Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 8831 |
| ensemblid | ENSG00000197283.18 |
| hgncid | 11497 |
| symbol | SYNGAP1 |
| name | synaptic Ras GTPase activating protein 1 |
| refseq_nuc | NM_006772.3 |
| refseq_prot | NP_006763.2 |
| ensembl_nuc | ENST00000646630.1 |
| ensembl_prot | ENSP00000496007.1 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 33420065 |
| end | 33453689 |
| strand | + |
| ver | v1.2 |
| region | chr6:33420065-33453689 |
| region5000 | chr6:33415065-33458689 |
| regionname0 | SYNGAP1_chr6_33420065_33453689 |
| regionname5000 | SYNGAP1_chr6_33415065_33458689 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 1343 | 296 | 89 | 62 | 99 | 15 | 30 | 61 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | MSRSR others(1338): Show |
chr6 | 33415065 | 33458689 |
| a0002 | 0/0 | 1343 | 9 | 0 | 1 | 7 | 1 | 0 | 7 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | MSRSR others(1338): Show |
chr6 | 33415065 | 33458689 |
| a0003 | 0/0 | 1343 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | MSRSR others(1338): Show |
chr6 | 33415065 | 33458689 |
| a0004 | 0/0 | 1343 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | MSRSR others(1338): Show |
chr6 | 33415065 | 33458689 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 4029 | 134 | 35 | 33 | 43 | 10 | 12 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | ATGAG others(4024): Show |
chr6 | 33415065 | 33458689 | ||
| a0001c0002 | 0/0 | 4029 | 102 | 23 | 20 | 44 | 2 | 13 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | ATGAG others(4024): Show |
chr6 | 33415065 | 33458689 | ||
| a0001c0003 | 0/0 | 4029 | 16 | 12 | 0 | 2 | 0 | 2 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | ATGAG others(4024): Show |
chr6 | 33415065 | 33458689 | ||
| a0001c0004 | 0/0 | 4029 | 14 | 14 | 0 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | ATGAG others(4024): Show |
chr6 | 33415065 | 33458689 | ||
| a0001c0005 | 0/0 | 4029 | 13 | 0 | 9 | 1 | 1 | 2 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | ATGAG others(4024): Show |
chr6 | 33415065 | 33458689 | ||
| a0001c0007 | 0/0 | 4029 | 6 | 4 | 0 | 2 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | ATGAG others(4024): Show |
chr6 | 33415065 | 33458689 | ||
| a0001c0008 | 0/0 | 4029 | 4 | 0 | 0 | 4 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | ATGAG others(4024): Show |
chr6 | 33415065 | 33458689 | ||
| a0001c0009 | 0/0 | 4029 | 2 | 0 | 0 | 0 | 2 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | ATGAG others(4024): Show |
chr6 | 33415065 | 33458689 | ||
| a0001c0010 | 0/0 | 4029 | 2 | 0 | 0 | 2 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | ATGAG others(4024): Show |
chr6 | 33415065 | 33458689 | ||
| a0001c0011 | 0/0 | 4029 | 2 | 0 | 0 | 1 | 0 | 1 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | ATGAG others(4024): Show |
chr6 | 33415065 | 33458689 | ||
| a0001c0013 | 0/0 | 4029 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | ATGAG others(4024): Show |
chr6 | 33415065 | 33458689 | ||
| a0002c0006 | 0/0 | 4029 | 9 | 0 | 1 | 7 | 1 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | ATGAG others(4024): Show |
chr6 | 33415065 | 33458689 | ||
| a0003c0012 | 0/0 | 4029 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | ATGAG others(4024): Show |
chr6 | 33415065 | 33458689 | ||
| a0004c0014 | 0/0 | 4029 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | ATGAG others(4024): Show |
chr6 | 33415065 | 33458689 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 6015 | 125 | 29 | 32 | 42 | 9 | 12 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | CTCTC others(6010): Show |
chr6 | 33415065 | 33458689 |
| a0001c0001t0002 | 0/0 | 6015 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | CTCTC others(6010): Show |
chr6 | 33415065 | 33458689 |
| a0001c0001t0003 | 0/0 | 6015 | 2 | 2 | 0 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | CTCTC others(6010): Show |
chr6 | 33415065 | 33458689 |
| a0001c0001t0004 | 0/0 | 6015 | 2 | 2 | 0 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | CTCTC others(6010): Show |
chr6 | 33415065 | 33458689 |
| a0001c0001t0006 | 0/0 | 6015 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | CTCTC others(6010): Show |
chr6 | 33415065 | 33458689 |
| a0001c0001t0008 | 0/0 | 6015 | 1 | 0 | 0 | 0 | 1 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | CTCTC others(6010): Show |
chr6 | 33415065 | 33458689 |
| a0001c0001t0010 | 0/0 | 6015 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | CTCTC others(6010): Show |
chr6 | 33415065 | 33458689 |
| a0001c0001t0014 | 0/0 | 6015 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | CTCTC others(6010): Show |
chr6 | 33415065 | 33458689 |
| a0001c0002t0001 | 0/0 | 6015 | 97 | 21 | 20 | 42 | 2 | 12 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | CTCTC others(6010): Show |
chr6 | 33415065 | 33458689 |
| a0001c0002t0002 | 0/0 | 6015 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | CTCTC others(6010): Show |
chr6 | 33415065 | 33458689 |
| a0001c0002t0005 | 0/0 | 6015 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | CTCCC others(6010): Show |
chr6 | 33415065 | 33458689 |
| a0001c0002t0007 | 0/0 | 6015 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | CTCTC others(6010): Show |
chr6 | 33415065 | 33458689 |
| a0001c0002t0009 | 0/0 | 6015 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | CTCTC others(6010): Show |
chr6 | 33415065 | 33458689 |
| a0001c0002t0013 | 0/0 | 6015 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | CTCTC others(6010): Show |
chr6 | 33415065 | 33458689 |
| a0001c0003t0001 | 0/0 | 6015 | 16 | 12 | 0 | 2 | 0 | 2 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | CTCTC others(6010): Show |
chr6 | 33415065 | 33458689 |
| a0001c0004t0001 | 0/0 | 6015 | 14 | 14 | 0 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | CTCTC others(6010): Show |
chr6 | 33415065 | 33458689 |
| a0001c0005t0001 | 0/0 | 6015 | 13 | 0 | 9 | 1 | 1 | 2 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | CTCTC others(6010): Show |
chr6 | 33415065 | 33458689 |
| a0001c0007t0001 | 0/0 | 6015 | 6 | 4 | 0 | 2 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | CTCTC others(6010): Show |
chr6 | 33415065 | 33458689 |
| a0001c0008t0001 | 0/0 | 6015 | 2 | 0 | 0 | 2 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | CTCTC others(6010): Show |
chr6 | 33415065 | 33458689 |
| a0001c0008t0011 | 0/0 | 6015 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | CTCTC others(6010): Show |
chr6 | 33415065 | 33458689 |
| a0001c0008t0012 | 0/0 | 6015 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | CTCTC others(6010): Show |
chr6 | 33415065 | 33458689 |
| a0001c0009t0001 | 0/0 | 6015 | 2 | 0 | 0 | 0 | 2 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | CTCTC others(6010): Show |
chr6 | 33415065 | 33458689 |
| a0001c0010t0001 | 0/0 | 6015 | 2 | 0 | 0 | 2 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | CTCTC others(6010): Show |
chr6 | 33415065 | 33458689 |
| a0001c0011t0001 | 0/0 | 6015 | 2 | 0 | 0 | 1 | 0 | 1 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | CTCTC others(6010): Show |
chr6 | 33415065 | 33458689 |
| a0001c0013t0001 | 0/0 | 6015 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | CTCTC others(6010): Show |
chr6 | 33415065 | 33458689 |
| a0002c0006t0001 | 0/0 | 6015 | 9 | 0 | 1 | 7 | 1 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | CTCTC others(6010): Show |
chr6 | 33415065 | 33458689 |
| a0003c0012t0001 | 0/0 | 6015 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | CTCTC others(6010): Show |
chr6 | 33415065 | 33458689 |
| a0004c0014t0001 | 0/0 | 6015 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | CTCTC others(6010): Show |
chr6 | 33415065 | 33458689 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0001t0001g0005 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0001t0001g0006 | 0/0 | 6 | 0 | 1 | 4 | 0 | 1 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0001t0001g0007 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0001t0001g0009 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0001t0001g0010 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0001t0001g0011 | 0/1 | 4 | 2 | 0 | 0 | 1 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0001t0001g0016 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0001t0001g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0001t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0001t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0001t0003g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0001t0004g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0001t0004g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0001t0006g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0001t0008g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0001t0010g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0001t0014g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0002t0001g0001 | 0/0 | 21 | 2 | 3 | 12 | 0 | 4 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0002t0001g0002 | 0/0 | 10 | 0 | 0 | 9 | 0 | 1 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0002t0001g0008 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0002t0001g0012 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0002t0001g0013 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0002t0001g0014 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0002t0001g0022 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0002t0001g0023 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0002t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0002t0001g0040 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0002t0001g0043 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0002t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0002t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0002t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0002t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0002t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0002t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0002t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0002t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0002t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0002t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0002t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0002t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0002t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0002t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0002t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0002t0005g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0002t0007g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0002t0009g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0002t0013g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0003t0001g0004 | 0/0 | 6 | 5 | 0 | 1 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0003t0001g0029 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0003t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0003t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0003t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0003t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0003t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0003t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0003t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0004t0001g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0004t0001g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0004t0001g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0004t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0004t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0004t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0004t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0004t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0004t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0005t0001g0026 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0005t0001g0027 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0005t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0005t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0005t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0005t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0005t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0005t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0005t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0005t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0005t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0007t0001g0038 