Item | Value |
---|---|
geneid | 23198 |
ensemblid | ENSG00000068878.15 |
hgncid | 20635 |
symbol | PSME4 |
name | proteasome activator subunit 4 |
refseq_nuc | NM_014614.3 |
refseq_prot | NP_055429.2 |
ensembl_nuc | ENST00000404125.6 |
ensembl_prot | ENSP00000384211.1 |
mane_status | MANE Select |
chr | chr2 |
start | 53864069 |
end | 53970993 |
strand | - |
ver | v1.2 |
region | chr2:53864069-53970993 |
region5000 | chr2:53859069-53975993 |
regionname0 | PSME4_chr2_53864069_53970993 |
regionname5000 | PSME4_chr2_53859069_53975993 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 1843 | 172 | 63 | 32 | 47 | 11 | 18 | 34 | PSME4_chr2_53859069_53975993 | PSME4 | MEPAE others(1838): Show |
chr2 | 53859069 | 53975993 |
a0002 | 0/1 | 1843 | 130 | 15 | 18 | 72 | 3 | 21 | 55 | PSME4_chr2_53859069_53975993 | PSME4 | MEPAE others(1838): Show |
chr2 | 53859069 | 53975993 |
a0003 | 0/0 | 1843 | 57 | 6 | 4 | 47 | 0 | 0 | 39 | PSME4_chr2_53859069_53975993 | PSME4 | MEPAE others(1838): Show |
chr2 | 53859069 | 53975993 |
a0004 | 0/0 | 1843 | 8 | 0 | 6 | 1 | 0 | 1 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | MEPAE others(1838): Show |
chr2 | 53859069 | 53975993 |
a0005 | 0/0 | 1843 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | MEPAE others(1838): Show |
chr2 | 53859069 | 53975993 |
a0006 | 0/0 | 1843 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | MEPAE others(1838): Show |
chr2 | 53859069 | 53975993 |
a0007 | 0/0 | 1843 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | PSME4_chr2_53859069_53975993 | PSME4 | MEPAE others(1838): Show |
chr2 | 53859069 | 53975993 |
a0008 | 0/0 | 1843 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | MEPAE others(1838): Show |
chr2 | 53859069 | 53975993 |
a0009 | 0/0 | 1843 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | MEPAE others(1838): Show |
chr2 | 53859069 | 53975993 |
a0010 | 0/0 | 1843 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | MEPAE others(1838): Show |
chr2 | 53859069 | 53975993 |
a0011 | 0/0 | 1843 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | MEPAE others(1838): Show |
chr2 | 53859069 | 53975993 |
a0012 | 0/0 | 1843 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | MEPAE others(1838): Show |
chr2 | 53859069 | 53975993 |
a0013 | 0/0 | 1843 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | MEPAE others(1838): Show |
chr2 | 53859069 | 53975993 |
a0014 | 0/0 | 1843 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | MEPAE others(1838): Show |
chr2 | 53859069 | 53975993 |
a0015 | 0/0 | 1843 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | MEPAE others(1838): Show |
chr2 | 53859069 | 53975993 |
a0016 | 0/0 | 1843 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | MEPAE others(1838): Show |
chr2 | 53859069 | 53975993 |
a0017 | 0/0 | 1843 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | MEPAE others(1838): Show |
chr2 | 53859069 | 53975993 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 5529 | 72 | 26 | 19 | 7 | 6 | 13 | PSME4_chr2_53859069_53975993 | PSME4 | ATGGA others(5524): Show |
chr2 | 53859069 | 53975993 | ||
a0001c0005 | 0/0 | 5529 | 46 | 1 | 4 | 37 | 2 | 2 | PSME4_chr2_53859069_53975993 | PSME4 | ATGGA others(5524): Show |
chr2 | 53859069 | 53975993 | ||
a0001c0006 | 0/0 | 5529 | 35 | 23 | 5 | 3 | 3 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | ATGGA others(5524): Show |
chr2 | 53859069 | 53975993 | ||
a0001c0007 | 0/0 | 5529 | 8 | 6 | 1 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | ATGGA others(5524): Show |
chr2 | 53859069 | 53975993 | ||
