418-1042_2418-103 others(17): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201734467 | |||||||
| chr2:201734467 | C | CAAAAAAA others(7): Show |
14 | a0001c0001t0001g0217 a0001c0004t0001g0006 a0001c0004t0001g0044 others(11): Show |
15 | HG00099.hp1 HG00642.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.2418-1030_2418-102 others(18): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201734467 | |||||||
| chr2:201734467 | C | CAAAAAAA others(8): Show |
4 | a0001c0004t0001g0004 a0001c0004t0001g0048 a0001c0004t0001g0157 others(1): Show |
5 | HG00642.hp1 HG00738.hp2 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.2418-1030_2418-102 others(19): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201734467 | |||||||
| chr2:201734467 | C | CAAAAAAA others(9): Show |
2 | a0001c0004t0001g0049 a0001c0004t0001g0050 |
2 | HG01361.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.2418-1030_2418-102 others(20): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201734467 | |||||||
| chr2:201734527 | A | C | 1 | a0001c0001t0001g0287 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2418-1089T>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201734527 | |||||||
| chr2:201734550 | G | A | 3 | a0001c0001t0001g0264 a0001c0001t0001g0268 a0001c0001t0001g0272 |
3 | HG00621.hp2 NA19056.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.2418-1112C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201734550 | |||||||
| chr2:201734775 | G | A | 5 | a0003c0007t0001g0034 a0003c0007t0001g0036 a0003c0007t0001g0037 others(2): Show |
5 | HG02258.hp1 HG02280.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.2418-1337C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201734775 | |||||||
| chr2:201734924 | T | TA | 12 | a0001c0001t0001g0046 a0001c0004t0001g0004 a0001c0004t0001g0044 others(9): Show |
13 | HG00099.hp1 HG00642.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.2418-1487dupT | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201734924 | |||||||
| chr2:201735048 | G | A | 23 | a0001c0001t0001g0046 a0001c0001t0001g0217 a0001c0004t0001g0004 others(20): Show |
25 | HG00099.hp1 HG00642.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.2418-1610C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201735048 | |||||||
| chr2:201735154 | C | T | 138 | a0001c0001t0001g0046 a0001c0001t0001g0083 a0001c0001t0001g0149 others(135): Show |
144 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.2418-1716G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201735154 | |||||||
| chr2:201735172 | G | A | 1 | a0010c0014t0001g0043 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2418-1734C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201735172 | |||||||
| chr2:201735199 | C | A | 1 | a0001c0001t0001g0296 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2418-1761G>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201735199 | |||||||
| chr2:201735211 | G | A | 2 | a0001c0003t0007g0040 a0001c0003t0007g0041 |
2 | HG02622.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2418-1773C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201735211 | |||||||
| chr2:201735341 | T | G | 1 | a0001c0004t0001g0157 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2418-1903A>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201735341 | |||||||
| chr2:201735394 | G | A | 145 | a0001c0001t0001g0038 a0001c0001t0001g0046 a0001c0001t0001g0081 others(142): Show |
151 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.2418-1956C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201735394 | |||||||
| chr2:201735835 | C | G | 1 | a0001c0004t0001g0079 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2418-2397G>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201735835 | |||||||
| chr2:201735851 | T | C | 10 | a0001c0001t0003g0020 a0001c0001t0003g0022 a0001c0001t0003g0023 others(7): Show |
10 | HG01109.hp2 HG01123.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.2418-2413A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201735851 | |||||||
| chr2:201735978 | C | G | 1 | a0001c0001t0003g0020 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2418-2540G>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201735978 | |||||||
| chr2:201736044 | A | G | 7 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0210 others(4): Show |
7 | HG01243.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.2418-2606T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201736044 | |||||||
| chr2:201736066 | T | C | 1 | a0010c0014t0001g0043 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2417+2604A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201736066 | |||||||
| chr2:201736286 | A | G | 2 | a0001c0001t0001g0038 a0001c0003t0001g0042 |
2 | HG02486.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2417+2384T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201736286 | |||||||
| chr2:201736431 | G | A | 1 | a0001c0003t0002g0190 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2417+2239C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201736431 | |||||||
| chr2:201736467 | T | C | 2 | a0001c0003t0002g0174 a0001c0003t0002g0199 |
2 | HG01168.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.2417+2203A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201736467 | |||||||
| chr2:201736550 | G | A | 1 | a0001c0003t0004g0166 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2417+2120C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201736550 | |||||||
| chr2:201736629 | G | A | 3 | a0001c0003t0004g0154 a0001c0003t0004g0155 a0001c0003t0004g0156 |
3 | HG00741.hp1 HG01099.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.2417+2041C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201736629 | |||||||
| chr2:201736684 | C | T | 129 | a0001c0001t0001g0046 a0001c0001t0001g0081 a0001c0001t0001g0083 others(126): Show |
133 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.2417+1986G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201736684 | |||||||
| chr2:201736783 | T | C | 127 | a0001c0001t0001g0046 a0001c0001t0001g0081 a0001c0001t0001g0083 others(124): Show |
131 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.2417+1887A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201736783 | |||||||
| chr2:201737014 | T | C | 127 | a0001c0001t0001g0046 a0001c0001t0001g0081 a0001c0001t0001g0083 others(124): Show |
131 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.2417+1656A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201737014 | |||||||
| chr2:201737060 | A | G | 4 | a0002c0005t0001g0056 a0002c0005t0001g0065 a0002c0005t0001g0066 others(1): Show |
4 | HG01074.hp1 HG01255.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.2417+1610T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201737060 | |||||||
| chr2:201737171 | T | A | 129 | a0001c0001t0001g0046 a0001c0001t0001g0081 a0001c0001t0001g0083 others(126): Show |
133 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.2417+1499A>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201737171 | |||||||
| chr2:201737187 | G | C | 1 | a0004c0008t0001g0236 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2417+1483C>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201737187 | |||||||
| chr2:201737662 | C | T | 108 | a0001c0001t0001g0081 a0001c0001t0001g0083 a0001c0001t0001g0149 others(105): Show |
110 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.2417+1008G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201737662 | |||||||
| chr2:201737672 | G | A | 1 | a0001c0003t0002g0162 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2417+998C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201737672 | |||||||
| chr2:201737900 | T | C | 126 | a0001c0001t0001g0046 a0001c0001t0001g0081 a0001c0001t0001g0083 others(123): Show |
130 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.2417+770A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201737900 | |||||||
| chr2:201737909 | G | A | 1 | a0001c0002t0001g0127 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2417+761C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201737909 | |||||||
| chr2:201737916 | C | T | 2 | a0001c0001t0003g0027 a0001c0001t0003g0028 |
2 | HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2417+754G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201737916 | |||||||
| chr2:201737921 | C | CA | 8 | a0001c0001t0001g0038 a0001c0004t0001g0006 a0001c0004t0001g0074 others(5): Show |
9 | HG00642.hp2 HG01070.hp1 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.2417+748dupT | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201737921 | |||||||
| chr2:201737926 | A | C | 1 | a0001c0011t0001g0321 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2417+744T>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201737926 | |||||||
| chr2:201737956 | A | C | 2 | a0001c0001t0001g0217 a0001c0004t0001g0216 |
2 | HG02027.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.2417+714T>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201737956 | |||||||
| chr2:201737970 | G | C | 1 | a0001c0004t0001g0074 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2417+700C>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201737970 | |||||||
| chr2:201738066 | T | C | 317 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(314): Show |
337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.2417+604A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201738066 | |||||||
| chr2:201738091 | G | C | 127 | a0001c0001t0001g0046 a0001c0001t0001g0081 a0001c0001t0001g0083 others(124): Show |
131 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.2417+579C>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201738091 | |||||||
| chr2:201738163 | C | T | 327 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(324): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.2417+507G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201738163 | |||||||
| chr2:201738164 | A | G | 1 | a0010c0014t0001g0043 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2417+506T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201738164 | |||||||
| chr2:201738269 | G | C | 1 | a0001c0001t0001g0303 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2417+401C>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201738269 | |||||||
| chr2:201738424 | A | G | 120 | a0001c0001t0001g0046 a0001c0001t0001g0081 a0001c0001t0001g0083 others(117): Show |
123 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.2417+246T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201738424 | |||||||
| chr2:201738489 | T | C | 1 | a0001c0001t0001g0312 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2417+181A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 12/33 | chr2 | 201738489 | |||||||
| chr2:201738817 | T | C | 1 | a0001c0001t0008g0279 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2352-82A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 11/33 | chr2 | 201738817 | |||||||
| chr2:201738867 | A | T | 1 | a0001c0003t0002g0185 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.2352-132T>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 11/33 | chr2 | 201738867 | |||||||
| chr2:201739071 | T | C | 119 | a0001c0001t0001g0046 a0001c0001t0001g0081 a0001c0001t0001g0083 others(116): Show |
122 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.2352-336A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 11/33 | chr2 | 201739071 | |||||||
| chr2:201739114 | C | T | 119 | a0001c0001t0001g0046 a0001c0001t0001g0081 a0001c0001t0001g0083 others(116): Show |
122 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.2352-379G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 11/33 | chr2 | 201739114 | |||||||
| chr2:201739128 | ACTTGGGA others(1081): Show |
A | 2 | a0001c0001t0001g0038 a0001c0003t0001g0042 |
2 | HG02486.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2351+1458_2352-394 others(3): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 11/33 | chr2 | 201739128 | |||||||
| chr2:201739189 | T | C | 1 | a0001c0011t0001g0321 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2352-454A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 11/33 | chr2 | 201739189 | |||||||
| chr2:201739232 | T | TC | 105 | a0001c0001t0001g0083 a0001c0001t0001g0149 a0001c0001t0001g0217 others(102): Show |
108 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.2352-498dupG | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 11/33 | chr2 | 201739232 | |||||||
| chr2:201739235 | C | CCA | 10 | a0001c0001t0001g0046 a0001c0001t0001g0081 a0001c0002t0001g0114 others(7): Show |
10 | HG00099.hp1 HG01081.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.2352-501_2352-500i others(4): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 11/33 | chr2 | 201739235 | |||||||
| chr2:201739235 | CA | C | 144 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(141): Show |
159 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.2352-501delT | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 11/33 | chr2 | 201739235 | |||||||
| chr2:201739235 | CAA | C | 11 | a0001c0001t0001g0206 a0001c0001t0001g0278 a0001c0001t0001g0286 others(8): Show |
11 | HG01496.hp2 HG01943.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.2352-502_2352-501d others(4): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 11/33 | chr2 | 201739235 | |||||||
| chr2:201739236 | A | C | 5 | a0001c0002t0001g0086 a0001c0002t0001g0101 a0001c0002t0001g0141 others(2): Show |
5 | HG03195.hp1 HG03209.hp2 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.2352-501T>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 11/33 | chr2 | 201739236 | |||||||
| chr2:201739237 | A | C | 4 | a0003c0007t0001g0034 a0003c0007t0001g0037 a0003c0007t0001g0080 others(1): Show |
4 | HG02258.hp1 HG02280.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2352-502T>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 11/33 | chr2 | 201739237 | |||||||
| chr2:201739357 | C | T | 99 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(96): Show |
110 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.2352-622G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 11/33 | chr2 | 201739357 | |||||||
| chr2:201739410 | A | T | 1 | a0001c0001t0003g0024 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2352-675T>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 11/33 | chr2 | 201739410 | |||||||
| chr2:201739465 | G | A | 119 | a0001c0001t0001g0046 a0001c0001t0001g0081 a0001c0001t0001g0083 others(116): Show |
122 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.2352-730C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 11/33 | chr2 | 201739465 | |||||||
| chr2:201739508 | T | C | 306 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(303): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.2352-773A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 11/33 | chr2 | 201739508 | |||||||
| chr2:201739549 | C | G | 1 | a0001c0002t0001g0090 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2352-814G>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 11/33 | chr2 | 201739549 | |||||||
| chr2:201739763 | AAG | A | 12 | a0001c0001t0001g0046 a0001c0004t0001g0004 a0001c0004t0001g0044 others(9): Show |
13 | HG00099.hp1 HG00642.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.2352-1030_2352-102 others(6): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 11/33 | chr2 | 201739763 | |||||||