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0007t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0007t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0007t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0007t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0008t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0008t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0008t0011g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0008t0012g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0009t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0009t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0010t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0010t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0011t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0011t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0001c0013t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0002c0006t0001g0024 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0002c0006t0001g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0002c0006t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0002c0006t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0002c0006t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0002c0006t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0003c0012t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| a0004c0014t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0011 | EUR | GBR | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0128 | EUR | GBR | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0020 | EUR | GBR | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG00140 | hp2 | a0002 | c0006 | t0001 | g0024 | EUR | GBR | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0070 | EUR | FIN | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG00280 | hp2 | a0001 | c0002 | t0001 | g0126 | EUR | FIN | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0049 | EUR | FIN | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0077 | EUR | FIN | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG00408 | hp2 | a0001 | c0002 | t0001 | g0039 | EAS | CHS | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | CHS | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG00423 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0156 | EAS | CHS | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | CHS | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0043 | EAS | CHS | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG00597 | hp2 | a0001 | c0002 | t0001 | g0158 | EAS | CHS | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | CHS | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG00621 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | CHS | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG00639 | hp1 | a0001 | c0005 | t0001 | g0055 | AMR | PUR | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG00642 | hp1 | a0001 | c0005 | t0001 | g0059 | AMR | PUR | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG00733 | hp1 | a0001 | c0002 | t0001 | g0013 | AMR | PUR | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG00738 | hp2 | a0002 | c0006 | t0001 | g0175 | AMR | PUR | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG01070 | hp1 | a0001 | c0002 | t0001 | g0022 | AMR | PUR | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG01070 | hp2 | a0001 | c0002 | t0001 | g0040 | AMR | PUR | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0134 | AMR | PUR | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0118 | AMR | PUR | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG01106 | hp2 | a0001 | c0002 | t0001 | g0165 | AMR | PUR | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG01109 | hp2 | a0001 | c0002 | t0001 | g0120 | AMR | PUR | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0022 | AMR | PUR | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG01168 | hp1 | a0001 | c0002 | t0001 | g0150 | AMR | PUR | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG01168 | hp2 | a0001 | c0005 | t0001 | g0058 | AMR | PUR | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG01175 | hp1 | a0001 | c0005 | t0001 | g0061 | AMR | PUR | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG01192 | hp1 | a0001 | c0005 | t0001 | g0062 | AMR | PUR | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG01255 | hp1 | a0001 | c0005 | t0001 | g0056 | AMR | CLM | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0178 | AMR | CLM | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG01256 | hp2 | a0001 | c0002 | t0001 | g0013 | AMR | CLM | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG01257 | hp1 | a0001 | c0005 | t0001 | g0027 | AMR | CLM | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG01261 | hp2 | a0001 | c0001 | t0014 | g0109 | AMR | CLM | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG01346 | hp2 | a0001 | c0005 | t0001 | g0026 | AMR | CLM | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | CLM | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0149 | AMR | CLM | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0152 | AMR | CLM | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | CLM | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0012 | AMR | CLM | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0078 | EUR | IBS | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG01516 | hp2 | a0001 | c0009 | t0001 | g0013 | EUR | IBS | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG01517 | hp1 | a0001 | c0001 | t0008 | g0019 | EUR | IBS | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG01517 | hp2 | a0001 | c0009 | t0001 | g0131 | EUR | IBS | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG01884 | hp1 | a0001 | c0003 | t0001 | g0004 | AFR | ACB | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0155 | AFR | ACB | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG01891 | hp1 | a0001 | c0003 | t0001 | g0004 | AFR | ACB | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG01891 | hp2 | a0001 | c0002 | t0001 | g0141 | AFR | ACB | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG01943 | hp1 | a0001 | c0002 | t0001 | g0043 | AMR | PEL | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG01975 | hp1 | a0001 | c0002 | t0001 | g0136 | AMR | PEL | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PEL | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PEL | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG01993 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02004 | hp1 | a0003 | c0012 | t0001 | g0001 | AMR | PEL | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02015 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02040 | hp1 | a0001 | c0005 | t0001 | g0027 | EAS | KHV | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0012 | AFR | ACB | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02055 | hp2 | a0001 | c0004 | t0001 | g0163 | AFR | ACB | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0014 | EAS | KHV | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02056 | hp2 | a0001 | c0001 | t0006 | g0099 | EAS | KHV | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02071 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0147 | EAS | KHV | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | KHV | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0133 | EAS | KHV | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | KHV | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02132 | hp2 | a0001 | c0002 | t0001 | g0039 | EAS | KHV | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0012 | AFR | ACB | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02145 | hp2 | a0001 | c0004 | t0001 | g0015 | AFR | ACB | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02148 | hp1 | a0001 | c0002 | t0001 | g0014 | AMR | PEL | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02148 | hp2 | a0001 | c0005 | t0001 | g0060 | AMR | PEL | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0053 | EAS | CDX | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CDX | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CDX | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | CDX | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0132 | AFR | ACB | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02257 | hp2 | a0001 | c0004 | t0001 | g0161 | AFR | ACB | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02273 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02280 | hp2 | a0001 | c0003 | t0001 | g0110 | AFR | ACB | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02451 | hp1 | a0001 | c0003 | t0001 | g0029 | AFR | ACB | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0037 | AFR | ACB | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0042 | EAS | KHV | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02615 | hp1 | a0001 | c0002 | t0001 | g0151 | AFR | GWD | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02630 | hp1 | a0001 | c0007 | t0001 | g0038 | AFR | GWD | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0121 | AFR | GWD | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02647 | hp1 | a0001 | c0001 | t0010 | g0167 | AFR | GWD | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02647 | hp2 | a0001 | c0003 | t0001 | g0071 | AFR | GWD | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0022 | SAS | PJL | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02717 | hp1 | a0001 | c0002 | t0007 | g0008 | AFR | GWD | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02717 | hp2 | a0001 | c0003 | t0001 | g0004 | AFR | GWD | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02723 | hp1 | a0001 | c0002 | t0001 | g0008 | AFR | GWD | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02723 | hp2 | a0001 | c0007 | t0001 | g0066 | AFR | GWD | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02735 | hp1 | a0001 | c0003 | t0001 | g0029 | SAS | PJL | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0014 | SAS | PJL | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02809 | hp2 | a0001 | c0002 | t0001 | g0008 | AFR | GWD | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02886 | hp1 | a0001 | c0003 | t0001 | g0004 | AFR | GWD | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02895 | hp1 | a0001 | c0001 | t0004 | g0067 | AFR | GWD | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02895 | hp2 | a0001 | c0002 | t0001 | g0023 | AFR | GWD | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02896 | hp2 | a0001 | c0002 | t0001 | g0001 | AFR | GWD | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02897 | hp1 | a0004 | c0014 | t0001 | g0125 | AFR | GWD | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | ESN | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02922 | hp2 | a0001 | c0004 | t0001 | g0045 | AFR | ESN | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02965 | hp1 | a0001 | c0004 | t0001 | g0045 | AFR | ESN | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02965 | hp2 | a0001 | c0002 | t0001 | g0008 | AFR | ESN | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02970 | hp1 | a0001 | c0003 | t0001 | g0030 | AFR | ESN | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | ESN | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02976 | hp2 | a0001 | c0002 | t0001 | g0012 | AFR | ESN | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0148 | SAS | PJL | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG03041 | hp2 | a0001 | c0002 | t0001 | g0153 | AFR | GWD | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | MSL | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0085 | AFR | MSL | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG03130 | hp1 | a0001 | c0001 | t0004 | g0068 | AFR | ESN | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG03130 | hp2 | a0001 | c0004 | t0001 | g0044 | AFR | ESN | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG03139 | hp1 | a0001 | c0007 | t0001 | g0114 | AFR | ESN | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG03139 | hp2 | a0001 | c0003 | t0001 | g0004 | AFR | ESN | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG03195 | hp1 | a0001 | c0004 | t0001 | g0159 | AFR | ESN | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG03195 | hp2 | a0001 | c0002 | t0001 | g0127 | AFR | ESN | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG03209 | hp1 | a0001 | c0007 | t0001 | g0113 | AFR | MSL | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG03209 | hp2 | a0001 | c0004 | t0001 | g0164 | AFR | MSL | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | MSL | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | MSL | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0135 | SAS | PJL | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | MSL | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG03486 | hp1 | a0001 | c0004 | t0001 | g0015 | AFR | MSL | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0008 | AFR | MSL | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG03491 | hp1 | a0001 | c0002 | t0009 | g0122 | SAS | PJL | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0037 | AFR | ESN | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | ESN | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0008 | AFR | MSL | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG03579 | hp2 | a0001 | c0004 | t0001 | g0160 | AFR | MSL | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG03654 | hp1 | a0001 | c0005 | t0001 | g0026 | SAS | PJL | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG03654 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG03704 | hp1 | a0001 | c0005 | t0001 | g0057 | SAS | PJL | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | BEB | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | BEB | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | BEB | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | BEB | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG03942 | hp1 | a0001 | c0002 | t0001 | g0013 | SAS | BEB | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0050 | SAS | BEB | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG04115 | hp1 | a0001 | c0002 | t0001 | g0140 | SAS | STU | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG04115 | hp2 | a0001 | c0011 | t0001 | g0116 | SAS | STU | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG04199 | hp1 | a0001 | c0003 | t0001 | g0073 | SAS | STU | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0119 | SAS | STU | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | YRI | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | YRI | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA18612 | hp1 | a0001 | c0010 | t0001 | g0002 | EAS | CHB | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA18612 | hp2 | a0001 | c0011 | t0001 | g0115 | EAS | CHB | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | CHB | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0137 | EAS | CHB | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA18906 | hp1 | a0001 | c0003 | t0001 | g0030 | AFR | YRI | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0105 | AFR | YRI | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA18943 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA18946 | hp1 | a0002 | c0006 | t0001 | g0172 | EAS | JPT | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA18946 | hp2 | a0001 | c0002 | t0001 | g0154 | EAS | JPT | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA18948 | hp1 | a0001 | c0007 | t0001 | g0166 | EAS | JPT | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA18950 | hp1 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA18950 | hp2 | a0002 | c0006 | t0001 | g0024 | EAS | JPT | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA18952 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA18954 | hp1 | a0001 | c0002 | t0001 | g0145 | EAS | JPT | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA18956 | hp1 | a0001 | c0008 | t0001 | g0002 | EAS | JPT | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA18956 | hp2 | a0001 | c0008 | t0011 | g0007 | EAS | JPT | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA18959 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA18961 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA18962 | hp1 | a0002 | c0006 | t0001 | g0171 | EAS | JPT | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA18966 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA18977 | hp1 | a0001 | c0002 | t0001 | g0146 | EAS | JPT | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA18984 | hp1 | a0001 | c0002 | t0001 | g0124 | EAS | JPT | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA18988 | hp1 | a0001 | c0008 | t0001 | g0001 | EAS | JPT | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA18988 | hp2 | a0002 | c0006 | t0001 | g0025 | EAS | JPT | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA19000 | hp1 | a0002 | c0006 | t0001 | g0174 | EAS | JPT | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA19000 | hp2 | a0001 | c0002 | t0001 | g0157 | EAS | JPT | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA19004 | hp1 | a0001 | c0002 | t0001 | g0129 | EAS | JPT | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA19005 | hp1 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA19007 | hp2 | a0001 | c0002 | t0001 | g0138 | EAS | JPT | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA19011 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA19011 | hp2 | a0002 | c0006 | t0001 | g0025 | EAS | JPT | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA19030 | hp1 | a0001 | c0003 | t0001 | g0111 | AFR | LWK | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | LWK | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA19043 | hp1 | a0001 | c0002 | t0001 | g0040 | AFR | LWK | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | LWK | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA19055 | hp1 | a0001 | c0002 | t0001 | g0130 | EAS | JPT | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA19055 | hp2 | a0002 | c0006 | t0001 | g0025 | EAS | JPT | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA19056 | hp2 | a0001 | c0008 | t0012 | g0001 | EAS | JPT | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA19058 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA19064 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA19066 | hp1 | a0001 | c0002 | t0005 | g0042 | EAS | JPT | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA19066 | hp2 | a0001 | c0007 | t0001 | g0038 | EAS | JPT | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA19068 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA19070 | hp2 | a0001 | c0010 | t0001 | g0142 | EAS | JPT | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA19072 | hp1 | a0001 | c0003 | t0001 | g0074 | EAS | JPT | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA19072 | hp2 | a0001 | c0002 | t0013 | g0144 | EAS | JPT | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA19080 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA19081 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA19088 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA19091 | hp2 | a0001 | c0002 | t0001 | g0023 | EAS | JPT | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0143 | AFR | ASW | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA20129 | hp2 | a0001 | c0003 | t0001 | g0112 | AFR | ASW | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0033 | EUR | TSI | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0076 | EUR | TSI | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0033 | EUR | TSI | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA20805 | hp2 | a0001 | c0005 | t0001 | g0054 | EUR | TSI | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA20905 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | GIH | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | GIH | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | ACB | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02109 | hp2 | a0001 | c0004 | t0001 | g0044 | AFR | ACB | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02486 | hp1 | a0001 | c0004 | t0001 | g0015 | AFR | ACB | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG03471 | hp1 | a0001 | c0004 | t0001 | g0015 | AFR | MSL | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA20300 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | USA | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA20300 | hp2 | a0001 | c0004 | t0001 | g0162 | AFR | USA | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA21309 | hp1 | a0001 | c0013 | t0001 | g0072 | AFR | LWK | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| NA21309 | hp2 | a0001 | c0002 | t0002 | g0023 | AFR | LWK | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0011 | REF | REF | SYNGAP1_chr6_33415065_33458689 | SYNGAP1 | chr6 | 33415065 | 33458689 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:33432712 | A | G | 1 | a0004 | 1 | HG02897.hp1 | missense_variant | MODERATE | c.415A>G | p.Ser139Gly | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 5/19 | 615/6015 | 415/4032 | 139/1343 | chr6 | 33432712 | |||
| chr6:33443686 | C | G | 1 | a0003 | 1 | HG02004.hp1 | missense_variant | MODERATE | c.3134C>G | p.Ala1045Gly | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 15/19 | 3334/6015 | 3134/4032 | 1045/1343 | chr6 | 33443686 | |||
| chr6:33443896 | T | C | 1 | a0002 | 9 | HG00140.hp2 HG00738.hp2 NA18946.hp1 others(6): Show |
missense_variant | MODERATE | c.3344T>C | p.Ile1115Thr | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 15/19 | 3544/6015 | 3344/4032 | 1115/1343 | chr6 | 33443896 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:33425806 | C | A | 1 | a0001c0009 | 2 | HG01516.hp2 HG01517.hp2 |
synonymous_variant | LOW | c.198C>A | p.Pro66Pro | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 3/19 | 398/6015 | 198/4032 | 66/1343 | chr6 | 33425806 | |||
| chr6:33425806 | C | T | 1 | a0001c0004 | 14 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(11): Show |
synonymous_variant | LOW | c.198C>T | p.Pro66Pro | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 3/19 | 398/6015 | 198/4032 | 66/1343 | chr6 | 33425806 | |||
| chr6:33438779 | A | G | 3 | a0001c0003 a0001c0007 a0001c0013 |
23 | HG01884.hp1 HG01891.hp1 HG02280.hp2 others(20): Show |
synonymous_variant | LOW | c.1536A>G | p.Glu512Glu | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 10/19 | 1736/6015 | 1536/4032 | 512/1343 | chr6 | 33438779 | |||
| chr6:33440765 | G | A | 6 | a0001c0002 a0001c0008 a0001c0009 others(3): Show |
112 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(109): Show |
synonymous_variant | LOW | c.1713G>A | p.Ser571Ser | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 11/19 | 1913/6015 | 1713/4032 | 571/1343 | chr6 | 33440765 | |||
| chr6:33440828 | A | G | 1 | a0001c0011 | 2 | HG04115.hp2 NA18612.hp2 |
synonymous_variant | LOW | c.1776A>G | p.Ser592Ser | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 11/19 | 1976/6015 | 1776/4032 | 592/1343 | chr6 | 33440828 | |||
| chr6:33440855 | G | A | 1 | a0001c0008 | 4 | NA18956.hp1 NA18956.hp2 NA18988.hp1 others(1): Show |
synonymous_variant | LOW | c.1803G>A | p.Ala601Ala | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 11/19 | 2003/6015 | 1803/4032 | 601/1343 | chr6 | 33440855 | |||
| chr6:33440903 | G | A | 1 | a0001c0005 | 13 | HG00639.hp1 HG00642.hp1 HG01168.hp2 others(10): Show |
synonymous_variant | LOW | c.1851G>A | p.Glu617Glu | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 11/19 | 2051/6015 | 1851/4032 | 617/1343 | chr6 | 33440903 | |||
| chr6:33441275 | G | A | 1 | a0001c0010 | 2 | NA18612.hp1 NA19070.hp2 |
synonymous_variant | LOW | c.2016G>A | p.Thr672Thr | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 12/19 | 2216/6015 | 2016/4032 | 672/1343 | chr6 | 33441275 | |||
| chr6:33443495 | C | T | 1 | a0001c0013 | 1 | NA21309.hp1 | synonymous_variant | LOW | c.2943C>T | p.Gly981Gly | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 15/19 | 3143/6015 | 2943/4032 | 981/1343 | chr6 | 33443495 | |||
| chr6:33443522 | C | T | 2 | a0001c0003 a0001c0013 |
17 | HG01884.hp1 HG01891.hp1 HG02280.hp2 others(14): Show |
synonymous_variant | LOW | c.2970C>T | p.Ser990Ser | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 15/19 | 3170/6015 | 2970/4032 | 990/1343 | chr6 | 33443522 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:33420068 | T | C | 1 | a0001c0002t0005 | 1 | NA19066.hp1 | 5_prime_UTR_variant | MODIFIER | c.-197T>C | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 1/19 | 197 | chr6 | 33420068 | ||||||
| chr6:33451999 | C | T | 1 | a0001c0001t0014 | 1 | HG01261.hp2 | 3_prime_UTR_variant | MODIFIER | c.*93C>T | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 19/19 | 93 | chr6 | 33451999 | ||||||
| chr6:33452002 | G | A | 1 | a0001c0001t0006 | 1 | HG02056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*96G>A | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 19/19 | 96 | chr6 | 33452002 | ||||||
| chr6:33452085 | A | G | 1 | a0001c0002t0013 | 1 | NA19072.hp2 | 3_prime_UTR_variant | MODIFIER | c.*179A>G | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 19/19 | 179 | chr6 | 33452085 | ||||||
| chr6:33452086 | C | A | 1 | a0001c0002t0013 | 1 | NA19072.hp2 | 3_prime_UTR_variant | MODIFIER | c.*180C>A | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 19/19 | 180 | chr6 | 33452086 | ||||||
