Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 10847 |
| ensemblid | ENSG00000080603.17 |
| hgncid | 16974 |
| symbol | SRCAP |
| name | Snf2 related CREBBP activator protein |
| refseq_nuc | NM_006662.3 |
| refseq_prot | NP_006653.2 |
| ensembl_nuc | ENST00000262518.9 |
| ensembl_prot | ENSP00000262518.4 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 30699171 |
| end | 30741409 |
| strand | + |
| ver | v1.2 |
| region | chr16:30699171-30741409 |
| region5000 | chr16:30694171-30746409 |
| regionname0 | SRCAP_chr16_30699171_30741409 |
| regionname5000 | SRCAP_chr16_30694171_30746409 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 3230 | 185 | 60 | 49 | 47 | 12 | 15 | 32 | SRCAP_chr16_30694171_30746409 | SRCAP | MQSSP others(3225): Show |
chr16 | 30694171 | 30746409 |
| a0002 | 0/0 | 3230 | 5 | 0 | 5 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | MQSSP others(3225): Show |
chr16 | 30694171 | 30746409 |
| a0003 | 0/0 | 3230 | 3 | 1 | 0 | 0 | 2 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | MQSSP others(3225): Show |
chr16 | 30694171 | 30746409 |
| a0004 | 0/0 | 3230 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | MQSSP others(3225): Show |
chr16 | 30694171 | 30746409 |
| a0005 | 0/0 | 3230 | 2 | 0 | 0 | 1 | 0 | 1 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | MQSSP others(3225): Show |
chr16 | 30694171 | 30746409 |
| a0006 | 0/0 | 3230 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | SRCAP_chr16_30694171_30746409 | SRCAP | MQSSP others(3225): Show |
chr16 | 30694171 | 30746409 |
| a0007 | 0/0 | 3230 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | MQSSP others(3225): Show |
chr16 | 30694171 | 30746409 |
| a0008 | 0/0 | 3230 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | MQSSP others(3225): Show |
chr16 | 30694171 | 30746409 |
| a0009 | 0/0 | 3230 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | MQSSP others(3225): Show |
chr16 | 30694171 | 30746409 |
| a0010 | 0/0 | 3230 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | MQSSP others(3225): Show |
chr16 | 30694171 | 30746409 |
| a0011 | 0/0 | 3230 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SRCAP_chr16_30694171_30746409 | SRCAP | MQSSP others(3225): Show |
chr16 | 30694171 | 30746409 |
| a0012 | 0/0 | 3230 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SRCAP_chr16_30694171_30746409 | SRCAP | MQSSP others(3225): Show |
chr16 | 30694171 | 30746409 |
| a0013 | 0/0 | 3230 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | MQSSP others(3225): Show |
chr16 | 30694171 | 30746409 |
| a0014 | 0/0 | 3230 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SRCAP_chr16_30694171_30746409 | SRCAP | MQSSP others(3225): Show |
chr16 | 30694171 | 30746409 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 9690 | 157 | 38 | 46 | 46 | 12 | 14 | SRCAP_chr16_30694171_30746409 | SRCAP | ATGCA others(9685): Show |
chr16 | 30694171 | 30746409 | ||
| a0001c0002 | 1/0 | 9690 | 7 | 5 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | ATGCA others(9685): Show |
chr16 | 30694171 | 30746409 | ||
| a0001c0003 | 0/0 | 9690 | 7 | 6 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | ATGCA others(9685): Show |
chr16 | 30694171 | 30746409 | ||
| a0001c0005 | 0/0 | 9690 | 4 | 4 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | ATGCA others(9685): Show |
chr16 | 30694171 | 30746409 | ||
| a0001c0007 | 0/0 | 9690 | 3 | 3 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | ATGCA others(9685): Show |
chr16 | 30694171 | 30746409 | ||
| a0001c0011 | 0/0 | 9690 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | ATGCA others(9685): Show |
chr16 | 30694171 | 30746409 | ||
| a0001c0014 | 0/0 | 9690 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | ATGCA others(9685): Show |
chr16 | 30694171 | 30746409 | ||
| a0001c0015 | 0/0 | 9690 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | ATGCA others(9685): Show |
chr16 | 30694171 | 30746409 | ||
| a0001c0016 | 0/0 | 9690 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | ATGCA others(9685): Show |
chr16 | 30694171 | 30746409 | ||
| a0001c0020 | 0/0 | 9690 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | ATGCA others(9685): Show |
chr16 | 30694171 | 30746409 | ||
| a0001c0024 | 0/0 | 9690 | 1 | 0 | 0 | 0 | 0 | 1 | SRCAP_chr16_30694171_30746409 | SRCAP | ATGCA others(9685): Show |
chr16 | 30694171 | 30746409 | ||
| a0001c0025 | 0/0 | 9690 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | ATGCA others(9685): Show |
chr16 | 30694171 | 30746409 | ||
| a0002c0004 | 0/0 | 9690 | 4 | 0 | 4 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | ATGCA others(9685): Show |
chr16 | 30694171 | 30746409 | ||
| a0002c0013 | 0/0 | 9690 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | ATGCA others(9685): Show |
chr16 | 30694171 | 30746409 | ||
| a0003c0008 | 0/0 | 9690 | 3 | 1 | 0 | 0 | 2 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | ATGCA others(9685): Show |
chr16 | 30694171 | 30746409 | ||
| a0004c0006 | 0/0 | 9690 | 3 | 3 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | ATGCA others(9685): Show |
chr16 | 30694171 | 30746409 | ||
| a0005c0009 | 0/0 | 9690 | 2 | 0 | 0 | 1 | 0 | 1 | SRCAP_chr16_30694171_30746409 | SRCAP | ATGCA others(9685): Show |
chr16 | 30694171 | 30746409 | ||
| a0006c0010 | 0/0 | 9690 | 2 | 0 | 0 | 2 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | ATGCA others(9685): Show |
chr16 | 30694171 | 30746409 | ||
| a0007c0012 | 0/0 | 9690 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | ATGCA others(9685): Show |
chr16 | 30694171 | 30746409 | ||
| a0008c0021 | 0/0 | 9690 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | ATGCA others(9685): Show |
chr16 | 30694171 | 30746409 | ||
| a0009c0022 | 0/0 | 9690 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | ATGCA others(9685): Show |
chr16 | 30694171 | 30746409 | ||
| a0010c0023 | 0/0 | 9690 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | ATGCA others(9685): Show |
chr16 | 30694171 | 30746409 | ||
| a0011c0026 | 0/0 | 9690 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | ATGCA others(9685): Show |
chr16 | 30694171 | 30746409 | ||
| a0012c0019 | 0/0 | 9690 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | ATGCA others(9685): Show |
chr16 | 30694171 | 30746409 | ||
| a0013c0018 | 0/0 | 9690 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | ATGCA others(9685): Show |
chr16 | 30694171 | 30746409 | ||
| a0014c0017 | 0/0 | 9690 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | ATGCA others(9685): Show |
chr16 | 30694171 | 30746409 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 11723 | 80 | 30 | 14 | 22 | 6 | 8 | SRCAP_chr16_30694171_30746409 | SRCAP | GTCAG others(11718): Show |
chr16 | 30694171 | 30746409 |
| a0001c0001t0002 | 0/1 | 11724 | 65 | 0 | 31 | 23 | 4 | 6 | SRCAP_chr16_30694171_30746409 | SRCAP | GTCAG others(11719): Show |
chr16 | 30694171 | 30746409 |
| a0001c0001t0004 | 0/0 | 11722 | 4 | 3 | 0 | 0 | 1 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | GTCAG others(11717): Show |
chr16 | 30694171 | 30746409 |
| a0001c0001t0005 | 0/0 | 11723 | 5 | 5 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | GTCAG others(11718): Show |
chr16 | 30694171 | 30746409 |
| a0001c0001t0007 | 0/0 | 11724 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | GTCAG others(11719): Show |
chr16 | 30694171 | 30746409 |
| a0001c0001t0009 | 0/0 | 11724 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | GTCAG others(11719): Show |
chr16 | 30694171 | 30746409 |
| a0001c0001t0010 | 0/0 | 11724 | 1 | 0 | 0 | 0 | 1 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | GTCAG others(11719): Show |
chr16 | 30694171 | 30746409 |
| a0001c0002t0003 | 1/0 | 11724 | 7 | 5 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | GTCAG others(11719): Show |
chr16 | 30694171 | 30746409 |
| a0001c0003t0002 | 0/0 | 11724 | 7 | 6 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | GTCAG others(11719): Show |
chr16 | 30694171 | 30746409 |
| a0001c0005t0001 | 0/0 | 11723 | 4 | 4 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | GTCAG others(11718): Show |
chr16 | 30694171 | 30746409 |
| a0001c0007t0006 | 0/0 | 11724 | 3 | 3 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | GTCAG others(11719): Show |
chr16 | 30694171 | 30746409 |
| a0001c0011t0001 | 0/0 | 11723 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | GTCAG others(11718): Show |
chr16 | 30694171 | 30746409 |
| a0001c0014t0001 | 0/0 | 11723 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | GTCAG others(11718): Show |
chr16 | 30694171 | 30746409 |
| a0001c0015t0002 | 0/0 | 11724 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | GTCAG others(11719): Show |
chr16 | 30694171 | 30746409 |
| a0001c0016t0001 | 0/0 | 11723 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | GTCAG others(11718): Show |
chr16 | 30694171 | 30746409 |
| a0001c0020t0002 | 0/0 | 11724 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | GTCAG others(11719): Show |
chr16 | 30694171 | 30746409 |
| a0001c0024t0001 | 0/0 | 11723 | 1 | 0 | 0 | 0 | 0 | 1 | SRCAP_chr16_30694171_30746409 | SRCAP | GTCAG others(11718): Show |
chr16 | 30694171 | 30746409 |
| a0001c0025t0002 | 0/0 | 11724 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | GTCAG others(11719): Show |
chr16 | 30694171 | 30746409 |
| a0002c0004t0001 | 0/0 | 11723 | 3 | 0 | 3 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | GTCAG others(11718): Show |
chr16 | 30694171 | 30746409 |
| a0002c0004t0004 | 0/0 | 11722 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | GTCAG others(11717): Show |
chr16 | 30694171 | 30746409 |
| a0002c0013t0001 | 0/0 | 11723 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | GTCAG others(11718): Show |
chr16 | 30694171 | 30746409 |
| a0003c0008t0002 | 0/0 | 11724 | 3 | 1 | 0 | 0 | 2 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | GTCAG others(11719): Show |
chr16 | 30694171 | 30746409 |
| a0004c0006t0003 | 0/0 | 11724 | 2 | 2 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | GTCAG others(11719): Show |
chr16 | 30694171 | 30746409 |
| a0004c0006t0008 | 0/0 | 11724 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | GTCAG others(11719): Show |
chr16 | 30694171 | 30746409 |
| a0005c0009t0001 | 0/0 | 11723 | 2 | 0 | 0 | 1 | 0 | 1 | SRCAP_chr16_30694171_30746409 | SRCAP | GTCAG others(11718): Show |
chr16 | 30694171 | 30746409 |
| a0006c0010t0001 | 0/0 | 11723 | 2 | 0 | 0 | 2 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | GTCAG others(11718): Show |
chr16 | 30694171 | 30746409 |
| a0007c0012t0003 | 0/0 | 11724 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | GTCAG others(11719): Show |
chr16 | 30694171 | 30746409 |
| a0008c0021t0002 | 0/0 | 11724 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | GTCAG others(11719): Show |
chr16 | 30694171 | 30746409 |
| a0009c0022t0002 | 0/0 | 11724 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | GTCAG others(11719): Show |
chr16 | 30694171 | 30746409 |
| a0010c0023t0002 | 0/0 | 11724 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | GTCAG others(11719): Show |
chr16 | 30694171 | 30746409 |
| a0011c0026t0001 | 0/0 | 11723 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | GTCAG others(11718): Show |
chr16 | 30694171 | 30746409 |
| a0012c0019t0001 | 0/0 | 11723 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | GTCAG others(11718): Show |
chr16 | 30694171 | 30746409 |
| a0013c0018t0001 | 0/0 | 11723 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | GTCAG others(11718): Show |
chr16 | 30694171 | 30746409 |
| a0014c0017t0001 | 0/0 | 11723 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | GTCAG others(11718): Show |