| chr2:201739952 | G | C | 119 | a0001c0001t0001g0046 a0001c0001t0001g0081 a0001c0001t0001g0083 others(116): Show |
122 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.2352-1217C>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 11/33 | chr2 | 201739952 | |||||||
| chr2:201740031 | A | G | 119 | a0001c0001t0001g0046 a0001c0001t0001g0081 a0001c0001t0001g0083 others(116): Show |
122 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.2352-1296T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 11/33 | chr2 | 201740031 | |||||||
| chr2:201740043 | C | G | 119 | a0001c0001t0001g0046 a0001c0001t0001g0081 a0001c0001t0001g0083 others(116): Show |
122 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.2352-1308G>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 11/33 | chr2 | 201740043 | |||||||
| chr2:201740171 | A | T | 119 | a0001c0001t0001g0046 a0001c0001t0001g0081 a0001c0001t0001g0083 others(116): Show |
122 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.2352-1436T>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 11/33 | chr2 | 201740171 | |||||||
| chr2:201740324 | A | C | 119 | a0001c0001t0001g0046 a0001c0001t0001g0081 a0001c0001t0001g0083 others(116): Show |
122 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.2351+1350T>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 11/33 | chr2 | 201740324 | |||||||
| chr2:201740385 | C | A | 119 | a0001c0001t0001g0046 a0001c0001t0001g0081 a0001c0001t0001g0083 others(116): Show |
122 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.2351+1289G>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 11/33 | chr2 | 201740385 | |||||||
| chr2:201740530 | T | A | 119 | a0001c0001t0001g0046 a0001c0001t0001g0081 a0001c0001t0001g0083 others(116): Show |
122 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.2351+1144A>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 11/33 | chr2 | 201740530 | |||||||
| chr2:201740536 | AAAC | A | 119 | a0001c0001t0001g0046 a0001c0001t0001g0081 a0001c0001t0001g0083 others(116): Show |
122 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.2351+1135_2351+113 others(7): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 11/33 | chr2 | 201740536 | |||||||
| chr2:201740612 | T | C | 1 | a0001c0001t0001g0206 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2351+1062A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 11/33 | chr2 | 201740612 | |||||||
| chr2:201740804 | G | A | 1 | a0001c0002t0001g0221 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2351+870C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 11/33 | chr2 | 201740804 | |||||||
| chr2:201740826 | C | G | 1 | a0001c0001t0001g0214 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2351+848G>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 11/33 | chr2 | 201740826 | |||||||
| chr2:201740939 | G | A | 11 | a0001c0002t0001g0092 a0001c0002t0001g0093 a0001c0002t0001g0096 others(8): Show |
11 | NA18951.hp1 NA18959.hp2 NA18961.hp2 others(8): Show |
intron_variant | MODIFIER | c.2351+735C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 11/33 | chr2 | 201740939 | |||||||
| chr2:201741024 | C | T | 1 | a0009c0016t0001g0130 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2351+650G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 11/33 | chr2 | 201741024 | |||||||
| chr2:201741084 | A | G | 1 | a0001c0003t0002g0179 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.2351+590T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 11/33 | chr2 | 201741084 | |||||||
| chr2:201741435 | C | T | 1 | a0001c0001t0001g0046 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2351+239G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 11/33 | chr2 | 201741435 | |||||||
| chr2:201741450 | T | C | 1 | a0001c0002t0001g0221 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2351+224A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 11/33 | chr2 | 201741450 | |||||||
| chr2:201741470 | C | T | 119 | a0001c0001t0001g0046 a0001c0001t0001g0081 a0001c0001t0001g0083 others(116): Show |
122 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.2351+204G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 11/33 | chr2 | 201741470 | |||||||
| chr2:201741867 | A | G | 1 | a0001c0003t0002g0179 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.2171-13T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 10/33 | chr2 | 201741867 | |||||||
| chr2:201741916 | G | A | 119 | a0001c0001t0001g0046 a0001c0001t0001g0081 a0001c0001t0001g0083 others(116): Show |
122 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.2171-62C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 10/33 | chr2 | 201741916 | |||||||
| chr2:201741935 | C | T | 1 | a0001c0002t0001g0108 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2171-81G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 10/33 | chr2 | 201741935 | |||||||
| chr2:201742035 | G | A | 5 | a0003c0007t0001g0034 a0003c0007t0001g0036 a0003c0007t0001g0037 others(2): Show |
5 | HG02258.hp1 HG02280.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.2171-181C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 10/33 | chr2 | 201742035 | |||||||
| chr2:201742081 | G | C | 1 | a0001c0002t0001g0039 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2171-227C>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 10/33 | chr2 | 201742081 | |||||||
| chr2:201742141 | G | A | 122 | a0001c0001t0001g0046 a0001c0001t0001g0081 a0001c0001t0001g0083 others(119): Show |
125 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.2171-287C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 10/33 | chr2 | 201742141 | |||||||
| chr2:201742403 | T | G | 120 | a0001c0001t0001g0046 a0001c0001t0001g0081 a0001c0001t0001g0083 others(117): Show |
123 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.2171-549A>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 10/33 | chr2 | 201742403 | |||||||
| chr2:201742420 | T | A | 12 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0022 others(9): Show |
12 | HG01109.hp2 HG01123.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.2171-566A>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 10/33 | chr2 | 201742420 | |||||||
| chr2:201742641 | G | C | 1 | a0004c0008t0001g0239 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.2171-787C>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 10/33 | chr2 | 201742641 | |||||||
| chr2:201742794 | G | A | 2 | a0001c0001t0001g0217 a0001c0004t0001g0216 |
2 | HG02027.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.2171-940C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 10/33 | chr2 | 201742794 | |||||||
| chr2:201742863 | G | A | 6 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0210 others(3): Show |
6 | HG02895.hp2 HG02897.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.2171-1009C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 10/33 | chr2 | 201742863 | |||||||
| chr2:201743010 | G | T | 1 | a0001c0001t0001g0318 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2171-1156C>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 10/33 | chr2 | 201743010 | |||||||
| chr2:201743019 | C | T | 1 | a0001c0001t0001g0038 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2171-1165G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 10/33 | chr2 | 201743019 | |||||||
| chr2:201743070 | C | CA | 113 | a0001c0001t0001g0081 a0001c0001t0001g0083 a0001c0001t0001g0149 others(110): Show |
115 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.2170+1187dupT | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 10/33 | chr2 | 201743070 | |||||||
| chr2:201743129 | C | T | 12 | a0001c0001t0001g0046 a0001c0004t0001g0004 a0001c0004t0001g0044 others(9): Show |
13 | HG00099.hp1 HG00642.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.2170+1129G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 10/33 | chr2 | 201743129 | |||||||
| chr2:201743133 | G | A | 2 | a0003c0007t0001g0032 a0003c0007t0001g0033 |
2 | HG01496.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.2170+1125C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 10/33 | chr2 | 201743133 | |||||||
| chr2:201743183 | G | C | 1 | a0004c0008t0001g0235 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.2170+1075C>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 10/33 | chr2 | 201743183 | |||||||
| chr2:201743410 | G | A | 9 | a0001c0001t0001g0205 a0001c0001t0001g0222 a0001c0001t0001g0227 others(6): Show |
10 | HG01515.hp2 HG01517.hp2 HG02004.hp2 others(7): Show |
intron_variant | MODIFIER | c.2170+848C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 10/33 | chr2 | 201743410 | |||||||
| chr2:201743486 | G | A | 12 | a0001c0001t0001g0046 a0001c0004t0001g0004 a0001c0004t0001g0044 others(9): Show |
13 | HG00099.hp1 HG00642.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.2170+772C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 10/33 | chr2 | 201743486 | |||||||
| chr2:201743534 | G | A | 1 | a0001c0001t0003g0023 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2170+724C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 10/33 | chr2 | 201743534 | |||||||
| chr2:201743609 | C | T | 1 | a0001c0001t0001g0205 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2170+649G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 10/33 | chr2 | 201743609 | |||||||
| chr2:201743610 | G | A | 9 | a0001c0001t0001g0237 a0001c0001t0001g0238 a0001c0001t0001g0241 others(6): Show |
9 | HG00597.hp1 HG00673.hp1 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.2170+648C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 10/33 | chr2 | 201743610 | |||||||
| chr2:201744154 | C | A | 124 | a0001c0001t0001g0038 a0001c0001t0001g0046 a0001c0001t0001g0081 others(121): Show |
127 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(124): Show |
intron_variant | MODIFIER | c.2170+104G>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 10/33 | chr2 | 201744154 | |||||||
| chr2:201744600 | C | G | 5 | a0003c0007t0001g0034 a0003c0007t0001g0036 a0003c0007t0001g0037 others(2): Show |
5 | HG02258.hp1 HG02280.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1999-171G>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 9/33 | chr2 | 201744600 | |||||||
| chr2:201744642 | G | A | 106 | a0001c0001t0001g0081 a0001c0001t0001g0083 a0001c0001t0001g0149 others(103): Show |
108 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.1999-213C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 9/33 | chr2 | 201744642 | |||||||
| chr2:201744787 | C | G | 1 | a0001c0003t0001g0042 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1999-358G>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 9/33 | chr2 | 201744787 | |||||||
| chr2:201745072 | G | A | 105 | a0001c0001t0001g0081 a0001c0001t0001g0083 a0001c0001t0001g0149 others(102): Show |
107 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.1999-643C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 9/33 | chr2 | 201745072 | |||||||
| chr2:201745127 | T | C | 3 | a0001c0002t0001g0089 a0001c0002t0001g0120 a0001c0002t0001g0121 |
3 | HG00733.hp2 HG01081.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.1999-698A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 9/33 | chr2 | 201745127 | |||||||
| chr2:201745273 | A | G | 1 | a0001c0001t0001g0038 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1999-844T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 9/33 | chr2 | 201745273 | |||||||
| chr2:201745425 | T | C | 1 | a0001c0001t0001g0038 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1999-996A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 9/33 | chr2 | 201745425 | |||||||
| chr2:201745521 | T | G | 109 | a0001c0001t0001g0081 a0001c0001t0001g0083 a0001c0001t0001g0149 others(106): Show |
111 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.1998+1045A>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 9/33 | chr2 | 201745521 | |||||||
| chr2:201745588 | A | G | 3 | a0002c0006t0001g0057 a0002c0006t0001g0058 a0002c0006t0001g0059 |
3 | HG00099.hp1 HG01081.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.1998+978T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 9/33 | chr2 | 201745588 | |||||||
| chr2:201745664 | T | C | 1 | a0001c0001t0001g0038 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1998+902A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 9/33 | chr2 | 201745664 | |||||||
| chr2:201745668 | G | A | 1 | a0001c0001t0001g0234 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1998+898C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 9/33 | chr2 | 201745668 | |||||||
| chr2:201745670 | C | T | 2 | a0003c0007t0001g0032 a0003c0007t0001g0033 |
2 | HG01496.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.1998+896G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 9/33 | chr2 | 201745670 | |||||||
| chr2:201745727 | T | C | 1 | a0001c0003t0002g0179 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1998+839A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 9/33 | chr2 | 201745727 | |||||||
| chr2:201745857 | G | A | 1 | a0002c0006t0005g0061 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1998+709C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 9/33 | chr2 | 201745857 | |||||||
| chr2:201745932 | G | A | 1 | a0001c0001t0001g0038 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1998+634C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 9/33 | chr2 | 201745932 | |||||||
| chr2:201745945 | T | C | 1 | a0001c0002t0001g0126 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1998+621A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 9/33 | chr2 | 201745945 | |||||||
| chr2:201745954 | A | G | 1 | a0001c0002t0001g0140 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1998+612T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 9/33 | chr2 | 201745954 | |||||||
| chr2:201745961 | T | A | 1 | a0001c0002t0001g0118 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1998+605A>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 9/33 | chr2 | 201745961 | |||||||
| chr2:201746155 | A | C | 1 | a0001c0001t0003g0020 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1998+411T>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 9/33 | chr2 | 201746155 | |||||||
| chr2:201746261 | T | C | 12 | a0001c0001t0001g0046 a0001c0004t0001g0004 a0001c0004t0001g0044 others(9): Show |
13 | HG00099.hp1 HG00642.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.1998+305A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 9/33 | chr2 | 201746261 | |||||||
| chr2:201746372 | T | C | 10 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0022 others(7): Show |
10 | HG01109.hp2 HG01123.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1998+194A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 9/33 | chr2 | 201746372 | |||||||
| chr2:201746415 | G | A | 1 | a0001c0001t0001g0281 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1998+151C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 9/33 | chr2 | 201746415 | |||||||
| chr2:201746440 | T | G | 2 | a0001c0001t0001g0217 a0001c0004t0001g0216 |
2 | HG02027.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.1998+126A>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 9/33 | chr2 | 201746440 | |||||||