| chr6:33452094 | C | T | 1 | a0001c0008t0012 | 1 | NA19056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*188C>T | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 19/19 | 188 | chr6 | 33452094 | ||||||
| chr6:33452160 | C | T | 1 | a0001c0001t0004 | 2 | HG02895.hp1 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*254C>T | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 19/19 | 254 | chr6 | 33452160 | ||||||
| chr6:33452171 | C | A | 1 | a0001c0002t0013 | 1 | NA19072.hp2 | 3_prime_UTR_variant | MODIFIER | c.*265C>A | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 19/19 | 265 | chr6 | 33452171 | ||||||
| chr6:33452463 | T | C | 2 | a0001c0001t0002 a0001c0002t0002 |
2 | HG03098.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*557T>C | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 19/19 | 557 | chr6 | 33452463 | ||||||
| chr6:33452680 | G | A | 1 | a0001c0002t0007 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*774G>A | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 19/19 | 774 | chr6 | 33452680 | ||||||
| chr6:33452785 | G | T | 1 | a0001c0002t0013 | 1 | NA19072.hp2 | 3_prime_UTR_variant | MODIFIER | c.*879G>T | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 19/19 | 879 | chr6 | 33452785 | ||||||
| chr6:33452786 | T | C | 1 | a0001c0002t0013 | 1 | NA19072.hp2 | 3_prime_UTR_variant | MODIFIER | c.*880T>C | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 19/19 | 880 | chr6 | 33452786 | ||||||
| chr6:33452854 | G | A | 1 | a0001c0001t0008 | 1 | HG01517.hp1 | 3_prime_UTR_variant | MODIFIER | c.*948G>A | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 19/19 | 948 | chr6 | 33452854 | ||||||
| chr6:33453125 | C | G | 1 | a0001c0008t0011 | 1 | NA18956.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1219C>G | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 19/19 | 1219 | chr6 | 33453125 | ||||||
| chr6:33453162 | G | A | 1 | a0001c0002t0009 | 1 | HG03491.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1256G>A | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 19/19 | 1256 | chr6 | 33453162 | ||||||
| chr6:33453232 | T | C | 1 | a0001c0001t0003 | 2 | HG02451.hp2 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1326T>C | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 19/19 | 1326 | chr6 | 33453232 | ||||||
| chr6:33453452 | T | C | 1 | a0001c0001t0010 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1546T>C | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 19/19 | 1546 | chr6 | 33453452 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:33420517 | G | A | 4 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(1): Show |
4 | HG00323.hp1 HG01106.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+186G>A | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 1/18 | chr6 | 33420517 | |||||||
| chr6:33420673 | A | G | 1 | a0001c0002t0001g0178 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.67+342A>G | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 1/18 | chr6 | 33420673 | |||||||
| chr6:33420767 | G | A | 1 | a0001c0001t0001g0051 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.67+436G>A | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 1/18 | chr6 | 33420767 | |||||||
| chr6:33420931 | A | G | 2 | a0001c0001t0001g0176 a0001c0001t0001g0177 |
2 | HG00642.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.67+600A>G | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 1/18 | chr6 | 33420931 | |||||||
| chr6:33420970 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.67+639G>A | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 1/18 | chr6 | 33420970 | |||||||
| chr6:33420995 | A | T | 2 | a0001c0001t0001g0176 a0001c0001t0001g0177 |
2 | HG00642.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.67+664A>T | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 1/18 | chr6 | 33420995 | |||||||
| chr6:33421117 | C | G | 10 | a0001c0001t0001g0024 a0001c0001t0001g0046 a0001c0001t0001g0170 others(7): Show |
14 | HG00140.hp2 HG00621.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.67+786C>G | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 1/18 | chr6 | 33421117 | |||||||
| chr6:33421227 | T | C | 1 | a0001c0002t0001g0053 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.67+896T>C | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 1/18 | chr6 | 33421227 | |||||||
| chr6:33421277 | A | G | 3 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0010g0167 |
3 | HG02647.hp1 HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.67+946A>G | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 1/18 | chr6 | 33421277 | |||||||
| chr6:33421437 | T | C | 15 | a0001c0001t0001g0028 a0001c0001t0001g0063 a0001c0001t0001g0064 others(12): Show |
18 | HG00639.hp1 HG00642.hp1 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.67+1106T>C | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 1/18 | chr6 | 33421437 | |||||||
| chr6:33421513 | A | T | 1 | a0001c0007t0001g0166 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.67+1182A>T | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 1/18 | chr6 | 33421513 | |||||||
| chr6:33421547 | C | T | 4 | a0001c0001t0001g0028 a0001c0001t0001g0063 a0001c0001t0001g0064 others(1): Show |
5 | NA18948.hp2 NA18961.hp2 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.67+1216C>T | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 1/18 | chr6 | 33421547 | |||||||
| chr6:33421552 | C | CTCTTTTC others(3): Show |
1 | a0001c0002t0001g0165 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.67+1225_67+1234dup others(10): Show |
SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr6 | 33421552 | ||||||
| chr6:33421567 | C | G | 15 | a0001c0001t0001g0028 a0001c0001t0001g0063 a0001c0001t0001g0064 others(12): Show |
18 | HG00639.hp1 HG00642.hp1 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.67+1236C>G | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 1/18 | chr6 | 33421567 | |||||||
| chr6:33421604 | G | T | 76 | a0001c0001t0001g0016 a0001c0001t0001g0041 a0001c0001t0001g0123 others(73): Show |
132 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.67+1273G>T | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 1/18 | chr6 | 33421604 | |||||||
| chr6:33421678 | T | A | 1 | a0001c0007t0001g0066 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.67+1347T>A | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 1/18 | chr6 | 33421678 | |||||||
| chr6:33421791 | G | T | 6 | a0001c0001t0001g0021 a0001c0001t0001g0117 a0001c0001t0001g0176 others(3): Show |
8 | HG00642.hp2 HG00741.hp1 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+1460G>T | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 1/18 | chr6 | 33421791 | |||||||
| chr6:33421826 | C | T | 23 | a0001c0001t0001g0028 a0001c0001t0001g0063 a0001c0001t0001g0064 others(20): Show |
27 | HG00639.hp1 HG00642.hp1 HG01168.hp2 others(24): Show |
intron_variant | MODIFIER | c.67+1495C>T | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 1/18 | chr6 | 33421826 | |||||||
| chr6:33421873 | T | C | 2 | a0001c0001t0004g0067 a0001c0001t0004g0068 |
2 | HG02895.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.67+1542T>C | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 1/18 | chr6 | 33421873 | |||||||
| chr6:33421880 | C | T | 1 | a0001c0001t0001g0051 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.67+1549C>T | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 1/18 | chr6 | 33421880 | |||||||
| chr6:33421924 | G | A | 3 | a0001c0003t0001g0110 a0001c0003t0001g0111 a0001c0003t0001g0112 |
3 | HG02280.hp2 NA19030.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.68-1553G>A | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 1/18 | chr6 | 33421924 | |||||||
| chr6:33422110 | A | T | 1 | a0001c0007t0001g0166 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.68-1367A>T | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 1/18 | chr6 | 33422110 | |||||||
| chr6:33422162 | C | T | 2 | a0001c0001t0001g0021 a0001c0001t0001g0117 |
4 | HG00741.hp1 HG02622.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-1315C>T | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 1/18 | chr6 | 33422162 | |||||||
| chr6:33422227 | CAG | C | 2 | a0001c0001t0001g0021 a0001c0001t0001g0117 |
4 | HG00741.hp1 HG02622.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-1247_68-1246del others(2): Show |
SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr6 | 33422227 | ||||||
| chr6:33422507 | G | A | 1 | a0001c0001t0001g0069 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.68-970G>A | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 1/18 | chr6 | 33422507 | |||||||
| chr6:33422531 | C | A | 1 | a0001c0007t0001g0166 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.68-946C>A | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 1/18 | chr6 | 33422531 | |||||||
| chr6:33422577 | A | G | 8 | a0001c0003t0001g0110 a0001c0003t0001g0111 a0001c0003t0001g0112 others(5): Show |
9 | HG02280.hp2 HG02630.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.68-900A>G | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 1/18 | chr6 | 33422577 | |||||||
| chr6:33422633 | T | A | 1 | a0001c0001t0001g0070 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.68-844T>A | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 1/18 | chr6 | 33422633 | |||||||
| chr6:33422834 | A | T | 1 | a0001c0001t0014g0109 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.68-643A>T | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 1/18 | chr6 | 33422834 | |||||||
| chr6:33422865 | G | A | 1 | a0001c0003t0001g0110 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.68-612G>A | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 1/18 | chr6 | 33422865 | |||||||
| chr6:33422977 | A | G | 1 | a0001c0001t0003g0037 | 2 | HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.68-500A>G | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 1/18 | chr6 | 33422977 | |||||||
| chr6:33423200 | C | G | 4 | a0001c0007t0001g0038 a0001c0007t0001g0113 a0001c0007t0001g0114 others(1): Show |
5 | HG02630.hp1 HG03139.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.68-277C>G | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 1/18 | chr6 | 33423200 | |||||||
| chr6:33423227 | T | A | 1 | a0001c0007t0001g0166 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.68-250T>A | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 1/18 | chr6 | 33423227 | |||||||
| chr6:33423398 | T | G | 7 | a0001c0003t0001g0004 a0001c0003t0001g0029 a0001c0003t0001g0030 others(4): Show |
14 | HG01884.hp1 HG01891.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.68-79T>G | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 1/18 | chr6 | 33423398 | |||||||
| chr6:33423401 | C | T | 10 | a0001c0001t0001g0016 a0001c0004t0001g0015 a0001c0004t0001g0044 others(7): Show |
18 | HG01123.hp1 HG02055.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.68-76C>T | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 1/18 | chr6 | 33423401 | |||||||
| chr6:33423627 | G | A | 2 | a0001c0001t0001g0021 a0001c0001t0001g0117 |
4 | HG00741.hp1 HG02622.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.189+29G>A | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 2/18 | chr6 | 33423627 | |||||||
| chr6:33423716 | G | A | 2 | a0001c0001t0001g0176 a0001c0001t0001g0177 |
2 | HG00642.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.189+118G>A | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 2/18 | chr6 | 33423716 | |||||||
| chr6:33423734 | T | A | 1 | a0001c0002t0001g0118 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.189+136T>A | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 2/18 | chr6 | 33423734 | |||||||
| chr6:33423773 | T | A | 1 | a0001c0007t0001g0166 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.189+175T>A | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 2/18 | chr6 | 33423773 | |||||||
| chr6:33424248 | G | C | 11 | a0001c0005t0001g0026 a0001c0005t0001g0027 a0001c0005t0001g0054 others(8): Show |
13 | HG00639.hp1 HG00642.hp1 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.189+650G>C | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 2/18 | chr6 | 33424248 | |||||||
| chr6:33424697 | G | A | 1 | a0001c0001t0001g0051 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.189+1099G>A | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 2/18 | chr6 | 33424697 | |||||||
| chr6:33424768 | G | A | 1 | a0001c0007t0001g0066 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.190-1030G>A | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 2/18 | chr6 | 33424768 | |||||||
| chr6:33424948 | G | A | 1 | a0001c0007t0001g0066 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.190-850G>A | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 2/18 | chr6 | 33424948 | |||||||