chr16 | 30694171 | 30746409 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0001g0002 | 0/0 | 6 | 0 | 0 | 4 | 0 | 2 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0001g0003 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0001g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0001g0016 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0002g0001 | 0/0 | 11 | 0 | 7 | 3 | 0 | 1 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0002g0005 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0002g0006 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0002g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0002g0154 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0004g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0004g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0004g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0004g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0005g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0005g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0005g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0007g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0009g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0001t0010g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0002t0003g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0002t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0002t0003g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0002t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0002t0003g0055 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0003t0002g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0003t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0003t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0003t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0003t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0003t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0005t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0005t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0005t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0005t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0007t0006g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0007t0006g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0007t0006g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0011t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0014t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0015t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0016t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0020t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0024t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0001c0025t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0002c0004t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0002c0004t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0002c0004t0004g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0002c0013t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0003c0008t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0003c0008t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0003c0008t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0004c0006t0003g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0004c0006t0008g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0005c0009t0001g0002 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0006c0010t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0006c0010t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0007c0012t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0008c0021t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0009c0022t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0010c0023t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0011c0026t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0012c0019t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0013c0018t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| a0014c0017t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0069 | EUR | GBR | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG00099 | hp2 | a0001 | c0001 | t0004 | g0110 | EUR | GBR | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0059 | EUR | GBR | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | GBR | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0006 | EUR | FIN | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | FIN | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0100 | EUR | FIN | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0070 | EUR | FIN | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | CHS | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | CHS | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | CHS | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0058 | AMR | PUR | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0092 | AMR | PUR | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | CHS | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0071 | AMR | PUR | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0073 | AMR | PUR | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0089 | AMR | PUR | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0078 | AMR | PUR | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG01069 | hp1 | a0002 | c0004 | t0001 | g0002 | AMR | PUR | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG01071 | hp2 | a0002 | c0004 | t0004 | g0002 | AMR | PUR | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0041 | AMR | PUR | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0094 | AMR | PUR | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG01109 | hp2 | a0001 | c0002 | t0003 | g0030 | AMR | PUR | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0044 | AMR | PUR | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0045 | AMR | PUR | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0043 | AMR | PUR | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0081 | AMR | PUR | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG01192 | hp1 | a0002 | c0004 | t0001 | g0002 | AMR | PUR | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG01243 | hp2 | a0001 | c0025 | t0002 | g0046 | AMR | PUR | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0083 | AMR | CLM | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | CLM | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0090 | AMR | CLM | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0072 | AMR | CLM | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0047 | AMR | CLM | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0091 | AMR | CLM | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0050 | AMR | CLM | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | CLM | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG01496 | hp1 | a0001 | c0003 | t0002 | g0103 | AMR | CLM | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0068 | AMR | CLM | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG01516 | hp1 | a0003 | c0008 | t0002 | g0098 | EUR | IBS | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0084 | EUR | IBS | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG01517 | hp1 | a0003 | c0008 | t0002 | g0099 | EUR | IBS | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0066 | EUR | IBS | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG01884 | hp1 | a0007 | c0012 | t0003 | g0028 | AFR | ACB | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG01884 | hp2 | a0001 | c0003 | t0002 | g0153 | AFR | ACB | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG01891 | hp1 | a0001 | c0016 | t0001 | g0151 | AFR | ACB | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG01891 | hp2 | a0004 | c0006 | t0008 | g0029 | AFR | ACB | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG01943 | hp1 | a0002 | c0004 | t0001 | g0023 | AMR | PEL | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0054 | AMR | PEL | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG01952 | hp2 | a0001 | c0001 | t0007 | g0102 | AMR | PEL | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG01975 | hp2 | a0002 | c0013 | t0001 | g0155 | AMR | PEL | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG02040 | hp1 | a0001 | c0001 | t0009 | g0077 | EAS | KHV | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG02055 | hp1 | a0001 | c0005 | t0001 | g0136 | AFR | ACB | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | KHV | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | KHV | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG02132 | hp2 | a0005 | c0009 | t0001 | g0002 | EAS | KHV | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG02145 | hp1 | a0001 | c0003 | t0002 | g0104 | AFR | ACB | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG02145 | hp2 | a0008 | c0021 | t0002 | g0093 | AFR | ACB | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG02257 | hp2 | a0009 | c0022 | t0002 | g0079 | AFR | ACB | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG02280 | hp2 | a0001 | c0007 | t0006 | g0026 | AFR | ACB | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0085 | SAS | PJL | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0101 | SAS | PJL | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0087 | SAS | PJL | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG02738 | hp1 | a0001 | c0024 | t0001 | g0111 | SAS | PJL | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG02809 | hp1 | a0001 | c0002 | t0003 | g0004 | AFR | GWD | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG02818 | hp1 | a0001 | c0005 | t0001 | g0132 | AFR | GWD | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG02886 | hp1 | a0001 | c0007 | t0006 | g0024 | AFR | GWD | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG02886 | hp2 | a0001 | c0001 | t0005 | g0148 | AFR | GWD | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG02896 | hp1 | a0001 | c0003 | t0002 | g0105 | AFR | GWD | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0011 | AFR | GWD | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG02897 | hp1 | a0001 | c0001 | t0004 | g0013 | AFR | GWD | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | ESN | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | ESN | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG02965 | hp1 | a0001 | c0001 | t0004 | g0035 | AFR | ESN | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG02965 | hp2 | a0001 | c0002 | t0003 | g0027 | AFR | ESN | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | ESN | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG02970 | hp2 | a0001 | c0005 | t0001 | g0133 | AFR | ESN | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG03139 | hp1 | a0001 | c0001 | t0005 | g0010 | AFR | ESN | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG03139 | hp2 | a0001 | c0014 | t0001 | g0034 | AFR | ESN | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG03195 | hp2 | a0001 | c0001 | t0005 | g0010 | AFR | ESN | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG03209 | hp1 | a0001 | c0001 | t0005 | g0149 | AFR | MSL | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | MSL | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG03486 | hp2 | a0001 | c0007 | t0006 | g0025 | AFR | MSL | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ESN | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG03516 | hp2 | a0001 | c0002 | t0003 | g0031 | AFR | ESN | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG03540 | hp1 | a0003 | c0008 | t0002 | g0056 | AFR | GWD | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG03540 | hp2 | a0001 | c0003 | t0002 | g0015 | AFR | GWD | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | MSL | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG03579 | hp2 | a0001 | c0002 | t0003 | g0004 | AFR | MSL | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0088 | SAS | PJL | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | BEB | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0080 | SAS | BEB | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | YRI | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| NA18747 | hp1 | a0006 | c0010 | t0001 | g0118 | EAS | CHB | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| NA18747 | hp2 | a0010 | c0023 | t0002 | g0060 | EAS | CHB | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| NA18906 | hp1 | a0001 | c0002 | t0003 | g0004 | AFR | YRI | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| NA18906 | hp2 | a0001 | c0011 | t0001 | g0150 | AFR | YRI | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| NA18939 | hp1 | a0011 | c0026 | t0001 | g0051 | EAS | JPT | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| NA18980 | hp2 | a0012 | c0019 | t0001 | g0002 | EAS | JPT | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| NA18984 | hp2 | a0001 | c0015 | t0002 | g0032 | EAS | JPT | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| NA19030 | hp1 | a0001 | c0020 | t0002 | g0095 | AFR | LWK | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| NA19030 | hp2 | a0013 | c0018 | t0001 | g0019 | AFR | LWK | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| NA19043 | hp1 | a0001 | c0003 | t0002 | g0015 | AFR | LWK | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| NA19043 | hp2 | a0001 | c0001 | t0005 | g0010 | AFR | LWK | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| NA19063 | hp1 | a0006 | c0010 | t0001 | g0127 | EAS | JPT | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| NA19091 | hp1 | a0014 | c0017 | t0001 | g0009 | EAS | JPT | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| NA19240 | hp1 | a0004 | c0006 | t0003 | g0012 | AFR | YRI | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | YRI | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0129 | EUR | TSI | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| NA20752 | hp2 | a0001 | c0001 | t0010 | g0140 | EUR | TSI | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | GIH | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| NA20905 | hp2 | a0005 | c0009 | t0001 | g0002 | SAS | GIH | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG06807 | hp1 | a0001 | c0005 | t0001 | g0134 | AFR | USA | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| NA20300 | hp1 | a0004 | c0006 | t0003 | g0012 | AFR | USA | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | USA | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | LWK | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| NA21309 | hp2 | a0001 | c0003 | t0002 | g0033 | AFR | LWK | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0154 | REF | REF | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0003 | g0055 | REF | REF | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:30704071 | C | T | 1 | a0011 | 1 | NA18939.hp1 | missense_variant | MODERATE | c.62C>T | p.Ser21Leu | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 4/34 | 417/11724 | 62/9693 | 21/3230 | chr16 | 30704071 | |||
| chr16:30711931 | A | G | 1 | a0010 | 1 | NA18747.hp2 | missense_variant | MODERATE | c.1589A>G | p.Glu530Gly | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 12/34 | 1944/11724 | 1589/9693 | 530/3230 | chr16 | 30711931 | |||
| chr16:30720328 | A | G | 1 | a0009 | 1 | HG02257.hp2 | missense_variant | MODERATE | c.2984A>G | p.Asn995Ser | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 19/34 | 3339/11724 | 2984/9693 | 995/3230 | chr16 | 30720328 | |||
| chr16:30720822 | T | C | 1 | a0002 | 5 | HG01069.hp1 HG01071.hp2 HG01192.hp1 others(2): Show |
missense_variant | MODERATE | c.3097T>C | p.Ser1033Pro | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 20/34 | 3452/11724 | 3097/9693 | 1033/3230 | chr16 | 30720822 | |||
| chr16:30720897 | C | T | 1 | a0005 | 2 | HG02132.hp2 NA20905.hp2 |
missense_variant | MODERATE | c.3172C>T | p.Pro1058Ser | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 20/34 | 3527/11724 | 3172/9693 | 1058/3230 | chr16 | 30720897 | |||
| chr16:30722256 | C | G | 1 | a0006 | 2 | NA18747.hp1 NA19063.hp1 |
missense_variant | MODERATE | c.3676C>G | p.Leu1226Val | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 22/34 | 4031/11724 | 3676/9693 | 1226/3230 | chr16 | 30722256 | |||
| chr16:30723613 | A | G | 1 | a0007 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.4189A>G | p.Ile1397Val | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 25/34 | 4544/11724 | 4189/9693 | 1397/3230 | chr16 | 30723613 | |||
| chr16:30724027 | C | G | 1 | a0003 | 3 | HG01516.hp1 HG01517.hp1 HG03540.hp1 |
missense_variant | MODERATE | c.4603C>G | p.Pro1535Ala | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 25/34 | 4958/11724 | 4603/9693 | 1535/3230 | chr16 | 30724027 | |||
| chr16:30724955 | C | G | 1 | a0008 | 1 | HG02145.hp2 | missense_variant | MODERATE | c.5531C>G | p.Ser1844Cys | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 25/34 | 5886/11724 | 5531/9693 | 1844/3230 | chr16 | 30724955 | |||
| chr16:30734539 | C | T | 1 | a0012 | 1 | NA18980.hp2 | missense_variant | MODERATE | c.6653C>T | p.Ser2218Phe | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 31/34 | 7008/11724 | 6653/9693 | 2218/3230 | chr16 | 30734539 | |||
| chr16:30737611 | C | G | 1 | a0013 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.7571C>G | p.Ser2524Cys | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 34/34 | 7926/11724 | 7571/9693 | 2524/3230 | chr16 | 30737611 | |||
| chr16:30738375 | C | T | 1 | a0014 | 1 | NA19091.hp1 | missense_variant | MODERATE | c.8335C>T | p.Pro2779Ser | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 34/34 | 8690/11724 | 8335/9693 | 2779/3230 | chr16 | 30738375 | |||
| chr16:30738390 | A | C | 1 | a0004 | 3 | HG01891.hp2 NA19240.hp1 NA20300.hp1 |
missense_variant | MODERATE | c.8350A>C | p.Thr2784Pro | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 34/34 | 8705/11724 | 8350/9693 | 2784/3230 | chr16 | 30738390 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:30704141 | C | T | 1 | a0001c0025 | 1 | HG01243.hp2 | synonymous_variant | LOW | c.132C>T | p.Gly44Gly | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 4/34 | 487/11724 | 132/9693 | 44/3230 | chr16 | 30704141 | |||
| chr16:30704198 | C | G | 1 | a0001c0003 | 7 | HG01496.hp1 HG01884.hp2 HG02145.hp1 others(4): Show |
synonymous_variant | LOW | c.189C>G | p.Pro63Pro | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 4/34 | 544/11724 | 189/9693 | 63/3230 | chr16 | 30704198 | |||
| chr16:30707194 | C | T | 1 | a0001c0024 | 1 | HG02738.hp1 | synonymous_variant | LOW | c.318C>T | p.Ile106Ile | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 5/34 | 673/11724 | 318/9693 | 106/3230 | chr16 | 30707194 | |||
| chr16:30712318 | T | C | 1 | a0001c0011 | 1 | NA18906.hp2 | synonymous_variant | LOW | c.1872T>C | p.Ile624Ile | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 13/34 | 2227/11724 | 1872/9693 | 624/3230 | chr16 | 30712318 | |||
| chr16:30712749 | G | T | 23 | a0001c0001 a0001c0003 a0001c0005 others(20): Show |
196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
synonymous_variant | LOW | c.2064G>T | p.Arg688Arg | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 14/34 | 2419/11724 | 2064/9693 | 688/3230 | chr16 | 30712749 | |||
| chr16:30713546 | T | C | 1 | a0005c0009 | 2 | HG02132.hp2 NA20905.hp2 |
synonymous_variant | LOW | c.2328T>C | p.Thr776Thr | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 16/34 | 2683/11724 | 2328/9693 | 776/3230 | chr16 | 30713546 | |||
| chr16:30722279 | G | A | 1 | a0001c0014 | 1 | HG03139.hp2 | synonymous_variant | LOW | c.3699G>A | p.Pro1233Pro | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 22/34 | 4054/11724 | 3699/9693 | 1233/3230 | chr16 | 30722279 | |||
| chr16:30723642 | C | A | 25 | a0001c0001 a0001c0003 a0001c0005 others(22): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
synonymous_variant | LOW | c.4218C>A | p.Ser1406Ser | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 25/34 | 4573/11724 | 4218/9693 | 1406/3230 | chr16 | 30723642 | |||
| chr16:30725055 | C | G | 2 | a0001c0020 a0008c0021 |
2 | HG02145.hp2 NA19030.hp1 |
synonymous_variant | LOW | c.5631C>G | p.Pro1877Pro | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 25/34 | 5986/11724 | 5631/9693 | 1877/3230 | chr16 | 30725055 | |||
| chr16:30736286 | T | C | 1 | a0001c0015 | 1 | NA18984.hp2 | synonymous_variant | LOW | c.6816T>C | p.Asn2272Asn | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 32/34 | 7171/11724 | 6816/9693 | 2272/3230 | chr16 | 30736286 | |||
| chr16:30736358 | C | T | 1 | a0002c0013 | 1 | HG01975.hp2 | synonymous_variant | LOW | c.6888C>T | p.Ser2296Ser | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 32/34 | 7243/11724 | 6888/9693 | 2296/3230 | chr16 | 30736358 | |||
| chr16:30737303 | C | A | 1 | a0001c0005 | 4 | HG02055.hp1 HG02818.hp1 HG02970.hp2 others(1): Show |
synonymous_variant | LOW | c.7263C>A | p.Arg2421Arg | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 34/34 | 7618/11724 | 7263/9693 | 2421/3230 | chr16 | 30737303 | |||
| chr16:30737579 | G | T | 1 | a0001c0007 | 3 | HG02280.hp2 HG02886.hp1 HG03486.hp2 |
synonymous_variant | LOW | c.7539G>T | p.Pro2513Pro | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 34/34 | 7894/11724 | 7539/9693 | 2513/3230 | chr16 | 30737579 | |||
| chr16:30739152 | T | C | 2 | a0001c0011 a0001c0016 |
2 | HG01891.hp1 NA18906.hp2 |
synonymous_variant | LOW | c.9112T>C | p.Leu3038Leu | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 34/34 | 9467/11724 | 9112/9693 | 3038/3230 | chr16 | 30739152 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:30700669 | C | T | 1 | a0001c0001t0010 | 1 | NA20752.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-156C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/34 | chr16 | 30700669 | |||||||
| chr16:30740075 | CT | C | 15 | a0001c0001t0001 a0001c0001t0005 a0001c0005t0001 others(12): Show |
105 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*358delT | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 34/34 | 358 | INFO_REALIGN_3_PRIME | chr16 | 30740075 | |||||
| chr16:30740075 | CTT | C | 2 | a0001c0001t0004 a0002c0004t0004 |
5 | HG00099.hp2 HG01071.hp2 HG02896.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*357_*358delTT | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 34/34 | 357 | INFO_REALIGN_3_PRIME | chr16 | 30740075 | |||||
| chr16:30740481 | G | A | 1 | a0001c0001t0007 | 1 | HG01952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*748G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 34/34 | 748 | chr16 | 30740481 | ||||||
| chr16:30740752 | C | T | 1 | a0001c0001t0009 | 1 | HG02040.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1019C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 34/34 | 1019 | chr16 | 30740752 | ||||||
| chr16:30740882 | A | G | 29 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(26): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
3_prime_UTR_variant | MODIFIER | c.*1149A>G | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 34/34 | 1149 | chr16 | 30740882 | ||||||
| chr16:30740913 | G | T | 1 | a0001c0001t0005 | 5 | HG02886.hp2 HG03139.hp1 HG03195.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1180G>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 34/34 | 1180 | chr16 | 30740913 | ||||||
| chr16:30740955 | A | G | 1 | a0001c0007t0006 | 3 | HG02280.hp2 HG02886.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1222A>G | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 34/34 | 1222 | chr16 | 30740955 | ||||||
| chr16:30741328 | A | G | 1 | a0004c0006t0008 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1595A>G | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 34/34 | 1595 | chr16 | 30741328 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:30699705 | T | A | 2 | a0001c0001t0002g0053 a0001c0001t0002g0065 |
2 | HG00673.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.-283-203T>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 1/33 | chr16 | 30699705 | |||||||
| chr16:30699736 | C | G | 1 | a0002c0013t0001g0155 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-283-172C>G | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 1/33 | chr16 | 30699736 | |||||||
| chr16:30699758 | C | A | 1 | a0002c0004t0001g0023 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-283-150C>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 1/33 | chr16 | 30699758 | |||||||