| chr2:201746536 | T | C | 2 | a0001c0001t0003g0022 a0001c0004t0003g0029 |
2 | HG01109.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.1998+30A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 9/33 | chr2 | 201746536 | |||||||
| chr2:201746879 | C | A | 2 | a0001c0003t0002g0163 a0001c0003t0002g0187 |
2 | NA18959.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1816-131G>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 8/33 | chr2 | 201746879 | |||||||
| chr2:201747001 | A | G | 1 | a0011c0015t0002g0188 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1816-253T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 8/33 | chr2 | 201747001 | |||||||
| chr2:201747150 | C | T | 1 | a0001c0003t0001g0042 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1816-402G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 8/33 | chr2 | 201747150 | |||||||
| chr2:201747253 | C | T | 3 | a0001c0003t0002g0195 a0001c0003t0002g0196 a0001c0003t0002g0197 |
3 | NA18971.hp1 NA19004.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.1816-505G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 8/33 | chr2 | 201747253 | |||||||
| chr2:201747316 | G | A | 307 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(304): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.1816-568C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 8/33 | chr2 | 201747316 | |||||||
| chr2:201747364 | C | T | 5 | a0001c0001t0001g0015 a0001c0001t0001g0244 a0001c0001t0001g0265 others(2): Show |
6 | HG00438.hp1 HG02083.hp2 HG02129.hp1 others(3): Show |
intron_variant | MODIFIER | c.1816-616G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 8/33 | chr2 | 201747364 | |||||||
| chr2:201747456 | C | T | 9 | a0001c0002t0001g0092 a0001c0002t0001g0093 a0001c0002t0001g0096 others(6): Show |
9 | NA18951.hp1 NA18959.hp2 NA18961.hp2 others(6): Show |
intron_variant | MODIFIER | c.1816-708G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 8/33 | chr2 | 201747456 | |||||||
| chr2:201747462 | C | CT | 9 | a0001c0001t0001g0210 a0001c0001t0001g0252 a0001c0001t0001g0265 others(6): Show |
9 | HG02055.hp2 HG02486.hp1 HG03098.hp1 others(6): Show |
intron_variant | MODIFIER | c.1816-715dupA | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 8/33 | chr2 | 201747462 | |||||||
| chr2:201747462 | CT | C | 97 | a0001c0001t0001g0081 a0001c0001t0001g0083 a0001c0001t0001g0149 others(94): Show |
99 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.1816-715delA | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 8/33 | chr2 | 201747462 | |||||||
| chr2:201747672 | G | A | 1 | a0001c0001t0001g0244 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1816-924C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 8/33 | chr2 | 201747672 | |||||||
| chr2:201747725 | G | A | 241 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(238): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.1816-977C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 8/33 | chr2 | 201747725 | |||||||
| chr2:201747828 | A | G | 1 | a0001c0001t0001g0312 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1816-1080T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 8/33 | chr2 | 201747828 | |||||||
| chr2:201747865 | G | A | 327 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(324): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.1816-1117C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 8/33 | chr2 | 201747865 | |||||||
| chr2:201748049 | A | AAC | 13 | a0001c0001t0001g0206 a0001c0001t0003g0020 a0001c0001t0003g0021 others(10): Show |
13 | HG01109.hp2 HG01123.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1816-1303_1816-130 others(6): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 8/33 | chr2 | 201748049 | |||||||
| chr2:201748057 | C | T | 1 | a0001c0003t0002g0009 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1816-1309G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 8/33 | chr2 | 201748057 | |||||||
| chr2:201748204 | T | TTGTGTG | 4 | a0001c0003t0002g0175 a0001c0003t0002g0176 a0001c0003t0002g0177 others(1): Show |
4 | HG02071.hp2 HG02083.hp1 HG02135.hp1 others(1): Show |
intron_variant | MODIFIER | c.1816-1462_1816-145 others(10): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 8/33 | chr2 | 201748204 | |||||||
| chr2:201748370 | C | T | 327 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(324): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.1815+1342G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 8/33 | chr2 | 201748370 | |||||||
| chr2:201748650 | CTTTG | C | 120 | a0001c0001t0001g0038 a0001c0001t0001g0046 a0001c0001t0001g0081 others(117): Show |
123 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.1815+1058_1815+106 others(8): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 8/33 | chr2 | 201748650 | |||||||
| chr2:201748694 | C | T | 2 | a0003c0007t0001g0032 a0003c0007t0001g0033 |
2 | HG01496.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.1815+1018G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 8/33 | chr2 | 201748694 | |||||||
| chr2:201748713 | C | G | 1 | a0001c0001t0001g0208 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1815+999G>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 8/33 | chr2 | 201748713 | |||||||
| chr2:201748771 | T | C | 1 | a0001c0001t0001g0259 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1815+941A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 8/33 | chr2 | 201748771 | |||||||
| chr2:201748912 | C | T | 9 | a0001c0002t0001g0221 a0001c0002t0001g0223 a0001c0002t0001g0224 others(6): Show |
9 | HG00423.hp2 HG01069.hp2 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.1815+800G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 8/33 | chr2 | 201748912 | |||||||
| chr2:201748948 | G | A | 1 | a0001c0004t0001g0157 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1815+764C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 8/33 | chr2 | 201748948 | |||||||
| chr2:201748957 | C | G | 1 | a0001c0001t0001g0206 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1815+755G>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 8/33 | chr2 | 201748957 | |||||||
| chr2:201749057 | TGTTCAAG others(6): Show |
T | 2 | a0001c0001t0001g0242 a0001c0001t0001g0243 |
2 | HG02723.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1815+642_1815+654d others(15): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 8/33 | chr2 | 201749057 | |||||||
| chr2:201749218 | T | TA | 66 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0208 others(63): Show |
71 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.1815+493dupT | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 8/33 | chr2 | 201749218 | |||||||
| chr2:201749218 | TA | T | 117 | a0001c0001t0001g0046 a0001c0001t0001g0081 a0001c0001t0001g0083 others(114): Show |
120 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.1815+493delT | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 8/33 | chr2 | 201749218 | |||||||
| chr2:201749400 | C | T | 39 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(36): Show |
42 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.1815+312G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 8/33 | chr2 | 201749400 | |||||||
| chr2:201749496 | G | C | 107 | a0001c0001t0001g0081 a0001c0001t0001g0083 a0001c0001t0001g0149 others(104): Show |
109 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.1815+216C>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 8/33 | chr2 | 201749496 | |||||||
| chr2:201749555 | G | A | 1 | a0001c0001t0001g0038 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1815+157C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 8/33 | chr2 | 201749555 | |||||||
| chr2:201749605 | G | C | 1 | a0001c0001t0001g0243 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1815+107C>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 8/33 | chr2 | 201749605 | |||||||
| chr2:201749612 | G | A | 1 | a0001c0002t0001g0131 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1815+100C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 8/33 | chr2 | 201749612 | |||||||
| chr2:201749909 | T | C | 1 | a0001c0001t0001g0274 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1738-120A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 7/33 | chr2 | 201749909 | |||||||
| chr2:201749909 | T | G | 9 | a0001c0002t0001g0221 a0001c0002t0001g0223 a0001c0002t0001g0224 others(6): Show |
9 | HG00423.hp2 HG01069.hp2 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.1738-120A>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 7/33 | chr2 | 201749909 | |||||||
| chr2:201750168 | C | CA | 87 | a0001c0001t0001g0038 a0001c0001t0001g0207 a0001c0001t0001g0208 others(84): Show |
92 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.1738-380dupT | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 7/33 | chr2 | 201750168 | |||||||
| chr2:201750190 | AAAG | A | 39 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(36): Show |
42 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.1738-404_1738-402d others(5): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 7/33 | chr2 | 201750190 | |||||||
| chr2:201750201 | C | T | 1 | a0001c0001t0001g0038 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1738-412G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 7/33 | chr2 | 201750201 | |||||||
| chr2:201750591 | AG | A | 105 | a0001c0001t0001g0081 a0001c0001t0001g0083 a0001c0001t0001g0149 others(102): Show |
107 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.1738-803delC | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 7/33 | chr2 | 201750591 | |||||||
| chr2:201750607 | T | C | 12 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0022 others(9): Show |
12 | HG01109.hp2 HG01123.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1738-818A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 7/33 | chr2 | 201750607 | |||||||
| chr2:201750702 | A | G | 9 | a0001c0001t0001g0256 a0001c0001t0001g0269 a0001c0001t0001g0270 others(6): Show |
9 | HG00558.hp1 HG02015.hp1 NA18956.hp1 others(6): Show |
intron_variant | MODIFIER | c.1738-913T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 7/33 | chr2 | 201750702 | |||||||
| chr2:201750826 | G | A | 12 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0022 others(9): Show |
12 | HG01109.hp2 HG01123.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1738-1037C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 7/33 | chr2 | 201750826 | |||||||
| chr2:201750852 | C | CT | 8 | a0001c0001t0001g0237 a0001c0001t0001g0283 a0001c0001t0003g0022 others(5): Show |
8 | HG00597.hp1 HG01109.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.1738-1064dupA | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 7/33 | chr2 | 201750852 | |||||||
| chr2:201750883 | C | T | 1 | a0001c0001t0001g0273 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1738-1094G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 7/33 | chr2 | 201750883 | |||||||
| chr2:201751023 | C | T | 1 | a0001c0001t0001g0206 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1738-1234G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 7/33 | chr2 | 201751023 | |||||||
| chr2:201751496 | C | T | 118 | a0001c0001t0001g0046 a0001c0001t0001g0081 a0001c0001t0001g0083 others(115): Show |
121 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.1737+1650G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 7/33 | chr2 | 201751496 | |||||||
| chr2:201751606 | T | G | 3 | a0001c0003t0002g0165 a0001c0003t0002g0181 a0001c0003t0002g0182 |
3 | NA18980.hp1 NA18991.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1737+1540A>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 7/33 | chr2 | 201751606 | |||||||
| chr2:201751648 | G | A | 105 | a0001c0001t0001g0081 a0001c0001t0001g0083 a0001c0001t0001g0149 others(102): Show |
107 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.1737+1498C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 7/33 | chr2 | 201751648 | |||||||
| chr2:201751756 | C | T | 7 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0210 others(4): Show |
7 | HG01243.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1737+1390G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 7/33 | chr2 | 201751756 | |||||||
| chr2:201751785 | T | C | 1 | a0001c0002t0001g0139 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1737+1361A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 7/33 | chr2 | 201751785 | |||||||
| chr2:201751792 | T | C | 1 | a0001c0001t0001g0260 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1737+1354A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 7/33 | chr2 | 201751792 | |||||||
| chr2:201751823 | T | C | 5 | a0003c0007t0001g0034 a0003c0007t0001g0036 a0003c0007t0001g0037 others(2): Show |
5 | HG02258.hp1 HG02280.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1737+1323A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 7/33 | chr2 | 201751823 | |||||||
| chr2:201751973 | G | A | 1 | a0001c0001t0001g0282 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1737+1173C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 7/33 | chr2 | 201751973 | |||||||
| chr2:201752013 | A | C | 1 | a0001c0001t0001g0038 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1737+1133T>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 7/33 | chr2 | 201752013 | |||||||
| chr2:201752152 | T | C | 1 | a0002c0005t0001g0062 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1737+994A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 7/33 | chr2 | 201752152 | |||||||
| chr2:201752189 | C | T | 107 | a0001c0001t0001g0081 a0001c0001t0001g0083 a0001c0001t0001g0149 others(104): Show |
109 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.1737+957G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 7/33 | chr2 | 201752189 | |||||||
| chr2:201752528 | T | A | 11 | a0001c0004t0001g0006 a0001c0004t0001g0074 a0001c0004t0001g0075 others(8): Show |
12 | HG00642.hp2 HG01070.hp1 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.1737+618A>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 7/33 | chr2 | 201752528 | |||||||
| chr2:201752682 | C | T | 104 | a0001c0001t0001g0081 a0001c0001t0001g0083 a0001c0001t0001g0149 others(101): Show |
106 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.1737+464G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 7/33 | chr2 | 201752682 | |||||||
| chr2:201752788 | G | A | 1 | a0002c0006t0001g0059 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1737+358C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 7/33 | chr2 | 201752788 | |||||||
| chr2:201752975 | C | T | 2 | a0001c0001t0001g0327 a0001c0001t0001g0328 |
2 | NA18971.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.1737+171G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 7/33 | chr2 | 201752975 | |||||||
| chr2:201753071 | A | G | 1 | a0001c0002t0001g0039 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1737+75T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 7/33 | chr2 | 201753071 | |||||||
| chr2:201753087 | C | A | 1 | a0001c0001t0001g0238 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1737+59G>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 7/33 | chr2 | 201753087 | |||||||
| chr2:201753295 | G | A | 2 | a0001c0001t0001g0217 a0001c0004t0001g0216 |