| chr6:33425151 | G | A | 1 | a0001c0007t0001g0066 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.190-647G>A | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 2/18 | chr6 | 33425151 | |||||||
| chr6:33425319 | C | T | 1 | a0001c0002t0001g0158 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.190-479C>T | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 2/18 | chr6 | 33425319 | |||||||
| chr6:33425594 | T | G | 1 | a0001c0007t0001g0166 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.190-204T>G | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 2/18 | chr6 | 33425594 | |||||||
| chr6:33425595 | G | T | 1 | a0001c0007t0001g0166 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.190-203G>T | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 2/18 | chr6 | 33425595 | |||||||
| chr6:33425614 | G | C | 1 | a0001c0002t0001g0119 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.190-184G>C | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 2/18 | chr6 | 33425614 | |||||||
| chr6:33425650 | A | G | 4 | a0001c0007t0001g0038 a0001c0007t0001g0113 a0001c0007t0001g0114 others(1): Show |
5 | HG02630.hp1 HG03139.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.190-148A>G | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 2/18 | chr6 | 33425650 | |||||||
| chr6:33425748 | G | A | 2 | a0001c0002t0001g0120 a0001c0002t0001g0121 |
2 | HG01109.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.190-50G>A | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 2/18 | chr6 | 33425748 | |||||||
| chr6:33425990 | G | T | 4 | a0001c0001t0001g0036 a0001c0001t0001g0106 a0001c0001t0001g0107 others(1): Show |
5 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.295+87G>T | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 3/18 | chr6 | 33425990 | |||||||
| chr6:33426131 | G | T | 1 | a0001c0007t0001g0066 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.295+228G>T | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 3/18 | chr6 | 33426131 | |||||||
| chr6:33426476 | C | G | 76 | a0001c0001t0001g0016 a0001c0001t0001g0041 a0001c0001t0001g0123 others(73): Show |
132 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.295+573C>G | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 3/18 | chr6 | 33426476 | |||||||
| chr6:33427183 | T | C | 2 | a0001c0001t0001g0031 a0001c0001t0001g0075 |
3 | HG00544.hp2 NA19007.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.295+1280T>C | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 3/18 | chr6 | 33427183 | |||||||
| chr6:33427422 | G | A | 76 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(73): Show |
117 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.295+1519G>A | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 3/18 | chr6 | 33427422 | |||||||
| chr6:33427503 | T | TA | 4 | a0001c0007t0001g0038 a0001c0007t0001g0113 a0001c0007t0001g0114 others(1): Show |
5 | HG02630.hp1 HG03139.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.295+1600_295+1601i others(3): Show |
SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 3/18 | chr6 | 33427503 | |||||||
| chr6:33427743 | T | G | 2 | a0001c0001t0001g0123 a0001c0007t0001g0066 |
2 | HG02723.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.295+1840T>G | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 3/18 | chr6 | 33427743 | |||||||
| chr6:33427745 | G | T | 44 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(41): Show |
72 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.295+1842G>T | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 3/18 | chr6 | 33427745 | |||||||
| chr6:33427774 | G | A | 1 | a0001c0003t0001g0071 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.295+1871G>A | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 3/18 | chr6 | 33427774 | |||||||
| chr6:33427986 | G | T | 2 | a0001c0001t0001g0003 a0001c0001t0001g0034 |
9 | HG02040.hp2 HG02074.hp2 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.295+2083G>T | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 3/18 | chr6 | 33427986 | |||||||
| chr6:33428168 | A | AG | 14 | a0001c0001t0001g0050 a0001c0001t0001g0104 a0001c0001t0001g0117 others(11): Show |
18 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(15): Show |
intron_variant | MODIFIER | c.295+2273dupG | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr6 | 33428168 | ||||||
| chr6:33428193 | C | CG | 5 | a0001c0001t0001g0117 a0001c0001t0001g0169 a0001c0002t0001g0157 others(2): Show |
5 | HG00741.hp1 HG01192.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.295+2295dupG | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr6 | 33428193 | ||||||
| chr6:33428319 | C | T | 15 | a0001c0001t0001g0028 a0001c0001t0001g0063 a0001c0001t0001g0064 others(12): Show |
18 | HG00639.hp1 HG00642.hp1 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.295+2416C>T | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 3/18 | chr6 | 33428319 | |||||||
| chr6:33428322 | A | C | 2 | a0001c0001t0004g0067 a0001c0001t0004g0068 |
2 | HG02895.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.295+2419A>C | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 3/18 | chr6 | 33428322 | |||||||
| chr6:33428374 | T | C | 1 | a0001c0001t0001g0076 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.295+2471T>C | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 3/18 | chr6 | 33428374 | |||||||
| chr6:33428438 | C | T | 9 | a0001c0005t0001g0026 a0001c0005t0001g0027 a0001c0005t0001g0056 others(6): Show |
11 | HG00642.hp1 HG01168.hp2 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.295+2535C>T | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 3/18 | chr6 | 33428438 | |||||||
| chr6:33428538 | T | G | 187 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(184): Show |
299 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.295+2635T>G | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 3/18 | chr6 | 33428538 | |||||||
| chr6:33428872 | G | A | 1 | a0001c0005t0001g0056 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.295+2969G>A | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 3/18 | chr6 | 33428872 | |||||||
| chr6:33428899 | T | C | 1 | a0001c0005t0001g0062 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.295+2996T>C | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 3/18 | chr6 | 33428899 | |||||||
| chr6:33429519 | G | A | 2 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.296-2642G>A | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 3/18 | chr6 | 33429519 | |||||||
| chr6:33429593 | A | G | 1 | a0001c0002t0001g0118 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.296-2568A>G | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 3/18 | chr6 | 33429593 | |||||||
| chr6:33429817 | C | T | 1 | a0001c0004t0001g0045 | 2 | HG02922.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.296-2344C>T | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 3/18 | chr6 | 33429817 | |||||||
| chr6:33429818 | G | A | 2 | a0001c0001t0001g0176 a0001c0001t0001g0177 |
2 | HG00642.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.296-2343G>A | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 3/18 | chr6 | 33429818 | |||||||
| chr6:33429904 | T | C | 1 | a0001c0005t0001g0057 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.296-2257T>C | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 3/18 | chr6 | 33429904 | |||||||
| chr6:33430019 | G | A | 2 | a0001c0002t0001g0124 a0001c0002t0009g0122 |
2 | HG03491.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.296-2142G>A | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 3/18 | chr6 | 33430019 | |||||||
| chr6:33430140 | C | G | 1 | a0001c0002t0001g0155 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.296-2021C>G | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 3/18 | chr6 | 33430140 | |||||||
| chr6:33430189 | C | T | 5 | a0001c0001t0001g0010 a0001c0001t0001g0035 a0001c0001t0001g0101 others(2): Show |
9 | HG01192.hp2 HG01243.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.296-1972C>T | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 3/18 | chr6 | 33430189 | |||||||
| chr6:33430427 | G | A | 2 | a0001c0002t0001g0118 a0001c0002t0001g0155 |
2 | HG01099.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.296-1734G>A | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 3/18 | chr6 | 33430427 | |||||||
| chr6:33430665 | C | T | 2 | a0001c0001t0001g0168 a0001c0001t0001g0169 |
2 | HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.296-1496C>T | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 3/18 | chr6 | 33430665 | |||||||
| chr6:33430843 | T | C | 180 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(177): Show |
291 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.296-1318T>C | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 3/18 | chr6 | 33430843 | |||||||
| chr6:33430900 | C | T | 1 | a0001c0002t0001g0154 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.296-1261C>T | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 3/18 | chr6 | 33430900 | |||||||
| chr6:33430972 | G | A | 1 | a0001c0001t0002g0085 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.296-1189G>A | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 3/18 | chr6 | 33430972 | |||||||
| chr6:33431209 | C | T | 1 | a0001c0001t0001g0049 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.296-952C>T | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 3/18 | chr6 | 33431209 | |||||||
| chr6:33431422 | C | T | 1 | a0001c0002t0001g0153 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.296-739C>T | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 3/18 | chr6 | 33431422 | |||||||
| chr6:33431502 | T | A | 1 | a0004c0014t0001g0125 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.296-659T>A | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 3/18 | chr6 | 33431502 | |||||||
| chr6:33431609 | T | G | 1 | a0001c0013t0001g0072 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.296-552T>G | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 3/18 | chr6 | 33431609 | |||||||
| chr6:33431827 | C | A | 2 | a0001c0002t0001g0120 a0001c0002t0001g0121 |
2 | HG01109.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.296-334C>A | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 3/18 | chr6 | 33431827 | |||||||
| chr6:33431879 | C | T | 1 | a0001c0002t0001g0152 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.296-282C>T | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 3/18 | chr6 | 33431879 | |||||||
| chr6:33431900 | C | A | 1 | a0004c0014t0001g0125 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.296-261C>A | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 3/18 | chr6 | 33431900 | |||||||
| chr6:33432001 | C | T | 42 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(39): Show |
75 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.296-160C>T | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 3/18 | chr6 | 33432001 | |||||||
| chr6:33432284 | G | A | 4 | a0001c0007t0001g0038 a0001c0007t0001g0113 a0001c0007t0001g0114 others(1): Show |
5 | HG02630.hp1 HG03139.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.387+32G>A | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 4/18 | chr6 | 33432284 | |||||||
| chr6:33432319 | G | A | 4 | a0001c0007t0001g0038 a0001c0007t0001g0113 a0001c0007t0001g0114 others(1): Show |
5 | HG02630.hp1 HG03139.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.387+67G>A | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 4/18 | chr6 | 33432319 | |||||||
| chr6:33432365 | A | G | 1 | a0004c0014t0001g0125 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.387+113A>G | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 4/18 | chr6 | 33432365 | |||||||
| chr6:33432366 | G | A | 1 | a0004c0014t0001g0125 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.387+114G>A | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 4/18 | chr6 | 33432366 | |||||||
| chr6:33432367 | A | G | 1 | a0004c0014t0001g0125 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.387+115A>G | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 4/18 | chr6 | 33432367 | |||||||
| chr6:33432512 | C | A | 8 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0090 others(5): Show |
17 | HG00639.hp2 HG01256.hp1 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.388-173C>A | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 4/18 | chr6 | 33432512 | |||||||
| chr6:33432565 | C | T | 4 | a0001c0001t0001g0028 a0001c0001t0001g0063 a0001c0001t0001g0064 others(1): Show |
5 | NA18948.hp2 NA18961.hp2 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.388-120C>T | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 4/18 | chr6 | 33432565 | |||||||