a0001c0009 | 0/0 | 5529 | 7 | 6 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | ATGGA others(5524): Show |
chr2 | 53859069 | 53975993 | ||
a0001c0017 | 0/0 | 5529 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | ATGGA others(5524): Show |
chr2 | 53859069 | 53975993 | ||
a0001c0018 | 0/0 | 5529 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | ATGGA others(5524): Show |
chr2 | 53859069 | 53975993 | ||
a0001c0019 | 0/0 | 5529 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | ATGGA others(5524): Show |
chr2 | 53859069 | 53975993 | ||
a0001c0022 | 0/0 | 5529 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | ATGGA others(5524): Show |
chr2 | 53859069 | 53975993 | ||
a0002c0002 | 0/0 | 5529 | 62 | 6 | 0 | 46 | 2 | 8 | PSME4_chr2_53859069_53975993 | PSME4 | ATGGA others(5524): Show |
chr2 | 53859069 | 53975993 | ||
a0002c0003 | 0/1 | 5529 | 59 | 6 | 16 | 24 | 1 | 11 | PSME4_chr2_53859069_53975993 | PSME4 | ATGGA others(5524): Show |
chr2 | 53859069 | 53975993 | ||
a0002c0010 | 0/0 | 5529 | 3 | 3 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | ATGGA others(5524): Show |
chr2 | 53859069 | 53975993 | ||
a0002c0015 | 0/0 | 5529 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | ATGGA others(5524): Show |
chr2 | 53859069 | 53975993 | ||
a0002c0020 | 0/0 | 5529 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | ATGGA others(5524): Show |
chr2 | 53859069 | 53975993 | ||
a0002c0021 | 0/0 | 5529 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | ATGGA others(5524): Show |
chr2 | 53859069 | 53975993 | ||
a0002c0029 | 0/0 | 5529 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | ATGGA others(5524): Show |
chr2 | 53859069 | 53975993 | ||
a0002c0032 | 0/0 | 5529 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | ATGGA others(5524): Show |
chr2 | 53859069 | 53975993 | ||
a0002c0033 | 0/0 | 5529 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | ATGGA others(5524): Show |
chr2 | 53859069 | 53975993 | ||
a0003c0004 | 0/0 | 5529 | 57 | 6 | 4 | 47 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | ATGGA others(5524): Show |
chr2 | 53859069 | 53975993 | ||
a0004c0008 | 0/0 | 5529 | 8 | 0 | 6 | 1 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | ATGGA others(5524): Show |
chr2 | 53859069 | 53975993 | ||
a0005c0011 | 0/0 | 5529 | 3 | 2 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | ATGGA others(5524): Show |
chr2 | 53859069 | 53975993 | ||
a0006c0012 | 0/0 | 5529 | 2 | 2 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | ATGGA others(5524): Show |
chr2 | 53859069 | 53975993 | ||
a0007c0013 | 0/0 | 5529 | 2 | 0 | 0 | 2 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | ATGGA others(5524): Show |
chr2 | 53859069 | 53975993 | ||
a0008c0025 | 0/0 | 5529 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | ATGGA others(5524): Show |
chr2 | 53859069 | 53975993 | ||
a0009c0031 | 0/0 | 5529 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | ATGGA others(5524): Show |
chr2 | 53859069 | 53975993 | ||
a0010c0027 | 0/0 | 5529 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | ATGGA others(5524): Show |
chr2 | 53859069 | 53975993 | ||
a0011c0016 | 0/0 | 5529 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | ATGGA others(5524): Show |
chr2 | 53859069 | 53975993 | ||
a0012c0023 | 0/0 | 5529 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | ATGGA others(5524): Show |
chr2 | 53859069 | 53975993 | ||
a0013c0030 | 0/0 | 5529 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | ATGGA others(5524): Show |
chr2 | 53859069 | 53975993 | ||
a0014c0026 | 0/0 | 5529 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | ATGGA others(5524): Show |