2 | HG02027.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.1641-53C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 6/33 | chr2 | 201753295 | |||||||
| chr2:201753597 | C | G | 133 | a0001c0001t0001g0038 a0001c0001t0001g0046 a0001c0001t0001g0081 others(130): Show |
136 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.1641-355G>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 6/33 | chr2 | 201753597 | |||||||
| chr2:201753635 | C | A | 2 | a0001c0003t0002g0180 a0001c0003t0002g0183 |
2 | NA18940.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1641-393G>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 6/33 | chr2 | 201753635 | |||||||
| chr2:201754020 | T | C | 1 | a0001c0001t0001g0038 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1640+483A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 6/33 | chr2 | 201754020 | |||||||
| chr2:201754142 | A | G | 2 | a0001c0001t0001g0217 a0001c0004t0001g0216 |
2 | HG02027.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.1640+361T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 6/33 | chr2 | 201754142 | |||||||
| chr2:201754349 | G | C | 5 | a0003c0007t0001g0034 a0003c0007t0001g0036 a0003c0007t0001g0037 others(2): Show |
5 | HG02258.hp1 HG02280.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1640+154C>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 6/33 | chr2 | 201754349 | |||||||
| chr2:201754452 | G | C | 4 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0297 others(1): Show |
5 | HG01515.hp2 HG01517.hp2 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.1640+51C>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 6/33 | chr2 | 201754452 | |||||||
| chr2:201754817 | G | T | 4 | a0001c0001t0001g0283 a0001c0001t0001g0284 a0001c0001t0001g0285 others(1): Show |
4 | NA18942.hp1 NA18951.hp2 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.1472-146C>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 5/33 | chr2 | 201754817 | |||||||
| chr2:201754859 | A | C | 2 | a0001c0003t0007g0040 a0001c0003t0007g0041 |
2 | HG02622.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1472-188T>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 5/33 | chr2 | 201754859 | |||||||
| chr2:201754905 | G | C | 1 | a0001c0001t0003g0022 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1472-234C>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 5/33 | chr2 | 201754905 | |||||||
| chr2:201755115 | G | A | 1 | a0001c0011t0001g0084 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1472-444C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 5/33 | chr2 | 201755115 | |||||||
| chr2:201755162 | G | A | 8 | a0001c0002t0001g0085 a0001c0002t0001g0089 a0001c0002t0001g0120 others(5): Show |
8 | HG00733.hp2 HG00738.hp1 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.1472-491C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 5/33 | chr2 | 201755162 | |||||||
| chr2:201755266 | C | CT | 7 | a0003c0007t0001g0032 a0003c0007t0001g0033 a0003c0007t0001g0034 others(4): Show |
7 | HG01496.hp2 HG02258.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1472-596dupA | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 5/33 | chr2 | 201755266 | |||||||
| chr2:201755365 | T | C | 104 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(101): Show |
115 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.1472-694A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 5/33 | chr2 | 201755365 | |||||||
| chr2:201755380 | A | G | 2 | a0001c0001t0001g0255 a0001c0001t0001g0282 |
2 | HG02602.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1472-709T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 5/33 | chr2 | 201755380 | |||||||
| chr2:201755396 | A | G | 104 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(101): Show |
115 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.1472-725T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 5/33 | chr2 | 201755396 | |||||||
| chr2:201755511 | C | T | 1 | a0001c0002t0001g0232 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1472-840G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 5/33 | chr2 | 201755511 | |||||||
| chr2:201755705 | A | G | 2 | a0001c0001t0001g0217 a0001c0004t0001g0216 |
2 | HG02027.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.1472-1034T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 5/33 | chr2 | 201755705 | |||||||
| chr2:201755733 | A | C | 2 | a0001c0001t0001g0280 a0001c0001t0001g0281 |
2 | HG02735.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1472-1062T>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 5/33 | chr2 | 201755733 | |||||||
| chr2:201755833 | T | C | 7 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0210 others(4): Show |
7 | HG01243.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1472-1162A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 5/33 | chr2 | 201755833 | |||||||
| chr2:201756051 | A | C | 1 | a0001c0002t0001g0123 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1471+1351T>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 5/33 | chr2 | 201756051 | |||||||
| chr2:201756074 | C | T | 1 | a0001c0001t0001g0206 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1471+1328G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 5/33 | chr2 | 201756074 | |||||||
| chr2:201756111 | T | C | 43 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(40): Show |
46 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.1471+1291A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 5/33 | chr2 | 201756111 | |||||||
| chr2:201756265 | T | C | 104 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(101): Show |
115 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.1471+1137A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 5/33 | chr2 | 201756265 | |||||||
| chr2:201756279 | T | C | 111 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(108): Show |
122 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.1471+1123A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 5/33 | chr2 | 201756279 | |||||||
| chr2:201756318 | A | G | 104 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(101): Show |
115 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.1471+1084T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 5/33 | chr2 | 201756318 | |||||||
| chr2:201756377 | A | G | 1 | a0001c0001t0001g0234 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1471+1025T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 5/33 | chr2 | 201756377 | |||||||
| chr2:201756430 | A | C | 1 | a0001c0003t0002g0199 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1471+972T>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 5/33 | chr2 | 201756430 | |||||||
| chr2:201756467 | C | T | 1 | a0001c0001t0001g0206 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1471+935G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 5/33 | chr2 | 201756467 | |||||||
| chr2:201756525 | T | C | 13 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(10): Show |
16 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(13): Show |
intron_variant | MODIFIER | c.1471+877A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 5/33 | chr2 | 201756525 | |||||||
| chr2:201756593 | A | G | 104 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(101): Show |
115 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.1471+809T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 5/33 | chr2 | 201756593 | |||||||
| chr2:201756649 | T | C | 13 | a0001c0001t0001g0256 a0001c0001t0001g0269 a0001c0001t0001g0270 others(10): Show |
13 | HG00558.hp1 HG00621.hp1 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.1471+753A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 5/33 | chr2 | 201756649 | |||||||
| chr2:201756684 | A | C | 1 | a0001c0001t0008g0279 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1471+718T>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 5/33 | chr2 | 201756684 | |||||||
| chr2:201756746 | T | C | 1 | a0001c0002t0001g0128 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1471+656A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 5/33 | chr2 | 201756746 | |||||||
| chr2:201756801 | T | G | 1 | a0001c0001t0001g0238 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1471+601A>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 5/33 | chr2 | 201756801 | |||||||
| chr2:201756812 | A | G | 1 | a0001c0001t0001g0238 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1471+590T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 5/33 | chr2 | 201756812 | |||||||
| chr2:201756816 | C | T | 1 | a0001c0001t0001g0245 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1471+586G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 5/33 | chr2 | 201756816 | |||||||
| chr2:201756901 | AT | A | 112 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(109): Show |
123 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.1471+500delA | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 5/33 | chr2 | 201756901 | |||||||
| chr2:201756964 | T | C | 1 | a0002c0020t0001g0063 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1471+438A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 5/33 | chr2 | 201756964 | |||||||
| chr2:201756978 | T | C | 1 | a0001c0001t0001g0323 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1471+424A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 5/33 | chr2 | 201756978 | |||||||
| chr2:201757017 | G | A | 1 | a0002c0020t0001g0063 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1471+385C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 5/33 | chr2 | 201757017 | |||||||
| chr2:201757053 | C | G | 1 | a0001c0001t0001g0038 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1471+349G>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 5/33 | chr2 | 201757053 | |||||||
| chr2:201757169 | A | G | 1 | a0001c0001t0001g0308 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1471+233T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 5/33 | chr2 | 201757169 | |||||||
| chr2:201757370 | A | G | 1 | a0001c0001t0001g0278 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1471+32T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 5/33 | chr2 | 201757370 | |||||||
| chr2:201757396 | C | T | 1 | a0001c0001t0001g0277 | 1 | NA19081.hp1 | splice_region_variant&intron_variant | LOW | c.1471+6G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 5/33 | chr2 | 201757396 | |||||||
| chr2:201757786 | T | C | 104 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(101): Show |
115 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.1114-27A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201757786 | |||||||
| chr2:201758128 | C | T | 2 | a0001c0001t0001g0275 a0001c0001t0001g0276 |
2 | NA19057.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1114-369G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201758128 | |||||||
| chr2:201758243 | T | C | 104 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(101): Show |
115 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.1114-484A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201758243 | |||||||
| chr2:201758285 | G | A | 104 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(101): Show |
115 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.1114-526C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201758285 | |||||||
| chr2:201758342 | C | T | 201 | a0001c0001t0001g0046 a0001c0001t0001g0081 a0001c0001t0001g0083 others(198): Show |
210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.1114-583G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201758342 | |||||||
| chr2:201758588 | A | C | 1 | a0010c0014t0001g0043 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1114-829T>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201758588 | |||||||
| chr2:201758643 | C | A | 1 | a0001c0001t0001g0205 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1114-884G>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201758643 | |||||||
| chr2:201758653 | C | T | 1 | a0001c0003t0002g0186 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1114-894G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201758653 | |||||||
| chr2:201758681 | C | T | 7 | a0003c0007t0001g0032 a0003c0007t0001g0033 a0003c0007t0001g0034 others(4): Show |
7 | HG01496.hp2 HG02258.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1114-922G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201758681 | |||||||
| chr2:201758732 | A | G | 1 | a0001c0001t0001g0274 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1114-973T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201758732 | |||||||
| chr2:201758740 | TATA | T | 13 | a0002c0005t0001g0002 a0002c0005t0001g0005 a0002c0005t0001g0056 others(10): Show |
16 | HG00099.hp1 HG01074.hp1 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.1114-984_1114-982d others(5): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201758740 | |||||||
| chr2:201758755 | T | TGC | 6 | a0001c0002t0001g0085 a0001c0002t0001g0086 a0001c0002t0001g0141 others(3): Show |
6 | HG03209.hp2 HG04115.hp1 NA18941.hp1 others(3): Show |
intron_variant | MODIFIER | c.1114-998_1114-997d others(4): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201758755 | |||||||
| chr2:201758755 | T | TGCGC | 3 | a0001c0002t0001g0091 a0001c0002t0001g0123 a0001c0004t0001g0157 |
3 | HG01517.hp1 HG01884.hp1 HG02015.hp2 |
intron_variant | MODIFIER | c.1114-1000_1114-997 others(7): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201758755 | |||||||
| chr2:201758759 | C | CGCGT | 98 | a0001c0001t0001g0081 a0001c0001t0001g0083 a0001c0001t0001g0149 others(95): Show |
100 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.1114-1001_1114-100 others(8): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201758759 | |||||||
| chr2:201758760 | A | ATG | 22 | a0001c0001t0001g0038 a0001c0001t0001g0206 a0001c0001t0003g0020 others(19): Show |
23 | HG00642.hp1 HG00738.hp2 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.1114-1003_1114-100 others(6): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201758760 | |||||||
| chr2:201758760 | A | ATGTGTG | 3 | a0001c0001t0003g0023 a0001c0001t0006g0330 a0001c0001t0006g0331 |
3 | HG03098.hp2 HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1114-1007_1114-100 others(10): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201758760 | |||||||
| chr2:201758760 | A | ATGTGTGT others(1): Show |
3 | a0001c0001t0001g0014 a0001c0001t0001g0244 a0001c0001t0001g0254 |
4 | NA18949.hp2 NA18968.hp2 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.1114-1009_1114-100 others(12): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201758760 | |||||||
| chr2:201758760 | A | ATGTGTGT others(3): Show |
95 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(92): Show |
105 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.1114-1011_1114-100 others(14): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201758760 | |||||||
| chr2:201758760 | A | ATGTGTGT others(5): Show |
2 | a0001c0001t0001g0262 a0001c0001t0001g0263 |
2 | HG02717.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1114-1013_1114-100 others(16): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201758760 | |||||||
| chr2:201758760 | A | ATGTGTGT others(7): Show |
2 | a0001c0001t0001g0302 a0001c0001t0001g0313 |