| chr6:33433054 | GAGGGACT others(4): Show |
G | 1 | a0001c0002t0001g0039 | 2 | HG00408.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.509+263_509+273del others(11): Show |
SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr6 | 33433054 | ||||||
| chr6:33433066 | A | G | 1 | a0001c0001t0001g0098 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.509+260A>G | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 5/18 | chr6 | 33433066 | |||||||
| chr6:33433124 | G | A | 1 | a0001c0007t0001g0066 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.509+318G>A | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 5/18 | chr6 | 33433124 | |||||||
| chr6:33433272 | A | G | 1 | a0001c0002t0001g0053 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.509+466A>G | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 5/18 | chr6 | 33433272 | |||||||
| chr6:33433347 | C | G | 77 | a0001c0001t0001g0016 a0001c0001t0001g0041 a0001c0001t0001g0123 others(74): Show |
133 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.509+541C>G | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 5/18 | chr6 | 33433347 | |||||||
| chr6:33433381 | C | T | 11 | a0001c0005t0001g0026 a0001c0005t0001g0027 a0001c0005t0001g0054 others(8): Show |
13 | HG00639.hp1 HG00642.hp1 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.509+575C>T | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 5/18 | chr6 | 33433381 | |||||||
| chr6:33433416 | G | T | 1 | a0001c0001t0001g0103 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.509+610G>T | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 5/18 | chr6 | 33433416 | |||||||
| chr6:33433461 | C | T | 2 | a0001c0011t0001g0115 a0001c0011t0001g0116 |
2 | HG04115.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.509+655C>T | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 5/18 | chr6 | 33433461 | |||||||
| chr6:33433514 | C | A | 5 | a0001c0002t0001g0040 a0001c0002t0001g0120 a0001c0002t0001g0121 others(2): Show |
6 | HG00280.hp2 HG01070.hp2 HG01109.hp2 others(3): Show |
intron_variant | MODIFIER | c.509+708C>A | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 5/18 | chr6 | 33433514 | |||||||
| chr6:33433634 | C | G | 1 | a0001c0001t0001g0093 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.509+828C>G | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 5/18 | chr6 | 33433634 | |||||||
| chr6:33433703 | C | CG | 76 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0018 others(73): Show |
112 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.509+908dupG | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr6 | 33433703 | ||||||
| chr6:33433703 | C | G | 1 | a0001c0002t0001g0151 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.509+897C>G | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 5/18 | chr6 | 33433703 | |||||||
| chr6:33433703 | CG | C | 21 | a0001c0001t0001g0010 a0001c0001t0001g0035 a0001c0001t0001g0100 others(18): Show |
31 | HG01109.hp2 HG01168.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.509+908delG | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr6 | 33433703 | ||||||
| chr6:33433704 | G | A | 1 | a0001c0002t0001g0128 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.509+898G>A | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 5/18 | chr6 | 33433704 | |||||||
| chr6:33433704 | G | C | 1 | a0001c0007t0001g0066 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.509+898G>C | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 5/18 | chr6 | 33433704 | |||||||
| chr6:33433706 | G | T | 4 | a0001c0007t0001g0038 a0001c0007t0001g0113 a0001c0007t0001g0114 others(1): Show |
5 | HG02630.hp1 HG03139.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.509+900G>T | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 5/18 | chr6 | 33433706 | |||||||
| chr6:33433724 | CG | C | 15 | a0001c0001t0001g0028 a0001c0001t0001g0063 a0001c0001t0001g0064 others(12): Show |
18 | HG00639.hp1 HG00642.hp1 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.509+923delG | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr6 | 33433724 | ||||||
| chr6:33433760 | G | C | 2 | a0001c0001t0001g0046 a0001c0001t0001g0170 |
3 | HG02027.hp2 HG02129.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.509+954G>C | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 5/18 | chr6 | 33433760 | |||||||
| chr6:33433984 | G | A | 2 | a0001c0003t0001g0110 a0001c0003t0001g0111 |
2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.510-1168G>A | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 5/18 | chr6 | 33433984 | |||||||
| chr6:33434051 | C | A | 10 | a0001c0001t0001g0016 a0001c0004t0001g0015 a0001c0004t0001g0044 others(7): Show |
18 | HG01123.hp1 HG02055.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.510-1101C>A | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 5/18 | chr6 | 33434051 | |||||||
| chr6:33434095 | G | C | 187 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(184): Show |
299 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.510-1057G>C | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 5/18 | chr6 | 33434095 | |||||||
| chr6:33434304 | CT | C | 11 | a0001c0003t0001g0004 a0001c0003t0001g0029 a0001c0003t0001g0030 others(8): Show |
18 | HG01884.hp1 HG01891.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.510-845delT | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr6 | 33434304 | ||||||
| chr6:33434309 | C | T | 11 | a0001c0003t0001g0004 a0001c0003t0001g0029 a0001c0003t0001g0030 others(8): Show |
18 | HG01884.hp1 HG01891.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.510-843C>T | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 5/18 | chr6 | 33434309 | |||||||
| chr6:33434399 | CT | C | 61 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(58): Show |
99 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.510-741delT | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr6 | 33434399 | ||||||
| chr6:33434490 | G | A | 3 | a0001c0005t0001g0058 a0001c0005t0001g0061 a0001c0005t0001g0062 |
3 | HG01168.hp2 HG01175.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.510-662G>A | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 5/18 | chr6 | 33434490 | |||||||
| chr6:33434510 | CT | C | 177 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(174): Show |
289 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.510-629delT | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr6 | 33434510 | ||||||
| chr6:33434510 | CTT | C | 8 | a0001c0001t0001g0064 a0001c0001t0001g0077 a0001c0001t0001g0168 others(5): Show |
8 | HG00323.hp2 HG03225.hp1 HG03516.hp2 others(5): Show |
intron_variant | MODIFIER | c.510-630_510-629del others(2): Show |
SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr6 | 33434510 | ||||||
| chr6:33434608 | T | C | 1 | a0001c0001t0001g0036 | 2 | HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.510-544T>C | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 5/18 | chr6 | 33434608 | |||||||
| chr6:33434693 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.510-459G>A | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 5/18 | chr6 | 33434693 | |||||||
| chr6:33434825 | C | G | 1 | a0001c0002t0001g0154 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.510-327C>G | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 5/18 | chr6 | 33434825 | |||||||
| chr6:33434828 | G | C | 1 | a0001c0002t0001g0154 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.510-324G>C | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 5/18 | chr6 | 33434828 | |||||||
| chr6:33434925 | G | A | 2 | a0001c0001t0001g0090 a0001c0001t0001g0096 |
2 | HG01167.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.510-227G>A | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 5/18 | chr6 | 33434925 | |||||||
| chr6:33434941 | C | CA | 9 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0002t0001g0124 others(6): Show |
10 | HG00642.hp1 HG01257.hp1 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.510-199dupA | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr6 | 33434941 | ||||||
| chr6:33434941 | C | CAAAAAAA | 10 | a0001c0003t0001g0004 a0001c0003t0001g0029 a0001c0003t0001g0030 others(7): Show |
17 | HG01884.hp1 HG01891.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.510-205_510-199dup others(7): Show |
SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr6 | 33434941 | ||||||
| chr6:33434941 | C | CAAAAAAA others(1): Show |
5 | a0001c0003t0001g0073 a0001c0007t0001g0038 a0001c0007t0001g0066 others(2): Show |
6 | HG02630.hp1 HG02723.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.510-206_510-199dup others(8): Show |
SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr6 | 33434941 | ||||||
| chr6:33434955 | A | G | 1 | a0001c0002t0001g0154 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.510-197A>G | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 5/18 | chr6 | 33434955 | |||||||
| chr6:33435018 | C | T | 1 | a0001c0002t0001g0135 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.510-134C>T | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 5/18 | chr6 | 33435018 | |||||||
| chr6:33435075 | C | CA | 114 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(111): Show |
201 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.510-53dupA | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr6 | 33435075 | ||||||
| chr6:33435075 | C | CAA | 43 | a0001c0001t0001g0010 a0001c0001t0001g0016 a0001c0001t0001g0035 others(40): Show |
64 | HG00423.hp1 HG00621.hp1 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.510-54_510-53dupAA | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr6 | 33435075 | ||||||
| chr6:33435075 | C | CAAA | 11 | a0001c0001t0001g0088 a0001c0001t0001g0101 a0001c0001t0001g0104 others(8): Show |
13 | HG00642.hp2 HG00733.hp1 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.510-55_510-53dupAA others(1): Show |
SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr6 | 33435075 | ||||||
| chr6:33435075 | CAAAAAAA others(4): Show |
C | 1 | a0001c0002t0001g0146 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.510-63_510-53delAA others(9): Show |
SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr6 | 33435075 | ||||||
| chr6:33435100 | G | A | 14 | a0001c0003t0001g0004 a0001c0003t0001g0029 a0001c0003t0001g0030 others(11): Show |
21 | HG01884.hp1 HG01891.hp1 HG02280.hp2 others(18): Show |
intron_variant | MODIFIER | c.510-52G>A | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 5/18 | chr6 | 33435100 | |||||||
| chr6:33435102 | A | G | 10 | a0001c0003t0001g0004 a0001c0003t0001g0029 a0001c0003t0001g0030 others(7): Show |
17 | HG01884.hp1 HG01891.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.510-50A>G | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 5/18 | chr6 | 33435102 | |||||||
| chr6:33435474 | C | T | 1 | a0001c0002t0001g0132 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.664-41C>T | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 6/18 | chr6 | 33435474 | |||||||
| chr6:33435645 | C | T | 64 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0008 others(61): Show |
111 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.762+32C>T | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 7/18 | chr6 | 33435645 | |||||||
| chr6:33435792 | C | G | 2 | a0001c0001t0001g0069 a0001c0001t0001g0095 |
2 | HG03239.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.762+179C>G | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 7/18 | chr6 | 33435792 | |||||||
| chr6:33435931 | C | T | 15 | a0001c0001t0001g0028 a0001c0001t0001g0063 a0001c0001t0001g0064 others(12): Show |
18 | HG00639.hp1 HG00642.hp1 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.762+318C>T | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 7/18 | chr6 | 33435931 | |||||||
| chr6:33435948 | A | G | 1 | a0001c0001t0001g0084 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.762+335A>G | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 7/18 | chr6 | 33435948 | |||||||
| chr6:33436056 | A | T | 2 | a0001c0001t0001g0176 a0001c0001t0001g0177 |
2 | HG00642.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.762+443A>T | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 7/18 | chr6 | 33436056 | |||||||
| chr6:33436158 | A | T | 2 | a0001c0001t0001g0087 a0001c0001t0001g0088 |
2 | HG02080.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.762+545A>T | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 7/18 | chr6 | 33436158 | |||||||
| chr6:33436283 | T | A | 1 | a0001c0010t0001g0142 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.762+670T>A | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 7/18 | chr6 | 33436283 | |||||||