| chr16:30700245 | T | C | 12 | a0001c0001t0001g0011 a0001c0001t0004g0011 a0001c0002t0003g0004 others(9): Show |
15 | HG01109.hp2 HG01884.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.-210+264T>C | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 2/33 | chr16 | 30700245 | |||||||
| chr16:30700451 | C | T | 1 | a0001c0003t0002g0153 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-209-165C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 2/33 | chr16 | 30700451 | |||||||
| chr16:30700467 | G | C | 5 | a0001c0001t0001g0011 a0001c0001t0004g0011 a0001c0007t0006g0024 others(2): Show |
5 | HG02280.hp2 HG02886.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.-209-149G>C | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 2/33 | chr16 | 30700467 | |||||||
| chr16:30700503 | C | T | 2 | a0001c0001t0001g0003 a0001c0001t0001g0152 |
6 | HG02109.hp2 HG02809.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.-209-113C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 2/33 | chr16 | 30700503 | |||||||
| chr16:30700587 | CT | C | 22 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0036 others(19): Show |
25 | HG01099.hp2 HG01109.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.-209-14delT | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr16 | 30700587 | ||||||
| chr16:30700925 | G | A | 1 | a0001c0001t0001g0040 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.54+47G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/33 | chr16 | 30700925 | |||||||
| chr16:30700951 | G | T | 7 | a0001c0002t0003g0004 a0001c0002t0003g0027 a0001c0002t0003g0030 others(4): Show |
10 | HG01109.hp2 HG01884.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.54+73G>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/33 | chr16 | 30700951 | |||||||
| chr16:30701000 | C | A | 7 | a0001c0002t0003g0004 a0001c0002t0003g0027 a0001c0002t0003g0030 others(4): Show |
10 | HG01109.hp2 HG01884.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.54+122C>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/33 | chr16 | 30701000 | |||||||
| chr16:30701084 | C | T | 8 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(5): Show |
10 | HG01891.hp1 HG02280.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.54+206C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/33 | chr16 | 30701084 | |||||||
| chr16:30701154 | A | C | 5 | a0001c0001t0001g0022 a0001c0001t0001g0141 a0001c0001t0001g0142 others(2): Show |
6 | HG01928.hp1 HG01934.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.54+276A>C | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/33 | chr16 | 30701154 | |||||||
| chr16:30701157 | C | A | 1 | a0001c0001t0002g0041 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.54+279C>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/33 | chr16 | 30701157 | |||||||
| chr16:30701354 | A | G | 1 | a0001c0001t0010g0140 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.54+476A>G | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/33 | chr16 | 30701354 | |||||||
| chr16:30701636 | C | CT | 4 | a0001c0001t0001g0021 a0001c0001t0001g0038 a0001c0001t0001g0039 others(1): Show |
5 | HG01081.hp1 HG01099.hp2 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.54+773dupT | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/33 | INFO_REALIGN_3_PRIME | chr16 | 30701636 | ||||||
| chr16:30701666 | T | TTCTG | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(91): Show |
122 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.54+790_54+791insTG others(2): Show |
SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/33 | INFO_REALIGN_3_PRIME | chr16 | 30701666 | ||||||
| chr16:30701686 | A | G | 2 | a0001c0011t0001g0150 a0001c0016t0001g0151 |
2 | HG01891.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.54+808A>G | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/33 | chr16 | 30701686 | |||||||
| chr16:30701827 | C | A | 5 | a0001c0003t0002g0015 a0001c0003t0002g0033 a0001c0003t0002g0103 others(2): Show |
6 | HG01496.hp1 HG02145.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.54+949C>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/33 | chr16 | 30701827 | |||||||
| chr16:30701924 | G | A | 1 | a0001c0001t0002g0042 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.54+1046G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/33 | chr16 | 30701924 | |||||||
| chr16:30701926 | C | T | 1 | a0001c0001t0007g0102 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.54+1048C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/33 | chr16 | 30701926 | |||||||
| chr16:30701952 | C | CT | 5 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0002t0003g0004 others(2): Show |
7 | HG01109.hp2 HG02809.hp1 HG03516.hp2 others(4): Show |
intron_variant | MODIFIER | c.54+1088dupT | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/33 | INFO_REALIGN_3_PRIME | chr16 | 30701952 | ||||||
| chr16:30701952 | C | CTTT | 3 | a0001c0001t0005g0010 a0001c0001t0005g0148 a0001c0001t0005g0149 |
5 | HG02886.hp2 HG03139.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.54+1086_54+1088dup others(3): Show |
SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/33 | INFO_REALIGN_3_PRIME | chr16 | 30701952 | ||||||
| chr16:30701952 | CT | C | 5 | a0001c0001t0001g0011 a0001c0001t0004g0011 a0001c0007t0006g0024 others(2): Show |
5 | HG02280.hp2 HG02886.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.54+1088delT | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/33 | INFO_REALIGN_3_PRIME | chr16 | 30701952 | ||||||
| chr16:30701979 | G | C | 7 | a0001c0002t0003g0004 a0001c0002t0003g0027 a0001c0002t0003g0030 others(4): Show |
10 | HG01109.hp2 HG01884.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.54+1101G>C | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/33 | chr16 | 30701979 | |||||||
| chr16:30702057 | A | G | 2 | a0004c0006t0003g0012 a0004c0006t0008g0029 |
3 | HG01891.hp2 NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.54+1179A>G | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/33 | chr16 | 30702057 | |||||||
| chr16:30702101 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.54+1223G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/33 | chr16 | 30702101 | |||||||
| chr16:30702111 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.54+1233G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/33 | chr16 | 30702111 | |||||||
| chr16:30702377 | C | T | 1 | a0004c0006t0008g0029 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.54+1499C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/33 | chr16 | 30702377 | |||||||
| chr16:30702568 | TCCCTCCC others(6): Show |
T | 1 | a0001c0001t0002g0101 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.55-1493_55-1481del others(13): Show |
SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/33 | INFO_REALIGN_3_PRIME | chr16 | 30702568 | ||||||
| chr16:30702571 | C | T | 8 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(5): Show |
10 | HG01891.hp1 HG02280.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.55-1493C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/33 | chr16 | 30702571 | |||||||
| chr16:30702575 | CTCCCTCC others(15): Show |
C | 3 | a0001c0001t0001g0040 a0001c0001t0001g0138 a0012c0019t0001g0002 |
3 | NA18939.hp2 NA18965.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.55-1475_55-1454del others(22): Show |
SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/33 | INFO_REALIGN_3_PRIME | chr16 | 30702575 | ||||||
| chr16:30702602 | T | C | 4 | a0001c0002t0003g0004 a0001c0002t0003g0027 a0001c0002t0003g0030 others(1): Show |
6 | HG01109.hp2 HG02809.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.55-1462T>C | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/33 | chr16 | 30702602 | |||||||
| chr16:30702702 | G | A | 8 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0036 others(5): Show |
10 | HG02630.hp2 HG02895.hp1 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.55-1362G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/33 | chr16 | 30702702 | |||||||
| chr16:30702855 | C | T | 8 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(5): Show |
10 | HG01891.hp1 HG02280.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.55-1209C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/33 | chr16 | 30702855 | |||||||
| chr16:30702884 | T | A | 1 | a0007c0012t0003g0028 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.55-1180T>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/33 | chr16 | 30702884 | |||||||
| chr16:30703096 | T | C | 57 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(54): Show |
77 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.55-968T>C | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/33 | chr16 | 30703096 | |||||||
| chr16:30703149 | C | CTA | 15 | a0001c0001t0001g0018 a0001c0001t0001g0040 a0001c0001t0001g0131 others(12): Show |
19 | HG01168.hp1 HG01169.hp1 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.55-897_55-896dupAT | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/33 | INFO_REALIGN_3_PRIME | chr16 | 30703149 | ||||||
| chr16:30703149 | C | CTATA | 3 | a0001c0001t0001g0108 a0001c0003t0002g0103 a0001c0003t0002g0104 |
3 | HG01496.hp1 HG02145.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.55-899_55-896dupAT others(2): Show |
SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/33 | INFO_REALIGN_3_PRIME | chr16 | 30703149 | ||||||
| chr16:30703149 | C | CTATATAT others(3): Show |
4 | a0001c0002t0003g0004 a0001c0002t0003g0027 a0004c0006t0003g0012 others(1): Show |
7 | HG01891.hp2 HG02809.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.55-905_55-896dupAT others(8): Show |
SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/33 | INFO_REALIGN_3_PRIME | chr16 | 30703149 | ||||||
| chr16:30703149 | C | CTATATAT others(5): Show |
3 | a0001c0001t0001g0011 a0001c0001t0004g0011 a0001c0002t0003g0031 |
3 | HG02896.hp2 HG02897.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.55-907_55-896dupAT others(10): Show |
SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/33 | INFO_REALIGN_3_PRIME | chr16 | 30703149 | ||||||
| chr16:30703149 | C | CTATATAT others(7): Show |
4 | a0001c0002t0003g0030 a0001c0007t0006g0025 a0001c0007t0006g0026 others(1): Show |
4 | HG01109.hp2 HG01884.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.55-909_55-896dupAT others(12): Show |
SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/33 | INFO_REALIGN_3_PRIME | chr16 | 30703149 | ||||||
| chr16:30703149 | C | CTATATAT others(9): Show |
1 | a0001c0007t0006g0024 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.55-911_55-896dupAT others(14): Show |
SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/33 | INFO_REALIGN_3_PRIME | chr16 | 30703149 | ||||||
| chr16:30703172 | T | C | 1 | a0001c0001t0002g0047 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.55-892T>C | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/33 | chr16 | 30703172 | |||||||
| chr16:30703460 | C | G | 1 | a0001c0001t0001g0130 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.55-604C>G | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/33 | chr16 | 30703460 | |||||||
| chr16:30703505 | A | T | 2 | a0001c0001t0001g0020 a0001c0001t0001g0137 |
3 | HG01106.hp2 HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.55-559A>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/33 | chr16 | 30703505 | |||||||
| chr16:30703507 | A | T | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(91): Show |
122 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.55-557A>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/33 | chr16 | 30703507 | |||||||
| chr16:30703896 | CA | C | 76 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(73): Show |
100 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.55-161delA | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/33 | INFO_REALIGN_3_PRIME | chr16 | 30703896 | ||||||
| chr16:30703955 | A | C | 7 | a0001c0002t0003g0004 a0001c0002t0003g0027 a0001c0002t0003g0030 others(4): Show |