2 | HG03491.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.1114-1015_1114-100 others(18): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201758760 | |||||||
| chr2:201758760 | A | ATTGTGTG others(4): Show |
1 | a0001c0001t0001g0320 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1114-1002_1114-100 others(15): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201758760 | |||||||
| chr2:201758760 | A | G | 175 | a0001c0001t0001g0081 a0001c0001t0001g0083 a0001c0001t0001g0149 others(172): Show |
183 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.1114-1001T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201758760 | |||||||
| chr2:201758761 | T | C | 62 | a0001c0001t0001g0205 a0001c0001t0001g0208 a0001c0001t0001g0209 others(59): Show |
68 | HG00544.hp1 HG00597.hp2 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.1114-1002A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201758761 | |||||||
| chr2:201758763 | T | C | 9 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0210 others(6): Show |
9 | HG01243.hp2 HG02895.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.1114-1004A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201758763 | |||||||
| chr2:201758785 | T | TGTGTGTG others(4): Show |
1 | a0001c0001t0001g0247 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1114-1027_1114-102 others(15): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201758785 | |||||||
| chr2:201758786 | T | G | 9 | a0001c0001t0001g0038 a0001c0003t0002g0160 a0003c0007t0001g0032 others(6): Show |
9 | HG01496.hp2 HG02258.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1114-1027A>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201758786 | |||||||
| chr2:201758862 | G | T | 1 | a0001c0001t0001g0234 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1114-1103C>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201758862 | |||||||
| chr2:201758919 | T | A | 9 | a0001c0001t0001g0046 a0001c0004t0001g0004 a0001c0004t0001g0044 others(6): Show |
10 | HG00642.hp1 HG00738.hp2 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1114-1160A>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201758919 | |||||||
| chr2:201758923 | A | G | 1 | a0001c0001t0001g0253 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1114-1164T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201758923 | |||||||
| chr2:201758971 | A | C | 2 | a0001c0001t0001g0242 a0001c0001t0001g0243 |
2 | HG02723.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1114-1212T>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201758971 | |||||||
| chr2:201758977 | T | C | 1 | a0001c0004t0001g0157 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1114-1218A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201758977 | |||||||
| chr2:201759221 | T | C | 1 | a0001c0002t0001g0123 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1114-1462A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201759221 | |||||||
| chr2:201759296 | A | C | 2 | a0001c0009t0001g0016 a0001c0009t0001g0311 |
3 | HG00280.hp2 HG00323.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.1114-1537T>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201759296 | |||||||
| chr2:201759344 | C | T | 1 | a0001c0001t0001g0038 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1113+1537G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201759344 | |||||||
| chr2:201759413 | T | C | 1 | a0002c0006t0005g0061 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1113+1468A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201759413 | |||||||
| chr2:201759415 | T | C | 1 | a0002c0005t0001g0067 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1113+1466A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201759415 | |||||||
| chr2:201759587 | A | G | 1 | a0001c0001t0001g0256 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1113+1294T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201759587 | |||||||
| chr2:201759604 | A | G | 1 | a0002c0020t0001g0063 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1113+1277T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201759604 | |||||||
| chr2:201760043 | C | T | 1 | a0001c0003t0002g0185 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1113+838G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201760043 | |||||||
| chr2:201760244 | G | A | 1 | a0001c0004t0001g0050 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1113+637C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201760244 | |||||||
| chr2:201760250 | G | A | 1 | a0001c0001t0001g0272 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1113+631C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201760250 | |||||||
| chr2:201760295 | A | G | 1 | a0001c0004t0001g0216 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1113+586T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201760295 | |||||||
| chr2:201760380 | A | G | 1 | a0001c0003t0004g0154 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1113+501T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201760380 | |||||||
| chr2:201760395 | T | G | 3 | a0001c0001t0003g0021 a0001c0001t0003g0024 a0001c0001t0003g0025 |
3 | HG01123.hp1 HG02622.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1113+486A>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201760395 | |||||||
| chr2:201760574 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1113+307G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201760574 | |||||||
| chr2:201760659 | T | C | 1 | a0001c0003t0002g0193 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1113+222A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201760659 | |||||||
| chr2:201760679 | A | C | 7 | a0003c0007t0001g0032 a0003c0007t0001g0033 a0003c0007t0001g0034 others(4): Show |
7 | HG01496.hp2 HG02258.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1113+202T>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201760679 | |||||||
| chr2:201760796 | G | A | 1 | a0004c0008t0001g0240 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1113+85C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 4/33 | chr2 | 201760796 | |||||||
| chr2:201761897 | C | T | 1 | a0001c0001t0001g0038 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.176-79G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201761897 | |||||||
| chr2:201761902 | A | C | 104 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(101): Show |
115 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.176-84T>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201761902 | |||||||
| chr2:201762057 | G | A | 1 | a0001c0001t0003g0031 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.176-239C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201762057 | |||||||
| chr2:201762124 | C | T | 1 | a0001c0002t0001g0098 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.176-306G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201762124 | |||||||
| chr2:201762296 | G | A | 104 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(101): Show |
115 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.176-478C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201762296 | |||||||
| chr2:201762500 | G | T | 1 | a0001c0002t0001g0134 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.176-682C>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201762500 | |||||||
| chr2:201762636 | G | A | 12 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0022 others(9): Show |
12 | HG01109.hp2 HG01123.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.176-818C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201762636 | |||||||
| chr2:201762781 | A | G | 104 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(101): Show |
115 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.176-963T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201762781 | |||||||
| chr2:201762854 | C | T | 2 | a0001c0001t0006g0330 a0001c0001t0006g0331 |
2 | HG03098.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.176-1036G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201762854 | |||||||
| chr2:201762940 | G | A | 1 | a0001c0001t0001g0247 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.176-1122C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201762940 | |||||||
| chr2:201762992 | T | C | 1 | a0001c0002t0001g0125 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.176-1174A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201762992 | |||||||
| chr2:201763066 | G | C | 1 | a0001c0001t0001g0301 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.176-1248C>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201763066 | |||||||
| chr2:201763068 | C | G | 2 | a0001c0004t0001g0044 a0001c0004t0001g0045 |
2 | HG02615.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.176-1250G>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201763068 | |||||||
| chr2:201763120 | T | G | 1 | a0001c0001t0001g0207 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.176-1302A>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201763120 | |||||||
| chr2:201763142 | G | A | 1 | a0001c0002t0001g0126 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.176-1324C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201763142 | |||||||
| chr2:201763194 | G | A | 7 | a0003c0007t0001g0032 a0003c0007t0001g0033 a0003c0007t0001g0034 others(4): Show |
7 | HG01496.hp2 HG02258.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.176-1376C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201763194 | |||||||
| chr2:201763207 | G | A | 9 | a0001c0001t0001g0046 a0001c0004t0001g0004 a0001c0004t0001g0044 others(6): Show |
10 | HG00642.hp1 HG00738.hp2 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.176-1389C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201763207 | |||||||
| chr2:201763237 | T | C | 48 | a0001c0001t0001g0207 a0001c0003t0001g0172 a0001c0003t0002g0003 others(45): Show |
53 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.176-1419A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201763237 | |||||||
| chr2:201763285 | T | C | 2 | a0001c0001t0001g0302 a0001c0001t0001g0313 |
2 | HG03491.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.176-1467A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201763285 | |||||||
| chr2:201763351 | C | T | 1 | a0001c0001t0003g0020 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.176-1533G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201763351 | |||||||
| chr2:201763508 | C | T | 1 | a0001c0002t0001g0233 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.176-1690G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201763508 | |||||||
| chr2:201763557 | T | C | 314 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(311): Show |
334 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(331): Show |
intron_variant | MODIFIER | c.176-1739A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201763557 | |||||||
| chr2:201763742 | C | T | 314 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(311): Show |
334 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(331): Show |
intron_variant | MODIFIER | c.176-1924G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201763742 | |||||||
| chr2:201763871 | A | T | 1 | a0001c0001t0001g0205 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.176-2053T>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201763871 | |||||||
| chr2:201763924 | T | G | 104 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(101): Show |
115 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.176-2106A>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201763924 | |||||||
| chr2:201764026 | A | G | 1 | a0001c0001t0001g0273 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.176-2208T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201764026 | |||||||
| chr2:201764044 | C | G | 1 | a0001c0002t0001g0089 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.176-2226G>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201764044 | |||||||
| chr2:201764098 | C | G | 314 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(311): Show |
334 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(331): Show |
intron_variant | MODIFIER | c.176-2280G>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201764098 | |||||||
| chr2:201764266 | C | T | 3 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0212 |
3 | HG02922.hp2 HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.176-2448G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201764266 | |||||||
| chr2:201764413 | C | A | 1 | a0014c0017t0001g0228 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.176-2595G>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201764413 | |||||||
| chr2:201764475 | C | CAA | 104 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(101): Show |
115 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.176-2659_176-2658d others(4): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201764475 | |||||||
| chr2:201764529 | G | A | 104 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(101): Show |
115 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.175+2700C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201764529 | |||||||
| chr2:201764629 | G | A | 2 | a0001c0002t0001g0094 a0001c0002t0001g0095 |
2 | NA18988.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.175+2600C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201764629 | |||||||
| chr2:201764634 | A | AAAAT | 41 | a0001c0001t0001g0046 a0001c0001t0001g0081 a0001c0001t0001g0208 others(38): Show |
41 | HG00140.hp2 HG00323.hp1 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.175+2591_175+2594d others(6): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201764634 | |||||||
| chr2:201764634 | A | AAAATAAA others(1): Show |
8 | a0001c0001t0001g0149 a0001c0002t0001g0131 a0001c0003t0002g0220 others(5): Show |
8 | HG00140.hp1 HG01175.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.175+2587_175+2594d others(10): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201764634 | |||||||
| chr2:201764634 | A | AAAATAAA others(5): Show |
1 | a0001c0011t0001g0084 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.175+2583_175+2594d others(14): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201764634 | |||||||
| chr2:201764634 | AAAAT | A | 91 | a0001c0001t0001g0015 a0001c0001t0001g0205 a0001c0001t0001g0207 others(88): Show |
101 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.175+2591_175+2594d others(6): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201764634 | |||||||
| chr2:201764634 | AAAATAAA others(1): Show |
A | 83 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0017 others(80): Show |
91 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.175+2587_175+2594d others(10): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201764634 | |||||||
| chr2:201764634 | AAAATAAA others(5): Show |
A | 1 | a0001c0001t0001g0303 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.175+2583_175+2594d others(14): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201764634 | |||||||
| chr2:201764686 | A | T | 7 | a0001c0004t0001g0004 a0001c0004t0001g0048 a0001c0004t0001g0049 others(4): Show |
8 | HG00642.hp1 HG00738.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.175+2543T>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201764686 | |||||||