| chr6:33436287 | G | A | 42 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(39): Show |
75 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.762+674G>A | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 7/18 | chr6 | 33436287 | |||||||
| chr6:33436320 | C | CT | 13 | a0001c0001t0001g0035 a0001c0001t0001g0101 a0001c0001t0001g0107 others(10): Show |
21 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.762+723dupT | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr6 | 33436320 | ||||||
| chr6:33436664 | T | C | 1 | a0001c0007t0001g0066 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.763-1004T>C | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 7/18 | chr6 | 33436664 | |||||||
| chr6:33436702 | C | A | 2 | a0001c0011t0001g0115 a0001c0011t0001g0116 |
2 | HG04115.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.763-966C>A | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 7/18 | chr6 | 33436702 | |||||||
| chr6:33437058 | G | C | 2 | a0001c0001t0001g0102 a0001c0001t0001g0104 |
2 | HG01192.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.763-610G>C | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 7/18 | chr6 | 33437058 | |||||||
| chr6:33437403 | G | A | 10 | a0001c0003t0001g0004 a0001c0003t0001g0029 a0001c0003t0001g0030 others(7): Show |
17 | HG01884.hp1 HG01891.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.763-265G>A | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 7/18 | chr6 | 33437403 | |||||||
| chr6:33437546 | C | T | 4 | a0001c0001t0001g0036 a0001c0001t0001g0106 a0001c0001t0001g0107 others(1): Show |
5 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.763-122C>T | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 7/18 | chr6 | 33437546 | |||||||
| chr6:33438351 | T | C | 1 | a0001c0001t0002g0085 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1386+60T>C | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 8/18 | chr6 | 33438351 | |||||||
| chr6:33438615 | C | T | 4 | a0001c0001t0001g0019 a0001c0001t0001g0079 a0001c0001t0001g0082 others(1): Show |
5 | HG01123.hp2 HG01243.hp1 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.1531+52C>T | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 9/18 | chr6 | 33438615 | |||||||
| chr6:33438628 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1531+65C>T | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 9/18 | chr6 | 33438628 | |||||||
| chr6:33438721 | C | T | 1 | a0001c0007t0001g0066 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1532-54C>T | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 9/18 | chr6 | 33438721 | |||||||
| chr6:33439119 | G | GA | 12 | a0001c0001t0001g0102 a0001c0003t0001g0004 a0001c0003t0001g0029 others(9): Show |
19 | HG01884.hp1 HG01891.hp1 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.1676+213dupA | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr6 | 33439119 | ||||||
| chr6:33439272 | G | A | 1 | a0001c0003t0001g0030 | 2 | HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1676+353G>A | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 10/18 | chr6 | 33439272 | |||||||
| chr6:33439483 | A | C | 3 | a0001c0001t0001g0018 a0001c0001t0001g0078 a0001c0001t0001g0083 |
5 | HG00733.hp2 HG00738.hp1 HG00741.hp2 others(2): Show |
intron_variant | MODIFIER | c.1676+564A>C | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 10/18 | chr6 | 33439483 | |||||||
| chr6:33439532 | G | A | 2 | a0001c0001t0001g0176 a0001c0001t0001g0177 |
2 | HG00642.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.1676+613G>A | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 10/18 | chr6 | 33439532 | |||||||
| chr6:33439606 | C | G | 1 | a0001c0001t0010g0167 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1676+687C>G | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 10/18 | chr6 | 33439606 | |||||||
| chr6:33439810 | G | C | 187 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(184): Show |
299 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.1676+891G>C | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 10/18 | chr6 | 33439810 | |||||||
| chr6:33439847 | A | G | 187 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(184): Show |
299 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.1677-882A>G | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 10/18 | chr6 | 33439847 | |||||||
| chr6:33439862 | A | C | 1 | a0001c0007t0001g0066 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1677-867A>C | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 10/18 | chr6 | 33439862 | |||||||
| chr6:33439926 | T | C | 2 | a0001c0011t0001g0115 a0001c0011t0001g0116 |
2 | HG04115.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.1677-803T>C | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 10/18 | chr6 | 33439926 | |||||||
| chr6:33439945 | G | A | 1 | a0001c0007t0001g0114 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1677-784G>A | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 10/18 | chr6 | 33439945 | |||||||
| chr6:33440018 | G | C | 1 | a0001c0001t0001g0092 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1677-711G>C | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 10/18 | chr6 | 33440018 | |||||||
| chr6:33440132 | T | C | 2 | a0001c0001t0004g0067 a0001c0001t0004g0068 |
2 | HG02895.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1677-597T>C | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 10/18 | chr6 | 33440132 | |||||||
| chr6:33440267 | G | T | 1 | a0001c0001t0001g0092 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1677-462G>T | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 10/18 | chr6 | 33440267 | |||||||
| chr6:33440493 | C | T | 1 | a0001c0001t0001g0092 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1677-236C>T | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 10/18 | chr6 | 33440493 | |||||||
| chr6:33440494 | T | C | 1 | a0001c0001t0001g0092 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1677-235T>C | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 10/18 | chr6 | 33440494 | |||||||
| chr6:33440555 | T | C | 1 | a0001c0001t0001g0092 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1677-174T>C | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 10/18 | chr6 | 33440555 | |||||||
| chr6:33440556 | C | T | 1 | a0001c0001t0001g0092 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1677-173C>T | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 10/18 | chr6 | 33440556 | |||||||
| chr6:33440688 | T | C | 1 | a0001c0007t0001g0066 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1677-41T>C | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 10/18 | chr6 | 33440688 | |||||||
| chr6:33440986 | GGGCAGGG others(8): Show |
G | 16 | a0001c0001t0001g0028 a0001c0001t0001g0063 a0001c0001t0001g0064 others(13): Show |
19 | HG00639.hp1 HG00642.hp1 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.1913+45_1913+59del others(15): Show |
SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr6 | 33440986 | ||||||
| chr6:33441033 | G | T | 1 | a0001c0007t0001g0066 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1913+68G>T | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 11/18 | chr6 | 33441033 | |||||||
| chr6:33441093 | GTGTGTGT others(3): Show |
G | 10 | a0001c0001t0001g0098 a0001c0004t0001g0015 a0001c0004t0001g0044 others(7): Show |
15 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.1914-60_1914-51del others(10): Show |
SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr6 | 33441093 | ||||||
| chr6:33441113 | A | ATG | 13 | a0001c0001t0001g0006 a0001c0001t0001g0028 a0001c0001t0001g0033 others(10): Show |
14 | HG00639.hp2 HG00642.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.1914-34_1914-33dup others(2): Show |
SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr6 | 33441113 | ||||||
| chr6:33441113 | A | ATGTG | 3 | a0001c0001t0001g0063 a0001c0001t0004g0067 a0001c0001t0004g0068 |
3 | HG02895.hp1 HG03130.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.1914-36_1914-33dup others(4): Show |
SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr6 | 33441113 | ||||||
| chr6:33441113 | A | G | 1 | a0001c0002t0001g0158 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1914-60A>G | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 11/18 | chr6 | 33441113 | |||||||
| chr6:33441113 | ATGTG | A | 11 | a0001c0001t0001g0010 a0001c0001t0001g0035 a0001c0001t0001g0101 others(8): Show |
15 | HG01175.hp1 HG01192.hp1 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.1914-36_1914-33del others(4): Show |
SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr6 | 33441113 | ||||||
| chr6:33441113 | ATGTGTGT others(1): Show |
A | 3 | a0001c0007t0001g0038 a0001c0007t0001g0114 a0001c0007t0001g0166 |
4 | HG02630.hp1 HG03139.hp1 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.1914-40_1914-33del others(8): Show |
SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr6 | 33441113 | ||||||
| chr6:33441125 | G | A | 2 | a0001c0002t0001g0137 a0001c0002t0001g0156 |
2 | HG00544.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.1914-48G>A | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 11/18 | chr6 | 33441125 | |||||||
| chr6:33441489 | A | G | 1 | a0001c0002t0009g0122 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2116-92A>G | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 12/18 | chr6 | 33441489 | |||||||
| chr6:33441960 | T | G | 21 | a0001c0001t0001g0021 a0001c0001t0001g0117 a0001c0001t0001g0176 others(18): Show |
31 | HG00642.hp2 HG00741.hp1 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.2294+201T>G | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 13/18 | chr6 | 33441960 | |||||||
| chr6:33442244 | G | T | 2 | a0001c0001t0001g0102 a0001c0001t0001g0104 |
2 | HG01192.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2295-209G>T | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 13/18 | chr6 | 33442244 | |||||||
| chr6:33442285 | C | T | 15 | a0001c0001t0001g0028 a0001c0001t0001g0063 a0001c0001t0001g0064 others(12): Show |
18 | HG00639.hp1 HG00642.hp1 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.2295-168C>T | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 13/18 | chr6 | 33442285 | |||||||
| chr6:33442362 | T | C | 11 | a0001c0005t0001g0026 a0001c0005t0001g0027 a0001c0005t0001g0054 others(8): Show |
13 | HG00639.hp1 HG00642.hp1 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.2295-91T>C | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 13/18 | chr6 | 33442362 | |||||||
| chr6:33442428 | C | T | 1 | a0001c0002t0001g0105 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2295-25C>T | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 13/18 | chr6 | 33442428 | |||||||
| chr6:33442735 | T | G | 1 | a0001c0002t0001g0128 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2337-154T>G | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 14/18 | chr6 | 33442735 | |||||||
| chr6:33444022 | G | A | 1 | a0001c0002t0001g0165 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.3408+62G>A | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 15/18 | chr6 | 33444022 | |||||||
| chr6:33444140 | A | T | 1 | a0001c0002t0001g0128 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.3408+180A>T | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 15/18 | chr6 | 33444140 | |||||||
| chr6:33444164 | C | T | 1 | a0001c0003t0001g0111 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3408+204C>T | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 15/18 | chr6 | 33444164 | |||||||
| chr6:33444201 | G | A | 4 | a0001c0001t0001g0028 a0001c0001t0001g0063 a0001c0001t0001g0064 others(1): Show |
5 | NA18948.hp2 NA18961.hp2 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.3408+241G>A | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 15/18 | chr6 | 33444201 | |||||||
| chr6:33444420 | C | T | 5 | a0001c0001t0001g0010 a0001c0001t0001g0035 a0001c0001t0001g0101 others(2): Show |
9 | HG01192.hp2 HG01243.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.3409-24C>T | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 15/18 | chr6 | 33444420 | |||||||
| chr6:33444752 | G | C | 1 | a0001c0003t0001g0071 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3582+135G>C | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 16/18 | chr6 | 33444752 | |||||||
| chr6:33445108 | T | C | 1 | a0001c0001t0001g0098 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.3582+491T>C | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 16/18 | chr6 | 33445108 | |||||||
| chr6:33445115 | C | A | 5 | a0001c0001t0001g0010 a0001c0001t0001g0035 a0001c0001t0001g0101 others(2): Show |
9 | HG01192.hp2 HG01243.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.3582+498C>A | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 16/18 | chr6 | 33445115 | |||||||