10 | HG01109.hp2 HG01884.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.55-109A>C | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/33 | chr16 | 30703955 | |||||||
| chr16:30704319 | C | T | 4 | a0001c0002t0003g0004 a0001c0002t0003g0027 a0001c0002t0003g0030 others(1): Show |
6 | HG01109.hp2 HG02809.hp1 HG02965.hp2 others(3): Show |
splice_region_variant&intron_variant | LOW | c.306+4C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 4/33 | chr16 | 30704319 | |||||||
| chr16:30704344 | C | T | 1 | a0001c0001t0010g0140 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.306+29C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 4/33 | chr16 | 30704344 | |||||||
| chr16:30704510 | A | G | 1 | a0001c0001t0001g0129 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.306+195A>G | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 4/33 | chr16 | 30704510 | |||||||
| chr16:30704587 | T | C | 95 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(92): Show |
123 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.306+272T>C | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 4/33 | chr16 | 30704587 | |||||||
| chr16:30704610 | G | C | 1 | a0001c0001t0010g0140 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.306+295G>C | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 4/33 | chr16 | 30704610 | |||||||
| chr16:30704649 | G | A | 1 | a0001c0005t0001g0132 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.306+334G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 4/33 | chr16 | 30704649 | |||||||
| chr16:30704739 | G | T | 1 | a0007c0012t0003g0028 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.306+424G>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 4/33 | chr16 | 30704739 | |||||||
| chr16:30704745 | G | A | 1 | a0001c0001t0001g0141 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.306+430G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 4/33 | chr16 | 30704745 | |||||||
| chr16:30705236 | G | A | 1 | a0001c0001t0001g0049 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.306+921G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 4/33 | chr16 | 30705236 | |||||||
| chr16:30705308 | G | T | 1 | a0001c0001t0001g0100 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.306+993G>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 4/33 | chr16 | 30705308 | |||||||
| chr16:30705318 | G | C | 1 | a0007c0012t0003g0028 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.306+1003G>C | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 4/33 | chr16 | 30705318 | |||||||
| chr16:30705429 | C | T | 2 | a0003c0008t0002g0098 a0003c0008t0002g0099 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.306+1114C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 4/33 | chr16 | 30705429 | |||||||
| chr16:30705548 | C | T | 2 | a0004c0006t0003g0012 a0004c0006t0008g0029 |
3 | HG01891.hp2 NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.306+1233C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 4/33 | chr16 | 30705548 | |||||||
| chr16:30705707 | G | GT | 12 | a0001c0001t0001g0097 a0001c0001t0002g0096 a0001c0001t0002g0144 others(9): Show |
15 | HG01109.hp2 HG01243.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.306+1405dupT | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 4/33 | INFO_REALIGN_3_PRIME | chr16 | 30705707 | ||||||
| chr16:30705765 | G | A | 6 | a0001c0002t0003g0004 a0001c0002t0003g0027 a0001c0002t0003g0030 others(3): Show |
9 | HG01109.hp2 HG01891.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.307-1418G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 4/33 | chr16 | 30705765 | |||||||
| chr16:30705854 | G | A | 1 | a0001c0014t0001g0034 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.307-1329G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 4/33 | chr16 | 30705854 | |||||||
| chr16:30706030 | T | G | 1 | a0001c0001t0002g0050 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.307-1153T>G | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 4/33 | chr16 | 30706030 | |||||||
| chr16:30706304 | A | G | 2 | a0001c0001t0001g0018 a0001c0001t0001g0131 |
3 | HG02109.hp1 HG02647.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.307-879A>G | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 4/33 | chr16 | 30706304 | |||||||
| chr16:30706465 | A | G | 6 | a0001c0003t0002g0015 a0001c0003t0002g0033 a0001c0003t0002g0103 others(3): Show |
7 | HG01496.hp1 HG01884.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.307-718A>G | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 4/33 | chr16 | 30706465 | |||||||
| chr16:30706536 | A | G | 1 | a0001c0001t0001g0106 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.307-647A>G | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 4/33 | chr16 | 30706536 | |||||||
| chr16:30706603 | G | A | 4 | a0001c0005t0001g0132 a0001c0005t0001g0133 a0001c0005t0001g0134 others(1): Show |
4 | HG02055.hp1 HG02818.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.307-580G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 4/33 | chr16 | 30706603 | |||||||
| chr16:30706609 | C | T | 2 | a0001c0007t0006g0024 a0001c0007t0006g0026 |
2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.307-574C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 4/33 | chr16 | 30706609 | |||||||
| chr16:30706637 | G | A | 2 | a0001c0001t0001g0011 a0001c0001t0004g0011 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.307-546G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 4/33 | chr16 | 30706637 | |||||||
| chr16:30706667 | C | A | 1 | a0011c0026t0001g0051 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.307-516C>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 4/33 | chr16 | 30706667 | |||||||
| chr16:30707176 | T | C | 1 | a0001c0001t0002g0052 | 1 | NA18980.hp1 | splice_region_variant&intron_variant | LOW | c.307-7T>C | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 4/33 | chr16 | 30707176 | |||||||
| chr16:30707439 | A | C | 1 | a0011c0026t0001g0051 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.492+71A>C | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 5/33 | chr16 | 30707439 | |||||||
| chr16:30707552 | C | T | 19 | a0001c0001t0001g0086 a0001c0001t0001g0100 a0001c0001t0002g0006 others(16): Show |
21 | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.493-20C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 5/33 | chr16 | 30707552 | |||||||
| chr16:30707721 | T | C | 1 | a0007c0012t0003g0028 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.633+9T>C | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 6/33 | chr16 | 30707721 | |||||||
| chr16:30707736 | G | A | 1 | a0004c0006t0008g0029 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.633+24G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 6/33 | chr16 | 30707736 | |||||||
| chr16:30707986 | C | T | 3 | a0001c0001t0002g0094 a0001c0020t0002g0095 a0008c0021t0002g0093 |
3 | HG01109.hp1 HG02145.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.633+274C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 6/33 | chr16 | 30707986 | |||||||
| chr16:30708077 | C | A | 4 | a0001c0005t0001g0132 a0001c0005t0001g0133 a0001c0005t0001g0134 others(1): Show |
4 | HG02055.hp1 HG02818.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.633+365C>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 6/33 | chr16 | 30708077 | |||||||
| chr16:30708503 | C | T | 3 | a0001c0003t0002g0015 a0001c0003t0002g0033 a0001c0003t0002g0104 |
4 | HG02145.hp1 HG03540.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.633+791C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 6/33 | chr16 | 30708503 | |||||||
| chr16:30708684 | G | A | 2 | a0001c0001t0001g0109 a0001c0001t0004g0110 |
2 | HG00099.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.634-829G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 6/33 | chr16 | 30708684 | |||||||
| chr16:30709055 | G | A | 1 | a0001c0001t0002g0053 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.634-458G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 6/33 | chr16 | 30709055 | |||||||
| chr16:30709279 | A | T | 1 | a0001c0001t0001g0017 | 2 | HG00438.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.634-234A>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 6/33 | chr16 | 30709279 | |||||||
| chr16:30709451 | G | A | 1 | a0001c0001t0002g0054 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.634-62G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 6/33 | chr16 | 30709451 | |||||||
| chr16:30710198 | G | C | 3 | a0001c0007t0006g0024 a0001c0007t0006g0025 a0001c0007t0006g0026 |
3 | HG02280.hp2 HG02886.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1134+70G>C | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 8/33 | chr16 | 30710198 | |||||||
| chr16:30710284 | T | C | 1 | a0001c0001t0001g0107 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1134+156T>C | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 8/33 | chr16 | 30710284 | |||||||
| chr16:30710965 | A | G | 1 | a0001c0001t0002g0092 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1229-34A>G | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 9/33 | chr16 | 30710965 | |||||||
| chr16:30711492 | G | A | 1 | a0001c0001t0002g0083 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1319-79G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 10/33 | chr16 | 30711492 | |||||||
| chr16:30711775 | G | A | 4 | a0001c0005t0001g0132 a0001c0005t0001g0133 a0001c0005t0001g0134 others(1): Show |
4 | HG02055.hp1 HG02818.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1492+31G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 11/33 | chr16 | 30711775 | |||||||
| chr16:30712605 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1994-74C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 13/33 | chr16 | 30712605 | |||||||
| chr16:30712900 | C | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.2130+85C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 14/33 | chr16 | 30712900 | |||||||
| chr16:30712901 | T | C | 2 | a0001c0001t0001g0011 a0001c0001t0004g0011 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2130+86T>C | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 14/33 | chr16 | 30712901 | |||||||
| chr16:30712920 | A | T | 1 | a0011c0026t0001g0051 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.2130+105A>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 14/33 | chr16 | 30712920 | |||||||
| chr16:30713075 | C | T | 1 | a0011c0026t0001g0051 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.2131-133C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 14/33 | chr16 | 30713075 | |||||||
| chr16:30713813 | G | T | 1 | a0006c0010t0001g0127 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2493+102G>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 16/33 | chr16 | 30713813 | |||||||
| chr16:30713831 | G | A | 8 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(5): Show |
10 | HG01891.hp1 HG02280.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.2493+120G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 16/33 | chr16 | 30713831 | |||||||
| chr16:30713900 | G | GT | 67 | a0001c0001t0001g0001 a0001c0001t0001g0049 a0001c0001t0001g0069 others(64): Show |
83 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.2493+204dupT | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 16/33 | INFO_REALIGN_3_PRIME | chr16 | 30713900 | ||||||
| chr16:30714034 | A | T | 4 | a0001c0001t0002g0050 a0001c0001t0002g0083 a0001c0001t0002g0090 others(1): Show |
4 | HG01255.hp1 HG01256.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.2493+323A>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 16/33 | chr16 | 30714034 | |||||||
| chr16:30714064 | A | AT | 17 | a0001c0001t0001g0040 a0001c0001t0001g0126 a0001c0001t0001g0135 others(14): Show |
18 | HG01109.hp2 HG01169.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.2493+372dupT | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 16/33 | INFO_REALIGN_3_PRIME | chr16 | 30714064 | ||||||