| chr2:201764705 | T | G | 1 | a0001c0001t0001g0315 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.175+2524A>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201764705 | |||||||
| chr2:201764709 | T | C | 4 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(1): Show |
4 | NA18956.hp1 NA18994.hp1 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.175+2520A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201764709 | |||||||
| chr2:201764764 | T | C | 1 | a0001c0002t0001g0307 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.175+2465A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201764764 | |||||||
| chr2:201764864 | G | A | 3 | a0001c0003t0002g0195 a0001c0003t0002g0196 a0001c0003t0002g0197 |
3 | NA18971.hp1 NA19004.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.175+2365C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201764864 | |||||||
| chr2:201764906 | T | C | 5 | a0001c0003t0002g0165 a0001c0003t0002g0180 a0001c0003t0002g0181 others(2): Show |
5 | NA18940.hp1 NA18980.hp1 NA18991.hp2 others(2): Show |
intron_variant | MODIFIER | c.175+2323A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201764906 | |||||||
| chr2:201764997 | C | CT | 9 | a0001c0001t0001g0205 a0001c0003t0004g0154 a0001c0004t0001g0006 others(6): Show |
10 | HG00642.hp2 HG01070.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.175+2231dupA | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201764997 | |||||||
| chr2:201765102 | A | C | 1 | a0001c0003t0002g0184 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.175+2127T>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201765102 | |||||||
| chr2:201765276 | C | T | 2 | a0007c0010t0001g0097 a0007c0010t0001g0145 |
2 | NA19005.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.175+1953G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201765276 | |||||||
| chr2:201765645 | A | ATACTT | 17 | a0001c0001t0001g0081 a0001c0001t0001g0083 a0001c0001t0001g0222 others(14): Show |
17 | HG00140.hp1 HG00423.hp2 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.175+1579_175+1583d others(7): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201765645 | |||||||
| chr2:201765701 | G | A | 104 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(101): Show |
115 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.175+1528C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201765701 | |||||||
| chr2:201765753 | T | G | 2 | a0001c0001t0001g0217 a0001c0004t0001g0216 |
2 | HG02027.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.175+1476A>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201765753 | |||||||
| chr2:201765790 | T | C | 104 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(101): Show |
115 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.175+1439A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201765790 | |||||||
| chr2:201765915 | G | A | 15 | a0002c0005t0001g0002 a0002c0005t0001g0005 a0002c0005t0001g0056 others(12): Show |
18 | HG00099.hp1 HG01074.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.175+1314C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201765915 | |||||||
| chr2:201766102 | T | C | 104 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(101): Show |
115 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.175+1127A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201766102 | |||||||
| chr2:201766108 | T | G | 1 | a0001c0002t0001g0143 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.175+1121A>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201766108 | |||||||
| chr2:201766235 | A | C | 3 | a0001c0003t0004g0154 a0001c0003t0004g0155 a0001c0003t0004g0156 |
3 | HG00741.hp1 HG01099.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.175+994T>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201766235 | |||||||
| chr2:201766694 | C | A | 112 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(109): Show |
123 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.175+535G>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201766694 | |||||||
| chr2:201766722 | G | GAAAATGT others(314): Show |
1 | a0001c0001t0001g0206 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.175+506_175+507ins others(321): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201766722 | |||||||
| chr2:201766722 | G | GAAAATGT others(302): Show |
1 | a0001c0002t0001g0223 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.175+506_175+507ins others(309): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201766722 | |||||||
| chr2:201766722 | G | GAAAATGT others(312): Show |
1 | a0001c0003t0002g0193 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.175+506_175+507ins others(319): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201766722 | |||||||
| chr2:201766722 | G | GAAAATGT others(313): Show |
40 | a0001c0001t0001g0207 a0001c0002t0001g0096 a0001c0002t0001g0224 others(37): Show |
44 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.175+506_175+507ins others(320): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201766722 | |||||||
| chr2:201766722 | G | GAAAATGT others(314): Show |
92 | a0001c0001t0001g0083 a0001c0001t0001g0149 a0001c0001t0001g0205 others(89): Show |
95 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.175+506_175+507ins others(321): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201766722 | |||||||
| chr2:201766722 | G | GAAAATGT others(315): Show |
37 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0210 others(34): Show |
38 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(35): Show |
intron_variant | MODIFIER | c.175+506_175+507ins others(322): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201766722 | |||||||
| chr2:201766722 | G | GAAAATGT others(316): Show |
3 | a0001c0002t0001g0142 a0001c0002t0001g0143 a0001c0003t0001g0042 |
3 | HG00741.hp2 HG02486.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.175+506_175+507ins others(323): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201766722 | |||||||
| chr2:201766722 | G | GAAAATGT others(315): Show |
1 | a0001c0001t0001g0081 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.175+506_175+507ins others(322): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201766722 | |||||||
| chr2:201766727 | T | TGTGGCAC others(315): Show |
1 | a0001c0002t0001g0144 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.175+501_175+502ins others(322): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201766727 | |||||||
| chr2:201766751 | A | G | 1 | a0001c0001t0001g0326 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.175+478T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201766751 | |||||||
| chr2:201766768 | A | G | 7 | a0003c0007t0001g0032 a0003c0007t0001g0033 a0003c0007t0001g0034 others(4): Show |
7 | HG01496.hp2 HG02258.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.175+461T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201766768 | |||||||
| chr2:201766854 | ACACCGCA others(6): Show |
A | 1 | a0001c0001t0001g0206 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.175+362_175+374del others(13): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201766854 | |||||||
| chr2:201766874 | T | C | 2 | a0001c0001t0001g0217 a0001c0004t0001g0216 |
2 | HG02027.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.175+355A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201766874 | |||||||
| chr2:201766889 | A | C | 1 | a0001c0001t0001g0206 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.175+340T>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201766889 | |||||||
| chr2:201766892 | C | T | 320 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(317): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.175+337G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201766892 | |||||||
| chr2:201766956 | C | G | 136 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(133): Show |
151 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.175+273G>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201766956 | |||||||
| chr2:201766978 | A | G | 48 | a0001c0001t0001g0207 a0001c0003t0001g0172 a0001c0003t0002g0003 others(45): Show |
53 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.175+251T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201766978 | |||||||
| chr2:201766990 | C | T | 7 | a0003c0007t0001g0032 a0003c0007t0001g0033 a0003c0007t0001g0034 others(4): Show |
7 | HG01496.hp2 HG02258.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.175+239G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201766990 | |||||||
| chr2:201767034 | T | A | 1 | a0001c0004t0001g0079 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.175+195A>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201767034 | |||||||
| chr2:201767058 | G | A | 2 | a0001c0002t0001g0230 a0001c0002t0001g0231 |
2 | HG01934.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.175+171C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201767058 | |||||||
| chr2:201767106 | A | T | 1 | a0001c0011t0001g0084 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.175+123T>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201767106 | |||||||
| chr2:201767201 | G | A | 3 | a0001c0001t0001g0217 a0001c0001t0001g0308 a0001c0004t0001g0216 |
3 | HG02027.hp2 NA19060.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.175+28C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 3/33 | chr2 | 201767201 | |||||||
| chr2:201767559 | A | G | 9 | a0001c0001t0001g0046 a0001c0004t0001g0004 a0001c0004t0001g0044 others(6): Show |
10 | HG00642.hp1 HG00738.hp2 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.21-176T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 2/33 | chr2 | 201767559 | |||||||
| chr2:201767572 | A | T | 2 | a0001c0001t0006g0330 a0001c0001t0006g0331 |
2 | HG03098.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.21-189T>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 2/33 | chr2 | 201767572 | |||||||
| chr2:201767588 | C | T | 14 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0022 others(11): Show |
14 | HG01109.hp2 HG01123.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.21-205G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 2/33 | chr2 | 201767588 | |||||||
| chr2:201767611 | C | T | 2 | a0001c0003t0002g0167 a0001c0003t0002g0198 |
2 | NA18981.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.21-228G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 2/33 | chr2 | 201767611 | |||||||
| chr2:201767629 | G | A | 2 | a0001c0001t0006g0330 a0001c0001t0006g0331 |
2 | HG03098.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.21-246C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 2/33 | chr2 | 201767629 | |||||||
| chr2:201767639 | G | A | 1 | a0001c0001t0001g0038 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.21-256C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 2/33 | chr2 | 201767639 | |||||||
| chr2:201767677 | C | T | 320 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(317): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.21-294G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 2/33 | chr2 | 201767677 | |||||||
| chr2:201767705 | C | CAA | 100 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(97): Show |
111 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.21-324_21-323dupTT | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 2/33 | chr2 | 201767705 | |||||||
| chr2:201767705 | CA | C | 7 | a0003c0007t0001g0032 a0003c0007t0001g0033 a0003c0007t0001g0034 others(4): Show |
7 | HG01496.hp2 HG02258.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.21-323delT | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 2/33 | chr2 | 201767705 | |||||||
| chr2:201767707 | A | C | 2 | a0001c0002t0001g0094 a0001c0002t0001g0095 |
2 | NA18988.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.21-324T>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 2/33 | chr2 | 201767707 | |||||||
| chr2:201767782 | C | T | 14 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0022 others(11): Show |
14 | HG01109.hp2 HG01123.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.21-399G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 2/33 | chr2 | 201767782 | |||||||
| chr2:201767866 | T | A | 2 | a0001c0004t0001g0074 a0001c0004t0001g0075 |
2 | HG02293.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.21-483A>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 2/33 | chr2 | 201767866 | |||||||
| chr2:201767866 | T | TA | 93 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(90): Show |
104 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.21-484dupT | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 2/33 | chr2 | 201767866 | |||||||
| chr2:201767866 | T | TAA | 11 | a0001c0001t0001g0241 a0001c0001t0001g0248 a0001c0001t0001g0253 others(8): Show |
11 | HG00438.hp1 HG00673.hp1 HG02056.hp1 others(8): Show |
intron_variant | MODIFIER | c.21-485_21-484dupTT | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 2/33 | chr2 | 201767866 | |||||||
| chr2:201767866 | TA | T | 137 | a0001c0001t0001g0038 a0001c0001t0001g0046 a0001c0001t0001g0081 others(134): Show |
140 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.21-484delT | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 2/33 | chr2 | 201767866 | |||||||
| chr2:201767866 | TAA | T | 49 | a0001c0001t0001g0207 a0001c0002t0001g0092 a0001c0002t0001g0093 others(46): Show |
53 | HG00423.hp1 HG00597.hp2 HG01168.hp1 others(50): Show |
intron_variant | MODIFIER | c.21-485_21-484delTT | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 2/33 | chr2 | 201767866 | |||||||
| chr2:201768057 | A | C | 67 | a0001c0001t0001g0205 a0001c0001t0001g0207 a0001c0001t0001g0208 others(64): Show |
73 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.21-674T>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 2/33 | chr2 | 201768057 | |||||||
| chr2:201768158 | A | G | 2 | a0001c0001t0006g0330 a0001c0001t0006g0331 |
2 | HG03098.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.20+708T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 2/33 | chr2 | 201768158 | |||||||
| chr2:201768215 | T | C | 177 | a0001c0001t0001g0081 a0001c0001t0001g0083 a0001c0001t0001g0149 others(174): Show |
185 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.20+651A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 2/33 | chr2 | 201768215 | |||||||
| chr2:201768249 | C | T | 1 | a0001c0002t0001g0052 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.20+617G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 2/33 | chr2 | 201768249 | |||||||
| chr2:201768638 | A | T | 1 | a0001c0001t0001g0255 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.20+228T>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 2/33 | chr2 | 201768638 | |||||||
| chr2:201768744 | T | C | 1 | a0001c0001t0003g0031 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.20+122A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 2/33 | chr2 | 201768744 | |||||||
| chr2:201768859 | A | G | 104 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(101): Show |
115 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(112): Show |
splice_region_variant&intron_variant | LOW | c.20+7T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 2/33 | chr2 | 201768859 | |||||||