| chr6:33445230 | G | A | 5 | a0001c0002t0001g0022 a0001c0002t0001g0134 a0001c0002t0001g0140 others(2): Show |
7 | HG01070.hp1 HG01081.hp2 HG01167.hp2 others(4): Show |
intron_variant | MODIFIER | c.3582+613G>A | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 16/18 | chr6 | 33445230 | |||||||
| chr6:33445235 | C | T | 1 | a0001c0007t0001g0066 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3582+618C>T | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 16/18 | chr6 | 33445235 | |||||||
| chr6:33445242 | A | C | 36 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0063 others(33): Show |
48 | HG00639.hp1 HG00642.hp1 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.3582+625A>C | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 16/18 | chr6 | 33445242 | |||||||
| chr6:33445477 | A | AT | 187 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(184): Show |
299 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.3582+869dupT | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr6 | 33445477 | ||||||
| chr6:33445538 | T | G | 2 | a0001c0001t0001g0010 a0001c0001t0001g0101 |
5 | HG01243.hp2 HG02280.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.3582+921T>G | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 16/18 | chr6 | 33445538 | |||||||
| chr6:33445713 | G | A | 1 | a0001c0001t0001g0139 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3583-862G>A | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 16/18 | chr6 | 33445713 | |||||||
| chr6:33445719 | A | C | 1 | a0001c0001t0001g0033 | 2 | NA20752.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.3583-856A>C | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 16/18 | chr6 | 33445719 | |||||||
| chr6:33445815 | TTTTC | T | 30 | a0001c0001t0001g0016 a0001c0001t0001g0041 a0001c0001t0001g0123 others(27): Show |
51 | HG00280.hp2 HG00733.hp1 HG01070.hp1 others(48): Show |
intron_variant | MODIFIER | c.3583-756_3583-753d others(6): Show |
SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr6 | 33445815 | ||||||
| chr6:33445816 | TTTC | T | 44 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0014 others(41): Show |
74 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.3583-756_3583-754d others(5): Show |
SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr6 | 33445816 | ||||||
| chr6:33445819 | C | CT | 18 | a0001c0001t0001g0018 a0001c0001t0001g0028 a0001c0001t0001g0170 others(15): Show |
27 | HG00741.hp2 HG01099.hp1 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.3583-734dupT | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr6 | 33445819 | ||||||
| chr6:33445819 | C | CTT | 18 | a0001c0001t0001g0028 a0001c0001t0001g0063 a0001c0001t0001g0064 others(15): Show |
19 | HG00639.hp1 HG00642.hp1 HG00642.hp2 others(16): Show |
intron_variant | MODIFIER | c.3583-735_3583-734d others(4): Show |
SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr6 | 33445819 | ||||||
| chr6:33445819 | CTTTTTTT | C | 6 | a0001c0001t0001g0021 a0001c0001t0001g0031 a0001c0001t0001g0075 others(3): Show |
9 | HG00544.hp2 HG00741.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.3583-740_3583-734d others(9): Show |
SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr6 | 33445819 | ||||||
| chr6:33445823 | T | C | 3 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0010g0167 |
3 | HG02647.hp1 HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3583-752T>C | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 16/18 | chr6 | 33445823 | |||||||
| chr6:33445825 | T | C | 1 | a0001c0001t0001g0100 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3583-750T>C | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 16/18 | chr6 | 33445825 | |||||||
| chr6:33446211 | G | C | 1 | a0001c0001t0010g0167 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3583-364G>C | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 16/18 | chr6 | 33446211 | |||||||
| chr6:33446424 | A | G | 2 | a0001c0001t0001g0176 a0001c0001t0001g0177 |
2 | HG00642.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.3583-151A>G | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 16/18 | chr6 | 33446424 | |||||||
| chr6:33446516 | G | A | 1 | a0001c0002t0001g0132 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3583-59G>A | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 16/18 | chr6 | 33446516 | |||||||
| chr6:33446849 | T | C | 187 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(184): Show |
299 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.3794+63T>C | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 17/18 | chr6 | 33446849 | |||||||
| chr6:33446860 | G | T | 187 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(184): Show |
299 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.3794+74G>T | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 17/18 | chr6 | 33446860 | |||||||
| chr6:33446958 | C | T | 1 | a0002c0006t0001g0175 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.3794+172C>T | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 17/18 | chr6 | 33446958 | |||||||
| chr6:33446962 | A | G | 1 | a0001c0001t0001g0089 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3794+176A>G | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 17/18 | chr6 | 33446962 | |||||||
| chr6:33447182 | T | G | 1 | a0001c0003t0001g0110 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3794+396T>G | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 17/18 | chr6 | 33447182 | |||||||
| chr6:33447215 | T | C | 1 | a0001c0001t0001g0090 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.3794+429T>C | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 17/18 | chr6 | 33447215 | |||||||
| chr6:33447530 | C | G | 61 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(58): Show |
99 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.3795-313C>G | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 17/18 | chr6 | 33447530 | |||||||
| chr6:33448090 | C | G | 4 | a0001c0007t0001g0038 a0001c0007t0001g0113 a0001c0007t0001g0114 others(1): Show |
5 | HG02630.hp1 HG03139.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.3885+157C>G | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 18/18 | chr6 | 33448090 | |||||||
| chr6:33448177 | C | T | 1 | a0001c0002t0001g0149 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.3885+244C>T | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 18/18 | chr6 | 33448177 | |||||||
| chr6:33448305 | C | T | 1 | a0001c0001t0002g0085 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3885+372C>T | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 18/18 | chr6 | 33448305 | |||||||
| chr6:33448334 | C | T | 75 | a0001c0001t0001g0016 a0001c0001t0001g0041 a0001c0001t0001g0123 others(72): Show |
131 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.3885+401C>T | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 18/18 | chr6 | 33448334 | |||||||
| chr6:33448346 | T | G | 5 | a0001c0004t0001g0015 a0001c0004t0001g0159 a0001c0004t0001g0160 others(2): Show |
8 | HG02145.hp2 HG02257.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.3885+413T>G | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 18/18 | chr6 | 33448346 | |||||||
| chr6:33448477 | C | CAAG | 3 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 |
3 | HG02818.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.3885+544_3885+545i others(5): Show |
SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 18/18 | chr6 | 33448477 | |||||||
| chr6:33448478 | T | A | 3 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 |
3 | HG02818.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.3885+545T>A | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 18/18 | chr6 | 33448478 | |||||||
| chr6:33448572 | C | G | 1 | a0001c0004t0001g0159 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3885+639C>G | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 18/18 | chr6 | 33448572 | |||||||
| chr6:33448594 | G | A | 1 | a0001c0002t0001g0146 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.3885+661G>A | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 18/18 | chr6 | 33448594 | |||||||
| chr6:33448731 | G | A | 6 | a0001c0001t0001g0021 a0001c0001t0001g0117 a0001c0001t0001g0176 others(3): Show |
8 | HG00642.hp2 HG00741.hp1 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.3885+798G>A | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 18/18 | chr6 | 33448731 | |||||||
| chr6:33448966 | C | T | 1 | a0001c0002t0001g0146 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.3885+1033C>T | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 18/18 | chr6 | 33448966 | |||||||
| chr6:33449041 | C | T | 10 | a0001c0003t0001g0004 a0001c0003t0001g0029 a0001c0003t0001g0030 others(7): Show |
17 | HG01884.hp1 HG01891.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.3885+1108C>T | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 18/18 | chr6 | 33449041 | |||||||
| chr6:33449127 | C | T | 2 | a0001c0001t0001g0139 a0001c0002t0001g0178 |
2 | HG01255.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.3885+1194C>T | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 18/18 | chr6 | 33449127 | |||||||
| chr6:33449345 | C | T | 10 | a0001c0001t0001g0016 a0001c0004t0001g0015 a0001c0004t0001g0044 others(7): Show |
18 | HG01123.hp1 HG02055.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.3885+1412C>T | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 18/18 | chr6 | 33449345 | |||||||
| chr6:33449496 | T | C | 1 | a0001c0002t0001g0156 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.3885+1563T>C | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 18/18 | chr6 | 33449496 | |||||||
| chr6:33450000 | T | G | 9 | a0001c0004t0001g0015 a0001c0004t0001g0044 a0001c0004t0001g0045 others(6): Show |
14 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.3886-1760T>G | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 18/18 | chr6 | 33450000 | |||||||
| chr6:33450031 | T | C | 1 | a0001c0002t0001g0133 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.3886-1729T>C | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 18/18 | chr6 | 33450031 | |||||||
| chr6:33450527 | C | T | 1 | a0001c0002t0001g0145 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.3886-1233C>T | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 18/18 | chr6 | 33450527 | |||||||
| chr6:33450584 | G | A | 2 | a0001c0001t0001g0021 a0001c0001t0001g0117 |
4 | HG00741.hp1 HG02622.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.3886-1176G>A | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 18/18 | chr6 | 33450584 | |||||||
| chr6:33450696 | A | G | 15 | a0001c0001t0001g0028 a0001c0001t0001g0063 a0001c0001t0001g0064 others(12): Show |
18 | HG00639.hp1 HG00642.hp1 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.3886-1064A>G | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 18/18 | chr6 | 33450696 | |||||||
| chr6:33450697 | T | C | 1 | a0001c0001t0001g0080 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.3886-1063T>C | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 18/18 | chr6 | 33450697 | |||||||
| chr6:33450903 | C | T | 5 | a0001c0001t0001g0010 a0001c0001t0001g0035 a0001c0001t0001g0101 others(2): Show |
9 | HG01192.hp2 HG01243.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.3886-857C>T | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 18/18 | chr6 | 33450903 | |||||||
| chr6:33451029 | G | A | 1 | a0001c0007t0001g0066 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3886-731G>A | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 18/18 | chr6 | 33451029 | |||||||
| chr6:33451187 | C | T | 1 | a0001c0005t0001g0055 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.3886-573C>T | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 18/18 | chr6 | 33451187 | |||||||
| chr6:33451194 | A | C | 1 | a0001c0001t0001g0096 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.3886-566A>C | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 18/18 | chr6 | 33451194 | |||||||
| chr6:33451286 | C | T | 1 | a0001c0013t0001g0072 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3886-474C>T | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 18/18 | chr6 | 33451286 | |||||||
| chr6:33451445 | G | T | 1 | a0001c0002t0013g0144 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.3886-315G>T | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 18/18 | chr6 | 33451445 | |||||||
| chr6:33451638 | G | A | 1 | a0001c0001t0010g0167 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3886-122G>A | SYNGAP1 | ENSG00000197283.18 | transcript | ENST00000646630.1 | protein_coding | 18/18 | chr6 | 33451638 |