| chr16:30714133 | T | C | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(153): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.2493+422T>C | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 16/33 | chr16 | 30714133 | |||||||
| chr16:30714142 | G | A | 1 | a0003c0008t0002g0056 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2493+431G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 16/33 | chr16 | 30714142 | |||||||
| chr16:30714169 | A | G | 2 | a0001c0003t0002g0103 a0001c0003t0002g0105 |
2 | HG01496.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.2493+458A>G | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 16/33 | chr16 | 30714169 | |||||||
| chr16:30714399 | C | T | 3 | a0001c0001t0001g0009 a0001c0001t0001g0125 a0014c0017t0001g0009 |
4 | NA18945.hp1 NA19081.hp1 NA19088.hp2 others(1): Show |
intron_variant | MODIFIER | c.2493+688C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 16/33 | chr16 | 30714399 | |||||||
| chr16:30714460 | C | T | 1 | a0001c0001t0001g0139 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2493+749C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 16/33 | chr16 | 30714460 | |||||||
| chr16:30714498 | C | T | 2 | a0004c0006t0003g0012 a0004c0006t0008g0029 |
3 | HG01891.hp2 NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2493+787C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 16/33 | chr16 | 30714498 | |||||||
| chr16:30714507 | C | CTTTTTTT others(3): Show |
17 | a0001c0001t0001g0125 a0001c0001t0001g0145 a0001c0001t0001g0146 others(14): Show |
19 | HG01109.hp1 HG01168.hp1 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.2493+799_2493+808d others(12): Show |
SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 16/33 | INFO_REALIGN_3_PRIME | chr16 | 30714507 | ||||||
| chr16:30714507 | C | CTTTTTTT others(4): Show |
107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(104): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.2493+798_2493+808d others(13): Show |
SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 16/33 | INFO_REALIGN_3_PRIME | chr16 | 30714507 | ||||||
| chr16:30714507 | C | CTTTTTTT others(5): Show |
22 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0097 others(19): Show |
23 | HG00673.hp2 HG00738.hp1 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.2493+797_2493+808d others(14): Show |
SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 16/33 | INFO_REALIGN_3_PRIME | chr16 | 30714507 | ||||||
| chr16:30714507 | C | CTTTTTTT others(6): Show |
3 | a0001c0003t0002g0015 a0001c0003t0002g0104 a0008c0021t0002g0093 |
4 | HG02145.hp1 HG02145.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.2493+808_2493+809i others(15): Show |
SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 16/33 | INFO_REALIGN_3_PRIME | chr16 | 30714507 | ||||||
| chr16:30714507 | C | CTTTTTTT others(7): Show |
1 | a0001c0001t0001g0147 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2493+808_2493+809i others(16): Show |
SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 16/33 | INFO_REALIGN_3_PRIME | chr16 | 30714507 | ||||||
| chr16:30714593 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2493+882C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 16/33 | chr16 | 30714593 | |||||||
| chr16:30714655 | G | C | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(147): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.2493+944G>C | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 16/33 | chr16 | 30714655 | |||||||
| chr16:30714690 | C | T | 1 | a0001c0005t0001g0132 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2493+979C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 16/33 | chr16 | 30714690 | |||||||
| chr16:30714786 | T | C | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.2493+1075T>C | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 16/33 | chr16 | 30714786 | |||||||
| chr16:30714927 | C | T | 62 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(59): Show |
83 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.2494-1139C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 16/33 | chr16 | 30714927 | |||||||
| chr16:30714937 | T | G | 5 | a0001c0001t0001g0011 a0001c0001t0004g0011 a0001c0007t0006g0024 others(2): Show |
5 | HG02280.hp2 HG02886.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.2494-1129T>G | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 16/33 | chr16 | 30714937 | |||||||
| chr16:30715031 | CA | C | 3 | a0001c0007t0006g0024 a0001c0007t0006g0025 a0001c0007t0006g0026 |
3 | HG02280.hp2 HG02886.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2494-1034delA | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 16/33 | chr16 | 30715031 | |||||||
| chr16:30715214 | A | G | 1 | a0001c0001t0001g0119 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2494-852A>G | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 16/33 | chr16 | 30715214 | |||||||
| chr16:30715256 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2494-810G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 16/33 | chr16 | 30715256 | |||||||
| chr16:30715294 | G | A | 2 | a0001c0001t0001g0011 a0001c0001t0004g0011 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2494-772G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 16/33 | chr16 | 30715294 | |||||||
| chr16:30715579 | A | G | 4 | a0001c0005t0001g0132 a0001c0005t0001g0133 a0001c0005t0001g0134 others(1): Show |
4 | HG02055.hp1 HG02818.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.2494-487A>G | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 16/33 | chr16 | 30715579 | |||||||
| chr16:30715585 | A | G | 2 | a0001c0001t0002g0087 a0001c0001t0002g0088 |
2 | HG02735.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.2494-481A>G | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 16/33 | chr16 | 30715585 | |||||||
| chr16:30715646 | G | A | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(155): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.2494-420G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 16/33 | chr16 | 30715646 | |||||||
| chr16:30715722 | C | T | 1 | a0004c0006t0008g0029 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2494-344C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 16/33 | chr16 | 30715722 | |||||||
| chr16:30715906 | C | T | 1 | a0001c0003t0002g0153 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2494-160C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 16/33 | chr16 | 30715906 | |||||||
| chr16:30716532 | C | G | 2 | a0001c0001t0001g0049 a0001c0001t0002g0043 |
2 | HG01081.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.2817+53C>G | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 18/33 | chr16 | 30716532 | |||||||
| chr16:30716560 | T | G | 2 | a0001c0001t0001g0011 a0001c0001t0004g0011 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2817+81T>G | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 18/33 | chr16 | 30716560 | |||||||
| chr16:30716713 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2817+234C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 18/33 | chr16 | 30716713 | |||||||
| chr16:30717063 | C | T | 2 | a0001c0001t0001g0021 a0001c0001t0001g0039 |
3 | HG01081.hp1 HG01099.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.2817+584C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 18/33 | chr16 | 30717063 | |||||||
| chr16:30717103 | C | T | 1 | a0001c0001t0002g0041 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2817+624C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 18/33 | chr16 | 30717103 | |||||||
| chr16:30717123 | T | A | 1 | a0001c0007t0006g0025 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2817+644T>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 18/33 | chr16 | 30717123 | |||||||
| chr16:30717561 | C | T | 8 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(5): Show |
10 | HG01891.hp1 HG02280.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.2817+1082C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 18/33 | chr16 | 30717561 | |||||||
| chr16:30717610 | C | CT | 102 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(99): Show |
126 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.2817+1152dupT | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 18/33 | INFO_REALIGN_3_PRIME | chr16 | 30717610 | ||||||
| chr16:30717610 | C | CTT | 49 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0021 others(46): Show |
64 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(61): Show |
intron_variant | MODIFIER | c.2817+1151_2817+115 others(6): Show |
SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 18/33 | INFO_REALIGN_3_PRIME | chr16 | 30717610 | ||||||
| chr16:30717610 | C | CTTT | 4 | a0001c0001t0002g0005 a0001c0001t0002g0081 a0001c0001t0002g0082 others(1): Show |
6 | HG01175.hp1 HG01192.hp2 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.2817+1150_2817+115 others(7): Show |
SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 18/33 | INFO_REALIGN_3_PRIME | chr16 | 30717610 | ||||||
| chr16:30718302 | G | A | 5 | a0001c0001t0001g0011 a0001c0001t0004g0011 a0001c0007t0006g0024 others(2): Show |
5 | HG02280.hp2 HG02886.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.2817+1823G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 18/33 | chr16 | 30718302 | |||||||
| chr16:30718325 | C | T | 6 | a0001c0001t0001g0097 a0001c0001t0002g0014 a0001c0001t0002g0074 others(3): Show |
7 | HG02040.hp1 HG02129.hp2 NA18962.hp1 others(4): Show |
intron_variant | MODIFIER | c.2818-1837C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 18/33 | chr16 | 30718325 | |||||||
| chr16:30718418 | C | G | 2 | a0001c0001t0002g0072 a0001c0001t0002g0073 |
2 | HG00735.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.2818-1744C>G | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 18/33 | chr16 | 30718418 | |||||||
| chr16:30718475 | CT | C | 8 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(5): Show |
10 | HG01891.hp1 HG02280.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.2818-1671delT | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 18/33 | INFO_REALIGN_3_PRIME | chr16 | 30718475 | ||||||
| chr16:30718617 | G | A | 1 | a0001c0001t0002g0078 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2818-1545G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 18/33 | chr16 | 30718617 | |||||||
| chr16:30718953 | A | G | 78 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(75): Show |
102 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.2818-1209A>G | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 18/33 | chr16 | 30718953 | |||||||
| chr16:30718997 | A | T | 1 | a0001c0001t0001g0037 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2818-1165A>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 18/33 | chr16 | 30718997 | |||||||
| chr16:30718999 | C | T | 1 | a0001c0001t0001g0141 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.2818-1163C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 18/33 | chr16 | 30718999 | |||||||
| chr16:30719217 | T | TTTA | 67 | a0001c0001t0001g0001 a0001c0001t0001g0049 a0001c0001t0001g0069 others(64): Show |
83 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.2818-943_2818-942i others(5): Show |
SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 18/33 | INFO_REALIGN_3_PRIME | chr16 | 30719217 | ||||||
| chr16:30719222 | A | T | 67 | a0001c0001t0001g0001 a0001c0001t0001g0049 a0001c0001t0001g0069 others(64): Show |
83 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.2818-940A>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 18/33 | chr16 | 30719222 | |||||||
| chr16:30719222 | AT | A | 91 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(88): Show |
117 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.2818-929delT | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 18/33 | INFO_REALIGN_3_PRIME | chr16 | 30719222 | ||||||
| chr16:30719223 | T | A | 67 | a0001c0001t0001g0001 a0001c0001t0001g0049 a0001c0001t0001g0069 others(64): Show |
83 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.2818-939T>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 18/33 | chr16 | 30719223 | |||||||