| chr2:201768963 | G | A | 1 | a0001c0001t0001g0038 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-60-18C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201768963 | |||||||
| chr2:201769002 | T | TA | 110 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(107): Show |
121 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.-60-58dupT | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201769002 | |||||||
| chr2:201769263 | G | A | 7 | a0003c0007t0001g0032 a0003c0007t0001g0033 a0003c0007t0001g0034 others(4): Show |
7 | HG01496.hp2 HG02258.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.-60-318C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201769263 | |||||||
| chr2:201769273 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-60-328G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201769273 | |||||||
| chr2:201769325 | A | G | 104 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(101): Show |
115 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.-60-380T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201769325 | |||||||
| chr2:201769613 | T | C | 6 | a0001c0003t0002g0011 a0001c0003t0002g0189 a0001c0003t0002g0190 others(3): Show |
7 | HG00544.hp1 HG02155.hp1 HG02165.hp1 others(4): Show |
intron_variant | MODIFIER | c.-60-668A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201769613 | |||||||
| chr2:201769661 | T | C | 1 | a0002c0005t0001g0068 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-60-716A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201769661 | |||||||
| chr2:201770095 | C | A | 6 | a0003c0007t0001g0032 a0003c0007t0001g0033 a0003c0007t0001g0034 others(3): Show |
6 | HG01496.hp2 HG02280.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-60-1150G>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201770095 | |||||||
| chr2:201770120 | G | T | 2 | a0001c0004t0001g0074 a0001c0004t0001g0075 |
2 | HG02293.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-60-1175C>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201770120 | |||||||
| chr2:201770309 | CCTA | C | 9 | a0001c0001t0001g0046 a0001c0004t0001g0004 a0001c0004t0001g0044 others(6): Show |
10 | HG00642.hp1 HG00738.hp2 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.-60-1367_-60-1365d others(5): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201770309 | |||||||
| chr2:201770450 | A | AT | 12 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0022 others(9): Show |
12 | HG01109.hp2 HG01123.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.-60-1506dupA | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201770450 | |||||||
| chr2:201770450 | AT | A | 238 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(235): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.-60-1506delA | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201770450 | |||||||
| chr2:201770466 | TA | T | 3 | a0001c0003t0001g0042 a0001c0003t0007g0040 a0001c0003t0007g0041 |
3 | HG02486.hp1 HG02622.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-60-1522delT | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201770466 | |||||||
| chr2:201770551 | G | C | 3 | a0001c0003t0002g0195 a0001c0003t0002g0196 a0001c0003t0002g0197 |
3 | NA18971.hp1 NA19004.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.-60-1606C>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201770551 | |||||||
| chr2:201770686 | G | A | 1 | a0001c0002t0001g0314 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-60-1741C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201770686 | |||||||
| chr2:201770881 | T | C | 104 | a0001c0001t0001g0081 a0001c0001t0001g0083 a0001c0001t0001g0149 others(101): Show |
106 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.-60-1936A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201770881 | |||||||
| chr2:201770926 | A | C | 105 | a0001c0001t0001g0081 a0001c0001t0001g0083 a0001c0001t0001g0149 others(102): Show |
107 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.-60-1981T>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201770926 | |||||||
| chr2:201771027 | C | T | 320 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(317): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.-60-2082G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201771027 | |||||||
| chr2:201771042 | A | AT | 13 | a0001c0001t0001g0237 a0001c0001t0001g0242 a0001c0001t0001g0243 others(10): Show |
13 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(10): Show |
intron_variant | MODIFIER | c.-60-2098dupA | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201771042 | |||||||
| chr2:201771042 | AT | A | 66 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0222 others(63): Show |
71 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.-60-2098delA | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201771042 | |||||||
| chr2:201771042 | ATT | A | 151 | a0001c0001t0001g0038 a0001c0001t0001g0046 a0001c0001t0001g0081 others(148): Show |
158 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.-60-2099_-60-2098d others(4): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201771042 | |||||||
| chr2:201771042 | ATTT | A | 7 | a0001c0001t0003g0023 a0001c0001t0003g0031 a0003c0007t0001g0032 others(4): Show |
7 | HG01496.hp2 HG02055.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.-60-2100_-60-2098d others(5): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201771042 | |||||||
| chr2:201771116 | G | A | 6 | a0003c0007t0001g0032 a0003c0007t0001g0033 a0003c0007t0001g0034 others(3): Show |
6 | HG01496.hp2 HG02280.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-60-2171C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201771116 | |||||||
| chr2:201771203 | C | T | 1 | a0001c0004t0001g0157 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-60-2258G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201771203 | |||||||
| chr2:201771259 | C | T | 2 | a0003c0007t0001g0032 a0003c0007t0001g0033 |
2 | HG01496.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.-60-2314G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201771259 | |||||||
| chr2:201771298 | C | T | 2 | a0001c0003t0002g0088 a0008c0021t0001g0087 |
2 | HG00673.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.-60-2353G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201771298 | |||||||
| chr2:201771344 | A | T | 104 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(101): Show |
115 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.-60-2399T>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201771344 | |||||||
| chr2:201771348 | C | T | 104 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(101): Show |
115 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.-60-2403G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201771348 | |||||||
| chr2:201771414 | G | A | 60 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(57): Show |
65 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.-60-2469C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201771414 | |||||||
| chr2:201771429 | C | A | 104 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(101): Show |
115 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.-60-2484G>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201771429 | |||||||
| chr2:201771450 | T | C | 6 | a0003c0007t0001g0032 a0003c0007t0001g0033 a0003c0007t0001g0034 others(3): Show |
6 | HG01496.hp2 HG02280.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-60-2505A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201771450 | |||||||
| chr2:201771453 | T | C | 104 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(101): Show |
115 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.-60-2508A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201771453 | |||||||
| chr2:201771483 | T | C | 1 | a0001c0002t0001g0232 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-60-2538A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201771483 | |||||||
| chr2:201771693 | A | T | 4 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(1): Show |
4 | NA18967.hp2 NA18968.hp2 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.-60-2748T>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201771693 | |||||||
| chr2:201771722 | A | G | 104 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(101): Show |
115 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.-60-2777T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201771722 | |||||||
| chr2:201771921 | G | T | 1 | a0004c0008t0001g0236 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-60-2976C>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201771921 | |||||||
| chr2:201771929 | A | T | 2 | a0001c0003t0007g0040 a0001c0003t0007g0041 |
2 | HG02622.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-60-2984T>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201771929 | |||||||
| chr2:201772123 | G | A | 1 | a0001c0002t0001g0039 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-60-3178C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201772123 | |||||||
| chr2:201772188 | T | C | 87 | a0001c0001t0001g0149 a0001c0002t0001g0007 a0001c0002t0001g0008 others(84): Show |
89 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.-60-3243A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201772188 | |||||||
| chr2:201772278 | T | TAAC | 177 | a0001c0001t0001g0081 a0001c0001t0001g0083 a0001c0001t0001g0149 others(174): Show |
185 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.-60-3336_-60-3334d others(5): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201772278 | |||||||
| chr2:201772278 | TAAC | T | 12 | a0001c0001t0001g0217 a0001c0001t0003g0020 a0001c0001t0003g0021 others(9): Show |
12 | HG01109.hp2 HG01123.hp1 HG02027.hp2 others(9): Show |
intron_variant | MODIFIER | c.-60-3336_-60-3334d others(5): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201772278 | |||||||
| chr2:201772318 | C | T | 69 | a0001c0001t0001g0205 a0001c0001t0001g0207 a0001c0001t0001g0208 others(66): Show |
75 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.-60-3373G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201772318 | |||||||
| chr2:201772359 | C | T | 1 | a0001c0001t0001g0038 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-60-3414G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201772359 | |||||||
| chr2:201772499 | A | G | 1 | a0001c0001t0001g0038 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-60-3554T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201772499 | |||||||
| chr2:201772503 | C | T | 6 | a0003c0007t0001g0032 a0003c0007t0001g0033 a0003c0007t0001g0034 others(3): Show |
6 | HG01496.hp2 HG02280.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-60-3558G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201772503 | |||||||
| chr2:201772530 | T | C | 1 | a0001c0002t0001g0150 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-60-3585A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201772530 | |||||||
| chr2:201772649 | C | T | 1 | a0001c0001t0001g0222 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-60-3704G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201772649 | |||||||
| chr2:201772706 | G | T | 9 | a0001c0001t0001g0237 a0001c0001t0001g0238 a0001c0001t0001g0241 others(6): Show |
9 | HG00597.hp1 HG00673.hp1 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.-60-3761C>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201772706 | |||||||
| chr2:201772850 | A | AT | 95 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(92): Show |
104 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.-60-3906dupA | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201772850 | |||||||
| chr2:201772850 | A | ATT | 21 | a0001c0001t0001g0012 a0001c0001t0001g0208 a0001c0001t0001g0209 others(18): Show |
22 | HG00597.hp1 HG00673.hp1 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.-60-3907_-60-3906d others(4): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201772850 | |||||||
| chr2:201772850 | AT | A | 27 | a0001c0001t0001g0081 a0001c0001t0001g0083 a0001c0001t0001g0222 others(24): Show |
27 | HG00280.hp1 HG00423.hp2 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.-60-3906delA | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201772850 | |||||||
| chr2:201772850 | ATT | A | 81 | a0001c0001t0001g0149 a0001c0002t0001g0007 a0001c0002t0001g0008 others(78): Show |
83 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.-60-3907_-60-3906d others(4): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201772850 | |||||||
| chr2:201772850 | ATTT | A | 27 | a0001c0001t0001g0205 a0001c0001t0003g0031 a0001c0002t0001g0072 others(24): Show |
31 | HG00099.hp1 HG00642.hp2 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.-60-3908_-60-3906d others(5): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201772850 | |||||||
| chr2:201772872 | T | TTC | 6 | a0003c0007t0001g0032 a0003c0007t0001g0033 a0003c0007t0001g0036 others(3): Show |
6 | HG01496.hp2 HG02258.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-60-3928_-60-3927i others(4): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201772872 | |||||||
| chr2:201772901 | G | A | 104 | a0001c0001t0001g0081 a0001c0001t0001g0083 a0001c0001t0001g0149 others(101): Show |
106 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.-60-3956C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201772901 | |||||||
| chr2:201773008 | C | T | 3 | a0002c0006t0001g0057 a0002c0006t0001g0058 a0002c0006t0001g0059 |
3 | HG00099.hp1 HG01081.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.-60-4063G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201773008 | |||||||
| chr2:201773142 | G | A | 1 | a0001c0001t0001g0038 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-60-4197C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201773142 | |||||||
| chr2:201773151 | C | A | 1 | a0001c0002t0001g0153 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-60-4206G>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201773151 | |||||||
| chr2:201773166 | T | A | 2 | a0001c0001t0006g0330 a0001c0001t0006g0331 |
2 | HG03098.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-60-4221A>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201773166 | |||||||
| chr2:201773167 | T | G | 2 | a0001c0001t0006g0330 a0001c0001t0006g0331 |
2 | HG03098.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-60-4222A>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201773167 | |||||||
| chr2:201773179 | G | A | 1 | a0001c0001t0001g0038 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-60-4234C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201773179 | |||||||
| chr2:201773282 | C | T | 1 | a0003c0007t0001g0033 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-60-4337G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201773282 | |||||||
| chr2:201773341 | C | T | 1 | a0001c0003t0002g0160 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-60-4396G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201773341 | |||||||
| chr2:201773358 | G | A | 3 | a0001c0003t0004g0154 a0001c0003t0004g0155 a0001c0003t0004g0156 |
3 | HG00741.hp1 HG01099.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.-60-4413C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201773358 | |||||||
| chr2:201773449 | A | G | 2 | a0001c0001t0001g0217 a0001c0004t0001g0216 |