| chr16:30719302 | G | A | 1 | a0001c0003t0002g0105 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2818-860G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 18/33 | chr16 | 30719302 | |||||||
| chr16:30719330 | T | C | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(155): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.2818-832T>C | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 18/33 | chr16 | 30719330 | |||||||
| chr16:30719358 | G | A | 62 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(59): Show |
83 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.2818-804G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 18/33 | chr16 | 30719358 | |||||||
| chr16:30719572 | G | A | 1 | a0010c0023t0002g0060 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2818-590G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 18/33 | chr16 | 30719572 | |||||||
| chr16:30719666 | A | G | 1 | a0001c0007t0006g0025 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2818-496A>G | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 18/33 | chr16 | 30719666 | |||||||
| chr16:30719870 | T | C | 1 | a0001c0001t0002g0054 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2818-292T>C | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 18/33 | chr16 | 30719870 | |||||||
| chr16:30719951 | G | C | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(147): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.2818-211G>C | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 18/33 | chr16 | 30719951 | |||||||
| chr16:30720518 | G | A | 1 | a0001c0001t0002g0061 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.2987+187G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 19/33 | chr16 | 30720518 | |||||||
| chr16:30721085 | C | G | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(155): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.3254-104C>G | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 20/33 | chr16 | 30721085 | |||||||
| chr16:30721564 | A | G | 2 | a0001c0001t0001g0013 a0001c0001t0004g0013 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3541+88A>G | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 21/33 | chr16 | 30721564 | |||||||
| chr16:30721591 | C | T | 1 | a0001c0001t0004g0110 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.3541+115C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 21/33 | chr16 | 30721591 | |||||||
| chr16:30721731 | T | G | 1 | a0001c0001t0002g0081 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.3541+255T>G | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 21/33 | chr16 | 30721731 | |||||||
| chr16:30722088 | G | T | 3 | a0001c0005t0001g0132 a0001c0005t0001g0134 a0001c0005t0001g0136 |
3 | HG02055.hp1 HG02818.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.3542-34G>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 21/33 | chr16 | 30722088 | |||||||
| chr16:30722783 | G | T | 1 | a0001c0001t0009g0077 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.3892+35G>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 23/33 | chr16 | 30722783 | |||||||
| chr16:30722864 | G | A | 1 | a0001c0001t0002g0062 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.3893-99G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 23/33 | chr16 | 30722864 | |||||||
| chr16:30723324 | A | G | 1 | a0001c0001t0001g0107 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.4159+95A>G | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 24/33 | chr16 | 30723324 | |||||||
| chr16:30723402 | T | C | 1 | a0001c0001t0002g0063 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.4159+173T>C | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 24/33 | chr16 | 30723402 | |||||||
| chr16:30725169 | A | C | 1 | a0001c0001t0001g0106 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.5658+87A>C | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 25/33 | chr16 | 30725169 | |||||||
| chr16:30725386 | T | G | 3 | a0001c0007t0006g0024 a0001c0007t0006g0025 a0001c0007t0006g0026 |
3 | HG02280.hp2 HG02886.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.5658+304T>G | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 25/33 | chr16 | 30725386 | |||||||
| chr16:30725421 | A | G | 6 | a0001c0003t0002g0015 a0001c0003t0002g0033 a0001c0003t0002g0103 others(3): Show |
7 | HG01496.hp1 HG01884.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.5658+339A>G | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 25/33 | chr16 | 30725421 | |||||||
| chr16:30725658 | T | C | 1 | a0001c0001t0002g0064 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.5658+576T>C | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 25/33 | chr16 | 30725658 | |||||||
| chr16:30725802 | T | A | 2 | a0001c0001t0001g0120 a0001c0024t0001g0111 |
2 | HG02738.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.5658+720T>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 25/33 | chr16 | 30725802 | |||||||
| chr16:30725993 | C | T | 1 | a0001c0001t0002g0059 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.5658+911C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 25/33 | chr16 | 30725993 | |||||||
| chr16:30726046 | T | G | 1 | a0001c0001t0002g0061 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.5658+964T>G | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 25/33 | chr16 | 30726046 | |||||||
| chr16:30726185 | T | C | 2 | a0001c0001t0002g0053 a0001c0001t0002g0065 |
2 | HG00673.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.5658+1103T>C | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 25/33 | chr16 | 30726185 | |||||||
| chr16:30726196 | C | T | 1 | a0001c0001t0002g0071 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.5658+1114C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 25/33 | chr16 | 30726196 | |||||||
| chr16:30726522 | CT | C | 5 | a0001c0001t0001g0135 a0001c0001t0002g0066 a0001c0001t0002g0090 others(2): Show |
5 | HG01256.hp1 HG01517.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.5658+1456delT | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 25/33 | INFO_REALIGN_3_PRIME | chr16 | 30726522 | ||||||
| chr16:30726584 | G | A | 19 | a0001c0001t0001g0086 a0001c0001t0001g0100 a0001c0001t0002g0006 others(16): Show |
21 | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.5658+1502G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 25/33 | chr16 | 30726584 | |||||||
| chr16:30726984 | G | A | 4 | a0001c0005t0001g0132 a0001c0005t0001g0133 a0001c0005t0001g0134 others(1): Show |
4 | HG02055.hp1 HG02818.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.5658+1902G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 25/33 | chr16 | 30726984 | |||||||
| chr16:30727140 | A | T | 1 | a0001c0001t0001g0117 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.5659-1826A>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 25/33 | chr16 | 30727140 | |||||||
| chr16:30727512 | A | G | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(153): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.5659-1454A>G | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 25/33 | chr16 | 30727512 | |||||||
| chr16:30727708 | C | T | 3 | a0001c0007t0006g0024 a0001c0007t0006g0025 a0001c0007t0006g0026 |
3 | HG02280.hp2 HG02886.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.5659-1258C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 25/33 | chr16 | 30727708 | |||||||
| chr16:30727844 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.5659-1122G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 25/33 | chr16 | 30727844 | |||||||
| chr16:30728170 | G | A | 3 | a0001c0007t0006g0024 a0001c0007t0006g0025 a0001c0007t0006g0026 |
3 | HG02280.hp2 HG02886.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.5659-796G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 25/33 | chr16 | 30728170 | |||||||
| chr16:30728598 | T | C | 62 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(59): Show |
83 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.5659-368T>C | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 25/33 | chr16 | 30728598 | |||||||
| chr16:30728610 | A | G | 1 | a0001c0001t0001g0112 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.5659-356A>G | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 25/33 | chr16 | 30728610 | |||||||
| chr16:30728743 | T | C | 1 | a0001c0001t0001g0117 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.5659-223T>C | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 25/33 | chr16 | 30728743 | |||||||
| chr16:30728821 | T | C | 152 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(149): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.5659-145T>C | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 25/33 | chr16 | 30728821 | |||||||
| chr16:30729737 | G | A | 4 | a0001c0005t0001g0132 a0001c0005t0001g0133 a0001c0005t0001g0134 others(1): Show |
4 | HG02055.hp1 HG02818.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.6127+165G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 27/33 | chr16 | 30729737 | |||||||
| chr16:30729918 | C | T | 2 | a0004c0006t0003g0012 a0004c0006t0008g0029 |
3 | HG01891.hp2 NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.6127+346C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 27/33 | chr16 | 30729918 | |||||||
| chr16:30730338 | C | CGCTTAAA others(14): Show |
155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.6127+766_6127+767i others(23): Show |
SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 27/33 | chr16 | 30730338 | |||||||
| chr16:30730353 | G | A | 1 | a0001c0003t0002g0103 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.6127+781G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 27/33 | chr16 | 30730353 | |||||||
| chr16:30730639 | T | C | 1 | a0001c0001t0001g0135 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.6127+1067T>C | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 27/33 | chr16 | 30730639 | |||||||
| chr16:30730642 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.6127+1070G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 27/33 | chr16 | 30730642 | |||||||
| chr16:30730729 | C | CT | 9 | a0001c0001t0001g0116 a0001c0001t0001g0145 a0001c0001t0001g0146 others(6): Show |
11 | HG01891.hp1 HG02280.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.6127+1171dupT | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 27/33 | INFO_REALIGN_3_PRIME | chr16 | 30730729 | ||||||
| chr16:30730928 | A | G | 1 | a0001c0001t0001g0139 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.6127+1356A>G | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 27/33 | chr16 | 30730928 | |||||||
| chr16:30730946 | A | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.6127+1374A>G | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 27/33 | chr16 | 30730946 | |||||||
| chr16:30731216 | T | C | 1 | a0001c0007t0006g0025 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.6127+1644T>C | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 27/33 | chr16 | 30731216 | |||||||
| chr16:30731453 | C | T | 3 | a0001c0007t0006g0024 a0001c0007t0006g0025 a0001c0007t0006g0026 |
3 | HG02280.hp2 HG02886.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.6128-1827C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 27/33 | chr16 | 30731453 | |||||||
| chr16:30731750 | C | T | 4 | a0001c0005t0001g0132 a0001c0005t0001g0133 a0001c0005t0001g0134 others(1): Show |
4 | HG02055.hp1 HG02818.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.6128-1530C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 27/33 | chr16 | 30731750 | |||||||
| chr16:30732201 | C | T | 68 | a0001c0001t0001g0001 a0001c0001t0001g0049 a0001c0001t0001g0069 others(65): Show |
84 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.6128-1079C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 27/33 | chr16 | 30732201 | |||||||
| chr16:30732236 | G | A | 2 | a0004c0006t0003g0012 a0004c0006t0008g0029 |
3 | HG01891.hp2 NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.6128-1044G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 27/33 | chr16 | 30732236 | |||||||
| chr16:30732392 | C | T | 3 | a0001c0007t0006g0024 a0001c0007t0006g0025 a0001c0007t0006g0026 |
3 | HG02280.hp2 HG02886.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.6128-888C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 27/33 | chr16 | 30732392 | |||||||
| chr16:30732705 | T | C | 3 | a0001c0007t0006g0024 a0001c0007t0006g0025 a0001c0007t0006g0026 |
3 | HG02280.hp2 HG02886.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.6128-575T>C | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 27/33 | chr16 | 30732705 | |||||||
| chr16:30732870 | T | G | 1 | a0001c0001t0010g0140 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.6128-410T>G | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 27/33 | chr16 | 30732870 | |||||||
| chr16:30732879 | C | T | 2 | a0001c0001t0002g0075 a0001c0001t0002g0076 |
2 | HG02129.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.6128-401C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 27/33 | chr16 | 30732879 | |||||||
| chr16:30732899 | C | A | 1 | a0001c0001t0002g0074 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.6128-381C>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 27/33 | chr16 | 30732899 | |||||||
| chr16:30733156 | T | C | 6 | a0001c0007t0006g0024 a0001c0007t0006g0025 a0001c0007t0006g0026 others(3): Show |
7 | HG01884.hp1 HG01891.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.6128-124T>C | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 27/33 | chr16 | 30733156 | |||||||
| chr16:30733505 | C | T | 4 | a0001c0001t0001g0070 a0001c0001t0002g0072 a0001c0001t0002g0073 others(1): Show |
4 | HG00323.hp2 HG00735.hp2 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.6297+56C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 28/33 | chr16 | 30733505 | |||||||
| chr16:30733516 | G | T | 1 | a0001c0003t0002g0104 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.6297+67G>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 28/33 | chr16 | 30733516 | |||||||
| chr16:30733886 | C | A | 2 | a0001c0001t0001g0011 a0001c0001t0004g0011 |
2 | HG02896.hp2 HG02897.hp2 |
splice_region_variant&intron_variant | LOW | c.6495-8C>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 29/33 | chr16 | 30733886 | |||||||
| chr16:30734141 | G | T | 2 | a0004c0006t0003g0012 a0004c0006t0008g0029 |
3 | HG01891.hp2 NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.6609+133G>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 30/33 | chr16 | 30734141 | |||||||
| chr16:30734215 | C | T | 1 | a0007c0012t0003g0028 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.6609+207C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 30/33 | chr16 | 30734215 | |||||||
| chr16:30734655 | C | T | 4 | a0001c0001t0001g0070 a0001c0001t0002g0072 a0001c0001t0002g0073 others(1): Show |
4 | HG00323.hp2 HG00735.hp2 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.6729+40C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 31/33 | chr16 | 30734655 | |||||||
| chr16:30734705 | A | G | 1 | a0001c0001t0001g0069 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.6729+90A>G | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 31/33 | chr16 | 30734705 | |||||||
| chr16:30734848 | T | C | 2 | a0001c0001t0002g0057 a0001c0015t0002g0032 |
2 | HG00438.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.6729+233T>C | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 31/33 | chr16 | 30734848 | |||||||
| chr16:30735136 | A | ATTTTTTT others(5): Show |
2 | a0001c0007t0006g0024 a0001c0007t0006g0026 |
2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.6729+538_6729+549d others(14): Show |
SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 31/33 | INFO_REALIGN_3_PRIME | chr16 | 30735136 | ||||||
| chr16:30735136 | A | ATTTTTTT others(7): Show |
1 | a0001c0007t0006g0025 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.6729+536_6729+549d others(16): Show |
SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 31/33 | INFO_REALIGN_3_PRIME | chr16 | 30735136 | ||||||
| chr16:30735136 | AT | A | 7 | a0001c0001t0001g0108 a0001c0003t0002g0015 a0001c0003t0002g0104 others(4): Show |
9 | HG01884.hp1 HG01891.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.6729+549delT | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 31/33 | INFO_REALIGN_3_PRIME | chr16 | 30735136 | ||||||
| chr16:30735136 | ATTTT | A | 6 | a0001c0001t0001g0119 a0001c0001t0001g0126 a0001c0001t0001g0138 others(3): Show |
6 | HG01175.hp2 HG01891.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.6729+546_6729+549d others(6): Show |
SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 31/33 | INFO_REALIGN_3_PRIME | chr16 | 30735136 | ||||||
| chr16:30735136 | ATTTTT | A | 67 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(64): Show |
89 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.6729+545_6729+549d others(7): Show |
SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 31/33 | INFO_REALIGN_3_PRIME | chr16 | 30735136 | ||||||
| chr16:30735136 | ATTTTTT | A | 4 | a0001c0001t0005g0010 a0001c0001t0005g0148 a0006c0010t0001g0118 others(1): Show |
6 | HG02886.hp2 HG03139.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.6729+544_6729+549d others(8): Show |
SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 31/33 | INFO_REALIGN_3_PRIME | chr16 | 30735136 | ||||||
| chr16:30735136 | ATTTTTTT others(3): Show |
A | 4 | a0001c0001t0001g0086 a0001c0001t0002g0063 a0001c0001t0002g0068 others(1): Show |
4 | HG00408.hp2 HG01496.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.6729+540_6729+549d others(12): Show |
SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 31/33 | INFO_REALIGN_3_PRIME | chr16 | 30735136 | ||||||
| chr16:30735136 | ATTTTTTT others(4): Show |
A | 61 | a0001c0001t0001g0001 a0001c0001t0001g0049 a0001c0001t0001g0069 others(58): Show |
77 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.6729+539_6729+549d others(13): Show |
SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 31/33 | INFO_REALIGN_3_PRIME | chr16 | 30735136 | ||||||
| chr16:30735136 | ATTTTTTT others(5): Show |
A | 3 | a0001c0001t0001g0097 a0001c0001t0002g0066 a0001c0001t0002g0082 |
3 | HG01517.hp2 NA18995.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.6729+538_6729+549d others(14): Show |
SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 31/33 | INFO_REALIGN_3_PRIME | chr16 | 30735136 | ||||||
| chr16:30735171 | G | A | 1 | a0001c0007t0006g0025 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.6729+556G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 31/33 | chr16 | 30735171 | |||||||
| chr16:30735177 | C | A | 1 | a0001c0001t0001g0152 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.6729+562C>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 31/33 | chr16 | 30735177 | |||||||
| chr16:30735240 | G | A | 2 | a0001c0011t0001g0150 a0001c0016t0001g0151 |
2 | HG01891.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.6729+625G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 31/33 | chr16 | 30735240 | |||||||
| chr16:30735357 | G | A | 2 | a0001c0007t0006g0024 a0001c0007t0006g0026 |
2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.6729+742G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 31/33 | chr16 | 30735357 | |||||||
| chr16:30735476 | C | T | 1 | a0001c0001t0001g0115 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.6730-724C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 31/33 | chr16 | 30735476 | |||||||
| chr16:30735501 | C | A | 78 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(75): Show |
102 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.6730-699C>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 31/33 | chr16 | 30735501 | |||||||
| chr16:30735567 | C | CT | 8 | a0001c0001t0001g0097 a0001c0001t0001g0100 a0001c0001t0002g0072 others(5): Show |
9 | HG00323.hp1 HG01256.hp2 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.6730-611dupT | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 31/33 | INFO_REALIGN_3_PRIME | chr16 | 30735567 | ||||||
| chr16:30735567 | C | CTT | 75 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0049 others(72): Show |
95 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.6730-612_6730-611d others(4): Show |
SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 31/33 | INFO_REALIGN_3_PRIME | chr16 | 30735567 | ||||||
| chr16:30735567 | C | CTTT | 66 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(63): Show |
87 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.6730-613_6730-611d others(5): Show |
SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 31/33 | INFO_REALIGN_3_PRIME | chr16 | 30735567 | ||||||
| chr16:30735567 | C | CTTTT | 5 | a0001c0001t0001g0039 a0001c0001t0001g0109 a0001c0001t0001g0114 others(2): Show |
5 | HG01099.hp2 HG01346.hp2 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.6730-614_6730-611d others(6): Show |
SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 31/33 | INFO_REALIGN_3_PRIME | chr16 | 30735567 | ||||||
| chr16:30735567 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.6730-633C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 31/33 | chr16 | 30735567 | |||||||
| chr16:30735567 | CTTTTTTT others(3): Show |
C | 2 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
2 | HG02280.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.6730-620_6730-611d others(12): Show |
SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 31/33 | INFO_REALIGN_3_PRIME | chr16 | 30735567 | ||||||
| chr16:30735605 | G | T | 1 | a0001c0001t0001g0135 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.6730-595G>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 31/33 | chr16 | 30735605 | |||||||
| chr16:30735631 | A | T | 1 | a0001c0001t0001g0135 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.6730-569A>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 31/33 | chr16 | 30735631 | |||||||
| chr16:30735649 | C | T | 3 | a0001c0007t0006g0024 a0001c0007t0006g0025 a0001c0007t0006g0026 |
3 | HG02280.hp2 HG02886.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.6730-551C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 31/33 | chr16 | 30735649 | |||||||
| chr16:30735826 | G | A | 4 | a0001c0001t0001g0113 a0001c0001t0001g0122 a0006c0010t0001g0118 others(1): Show |
4 | HG00673.hp2 NA18747.hp1 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.6730-374G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 31/33 | chr16 | 30735826 | |||||||
| chr16:30735870 | C | T | 78 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(75): Show |
102 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.6730-330C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 31/33 | chr16 | 30735870 | |||||||
| chr16:30736109 | C | T | 3 | a0001c0001t0001g0018 a0001c0001t0001g0131 a0001c0003t0002g0153 |
4 | HG01884.hp2 HG02109.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.6730-91C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 31/33 | chr16 | 30736109 | |||||||
| chr16:30736126 | T | C | 1 | a0001c0001t0002g0085 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.6730-74T>C | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 31/33 | chr16 | 30736126 | |||||||
| chr16:30736838 | A | C | 6 | a0001c0003t0002g0015 a0001c0003t0002g0033 a0001c0003t0002g0103 others(3): Show |
7 | HG01496.hp1 HG01884.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.7009-211A>C | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 33/33 | chr16 | 30736838 | |||||||
| chr16:30736862 | G | C | 3 | a0003c0008t0002g0056 a0003c0008t0002g0098 a0003c0008t0002g0099 |
3 | HG01516.hp1 HG01517.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.7009-187G>C | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 33/33 | chr16 | 30736862 | |||||||
| chr16:30737000 | T | C | 1 | a0001c0003t0002g0105 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.7009-49T>C | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 33/33 | chr16 | 30737000 |