2 | HG02027.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.-60-4504T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201773449 | |||||||
| chr2:201773525 | C | T | 5 | a0001c0002t0001g0069 a0001c0002t0001g0070 a0001c0002t0001g0071 others(2): Show |
5 | NA18942.hp2 NA18968.hp1 NA19007.hp1 others(2): Show |
intron_variant | MODIFIER | c.-60-4580G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201773525 | |||||||
| chr2:201773620 | G | A | 1 | a0001c0004t0001g0157 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-60-4675C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201773620 | |||||||
| chr2:201773621 | C | T | 105 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(102): Show |
116 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.-60-4676G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201773621 | |||||||
| chr2:201773722 | T | C | 1 | a0001c0002t0001g0158 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-60-4777A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201773722 | |||||||
| chr2:201773773 | C | G | 1 | a0001c0003t0001g0042 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-60-4828G>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201773773 | |||||||
| chr2:201773804 | C | T | 15 | a0002c0005t0001g0002 a0002c0005t0001g0005 a0002c0005t0001g0056 others(12): Show |
18 | HG00099.hp1 HG01074.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.-60-4859G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201773804 | |||||||
| chr2:201773805 | G | A | 1 | a0001c0001t0001g0038 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-60-4860C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201773805 | |||||||
| chr2:201773832 | G | A | 1 | a0001c0001t0003g0031 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-60-4887C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201773832 | |||||||
| chr2:201774001 | A | G | 1 | a0003c0007t0001g0032 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-60-5056T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201774001 | |||||||
| chr2:201774004 | T | C | 1 | a0001c0001t0001g0234 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-60-5059A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201774004 | |||||||
| chr2:201774147 | T | C | 108 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(105): Show |
119 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.-60-5202A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201774147 | |||||||
| chr2:201774266 | G | A | 2 | a0001c0001t0001g0217 a0001c0004t0001g0216 |
2 | HG02027.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.-60-5321C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201774266 | |||||||
| chr2:201774318 | A | G | 2 | a0001c0001t0001g0217 a0001c0004t0001g0216 |
2 | HG02027.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.-60-5373T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201774318 | |||||||
| chr2:201774326 | G | A | 1 | a0001c0002t0001g0324 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.-60-5381C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201774326 | |||||||
| chr2:201774475 | A | G | 189 | a0001c0001t0001g0081 a0001c0001t0001g0083 a0001c0001t0001g0149 others(186): Show |
200 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.-60-5530T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201774475 | |||||||
| chr2:201774556 | G | A | 48 | a0001c0001t0001g0207 a0001c0003t0001g0172 a0001c0003t0002g0003 others(45): Show |
53 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.-60-5611C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201774556 | |||||||
| chr2:201774629 | CTACTCAA others(5): Show |
C | 1 | a0001c0001t0001g0325 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-60-5696_-60-5685d others(14): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201774629 | |||||||
| chr2:201774649 | TAA | T | 13 | a0001c0001t0001g0222 a0001c0001t0001g0227 a0001c0002t0001g0221 others(10): Show |
13 | HG00140.hp1 HG00423.hp2 HG01069.hp2 others(10): Show |
intron_variant | MODIFIER | c.-60-5706_-60-5705d others(4): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201774649 | |||||||
| chr2:201774797 | T | C | 1 | a0001c0001t0001g0207 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-60-5852A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201774797 | |||||||
| chr2:201774880 | T | G | 4 | a0001c0001t0001g0326 a0001c0001t0001g0327 a0001c0001t0001g0328 others(1): Show |
4 | NA18945.hp2 NA18971.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.-60-5935A>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201774880 | |||||||
| chr2:201775049 | G | C | 1 | a0001c0002t0001g0055 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-61+5828C>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201775049 | |||||||
| chr2:201775423 | A | G | 1 | a0004c0008t0001g0235 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-61+5454T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201775423 | |||||||
| chr2:201775532 | T | C | 1 | a0001c0002t0001g0202 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-61+5345A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201775532 | |||||||
| chr2:201775639 | T | C | 14 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0022 others(11): Show |
14 | HG01109.hp2 HG01123.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.-61+5238A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201775639 | |||||||
| chr2:201775718 | T | C | 1 | a0001c0002t0001g0052 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-61+5159A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201775718 | |||||||
| chr2:201775740 | C | A | 1 | a0001c0003t0002g0203 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-61+5137G>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201775740 | |||||||
| chr2:201775741 | C | A | 1 | a0001c0003t0002g0203 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-61+5136G>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201775741 | |||||||
| chr2:201775763 | T | C | 1 | a0001c0002t0001g0204 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-61+5114A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201775763 | |||||||
| chr2:201775792 | C | G | 1 | a0002c0005t0001g0056 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-61+5085G>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201775792 | |||||||
| chr2:201775823 | A | C | 1 | a0001c0001t0003g0031 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-61+5054T>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201775823 | |||||||
| chr2:201776039 | C | G | 1 | a0001c0002t0001g0055 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-61+4838G>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201776039 | |||||||
| chr2:201776171 | T | C | 1 | a0001c0001t0001g0205 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-61+4706A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201776171 | |||||||
| chr2:201776272 | T | C | 1 | a0001c0001t0001g0206 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-61+4605A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201776272 | |||||||
| chr2:201776374 | G | C | 1 | a0001c0001t0001g0207 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-61+4503C>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201776374 | |||||||
| chr2:201776534 | C | A | 7 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0210 others(4): Show |
7 | HG01243.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.-61+4343G>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201776534 | |||||||
| chr2:201776558 | T | C | 2 | a0001c0001t0001g0217 a0001c0004t0001g0216 |
2 | HG02027.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.-61+4319A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201776558 | |||||||
| chr2:201776720 | T | C | 2 | a0001c0001t0006g0330 a0001c0001t0006g0331 |
2 | HG03098.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-61+4157A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201776720 | |||||||
| chr2:201776795 | G | A | 1 | a0001c0002t0001g0215 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-61+4082C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201776795 | |||||||
| chr2:201777036 | T | C | 104 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(101): Show |
115 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.-61+3841A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201777036 | |||||||
| chr2:201777060 | C | G | 2 | a0001c0002t0001g0053 a0001c0002t0001g0054 |
2 | HG00280.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.-61+3817G>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201777060 | |||||||
| chr2:201777185 | C | T | 2 | a0001c0002t0001g0053 a0001c0002t0001g0054 |
2 | HG00280.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.-61+3692G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201777185 | |||||||
| chr2:201777261 | T | TAAAGAAA others(322): Show |
2 | a0001c0001t0003g0020 a0001c0001t0003g0021 |
2 | HG02895.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-61+3615_-61+3616i others(331): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201777261 | |||||||
| chr2:201777261 | T | TAAAGAAA others(323): Show |
5 | a0001c0001t0003g0022 a0001c0001t0003g0023 a0001c0001t0003g0024 others(2): Show |
5 | HG01109.hp2 HG01123.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.-61+3615_-61+3616i others(332): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201777261 | |||||||
| chr2:201777261 | T | TAAAGAAA others(324): Show |
1 | a0001c0001t0003g0027 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-61+3615_-61+3616i others(333): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201777261 | |||||||
| chr2:201777261 | T | TAAAGAAA others(325): Show |
2 | a0001c0001t0003g0030 a0001c0004t0003g0029 |
2 | HG02145.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-61+3615_-61+3616i others(334): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201777261 | |||||||
| chr2:201777261 | T | TAAAGAAA others(326): Show |
1 | a0001c0001t0003g0031 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-61+3615_-61+3616i others(335): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201777261 | |||||||
| chr2:201777261 | T | TAAAGAAA others(328): Show |
1 | a0001c0001t0006g0330 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-61+3615_-61+3616i others(337): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201777261 | |||||||
| chr2:201777261 | T | TAAAGAAA others(329): Show |
1 | a0001c0001t0006g0331 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-61+3615_-61+3616i others(338): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201777261 | |||||||
| chr2:201777261 | T | TAAAGAAA others(325): Show |
1 | a0001c0001t0003g0028 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-61+3615_-61+3616i others(334): Show |
ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201777261 | |||||||
| chr2:201777336 | G | A | 6 | a0003c0007t0001g0032 a0003c0007t0001g0033 a0003c0007t0001g0034 others(3): Show |
6 | HG01496.hp2 HG02280.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-61+3541C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201777336 | |||||||
| chr2:201777364 | G | A | 1 | a0001c0002t0001g0219 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-61+3513C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201777364 | |||||||
| chr2:201777491 | T | C | 1 | a0001c0003t0001g0042 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-61+3386A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201777491 | |||||||
| chr2:201777736 | T | C | 1 | a0001c0001t0001g0038 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-61+3141A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201777736 | |||||||
| chr2:201777963 | T | C | 2 | a0001c0001t0001g0217 a0001c0004t0001g0216 |
2 | HG02027.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.-61+2914A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201777963 | |||||||
| chr2:201778028 | T | C | 1 | a0015c0018t0001g0218 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-61+2849A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201778028 | |||||||
| chr2:201778386 | G | C | 2 | a0001c0001t0006g0330 a0001c0001t0006g0331 |
2 | HG03098.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-61+2491C>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201778386 | |||||||
| chr2:201778500 | C | A | 1 | a0001c0002t0001g0219 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-61+2377G>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201778500 | |||||||
| chr2:201778720 | G | A | 12 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0022 others(9): Show |
12 | HG01109.hp2 HG01123.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.-61+2157C>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201778720 | |||||||
| chr2:201779194 | G | C | 13 | a0001c0001t0001g0222 a0001c0001t0001g0227 a0001c0002t0001g0221 others(10): Show |
13 | HG00140.hp1 HG00423.hp2 HG01069.hp2 others(10): Show |
intron_variant | MODIFIER | c.-61+1683C>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201779194 | |||||||
| chr2:201779600 | C | T | 1 | a0001c0002t0001g0052 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-61+1277G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201779600 | |||||||
| chr2:201779832 | T | C | 1 | a0001c0002t0001g0233 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-61+1045A>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201779832 | |||||||
| chr2:201779942 | A | G | 9 | a0001c0001t0001g0046 a0001c0004t0001g0004 a0001c0004t0001g0044 others(6): Show |
10 | HG00642.hp1 HG00738.hp2 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.-61+935T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201779942 | |||||||
| chr2:201780215 | A | G | 3 | a0001c0003t0001g0042 a0001c0003t0007g0040 a0001c0003t0007g0041 |
3 | HG02486.hp1 HG02622.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-61+662T>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201780215 | |||||||
| chr2:201780490 | G | C | 1 | a0001c0001t0001g0234 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-61+387C>G | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201780490 | |||||||
| chr2:201780628 | C | A | 104 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(101): Show |
115 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.-61+249G>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201780628 | |||||||
| chr2:201780674 | C | A | 2 | a0001c0001t0006g0330 a0001c0001t0006g0331 |
2 | HG03098.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-61+203G>T | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201780674 | |||||||
| chr2:201780744 | C | T | 1 | a0001c0002t0001g0039 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-61+133G>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201780744 | |||||||
| chr2:201780781 | C | G | 1 | a0001c0001t0001g0038 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-61+96G>C | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201780781 | |||||||
| chr2:201780819 | G | T | 6 | a0003c0007t0001g0032 a0003c0007t0001g0033 a0003c0007t0001g0034 others(3): Show |
6 | HG01496.hp2 HG02280.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-61+58C>A | ALS2 | ENSG00000003393.16 | transcript | ENST00000264276.11 | protein_coding | 1/33 | chr2 | 201780819 |