chr2 | 53859069 | 53975993 | ||
a0015c0028 | 0/0 | 5529 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | ATGGA others(5524): Show |
chr2 | 53859069 | 53975993 | ||
a0016c0024 | 0/0 | 5529 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | ATGGA others(5524): Show |
chr2 | 53859069 | 53975993 | ||
a0017c0014 | 0/0 | 5529 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | ATGGA others(5524): Show |
chr2 | 53859069 | 53975993 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 7250 | 69 | 24 | 19 | 6 | 6 | 13 | PSME4_chr2_53859069_53975993 | PSME4 | AGAGC others(7245): Show |
chr2 | 53859069 | 53975993 |
a0001c0001t0003 | 0/0 | 7250 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | AGAGC others(7245): Show |
chr2 | 53859069 | 53975993 |
a0001c0001t0007 | 0/0 | 7251 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | AGAGC others(7246): Show |
chr2 | 53859069 | 53975993 |
a0001c0001t0012 | 0/0 | 7249 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | AGAGC others(7244): Show |
chr2 | 53859069 | 53975993 |
a0001c0005t0001 | 0/0 | 7250 | 43 | 1 | 4 | 34 | 2 | 2 | PSME4_chr2_53859069_53975993 | PSME4 | AGAGC others(7245): Show |
chr2 | 53859069 | 53975993 |
a0001c0005t0007 | 0/0 | 7251 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | AGAGC others(7246): Show |
chr2 | 53859069 | 53975993 |
a0001c0005t0009 | 0/0 | 7250 | 2 | 0 | 0 | 2 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | AGAGC others(7245): Show |
chr2 | 53859069 | 53975993 |
a0001c0006t0003 | 0/0 | 7250 | 29 | 18 | 5 | 3 | 2 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | AGAGC others(7245): Show |
chr2 | 53859069 | 53975993 |
a0001c0006t0005 | 0/0 | 7250 | 4 | 4 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | AGAGC others(7245): Show |
chr2 | 53859069 | 53975993 |
a0001c0006t0014 | 0/0 | 7250 | 1 | 0 | 0 | 0 | 1 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | AGAGC others(7245): Show |
chr2 | 53859069 | 53975993 |
a0001c0006t0015 | 0/0 | 7251 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | AGAGC others(7246): Show |
chr2 | 53859069 | 53975993 |
a0001c0007t0001 | 0/0 | 7250 | 4 | 2 | 1 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | AGAGC others(7245): Show |
chr2 | 53859069 | 53975993 |
a0001c0007t0006 | 0/0 | 7249 | 4 | 4 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | AGAGC others(7244): Show |
chr2 | 53859069 | 53975993 |
a0001c0009t0001 | 0/0 | 7250 | 6 | 5 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | AGAGC others(7245): Show |
chr2 | 53859069 | 53975993 |
a0001c0009t0013 | 0/0 | 7250 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | AGAGC others(7245): Show |
chr2 | 53859069 | 53975993 |
a0001c0017t0001 | 0/0 | 7250 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | AGAGC others(7245): Show |
chr2 | 53859069 | 53975993 |
a0001c0018t0001 | 0/0 | 7250 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | AGAGC others(7245): Show |
chr2 | 53859069 | 53975993 |
a0001c0019t0001 | 0/0 | 7250 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | AGAGC others(7245): Show |
chr2 | 53859069 | 53975993 |
a0001c0022t0016 | 0/0 | 7249 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | AGAGC others(7244): Show |
chr2 | 53859069 | 53975993 |
a0002c0002t0001 | 0/0 | 7250 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | AGAGC others(7245): Show |
chr2 | 53859069 | 53975993 |
a0002c0002t0002 | 0/0 | 7248 | 56 | 6 | 0 | 41 | 2 | 7 | PSME4_chr2_53859069_53975993 | PSME4 | AGAGC others(7243): Show |
chr2 | 53859069 | 53975993 |
a0002c0002t0004 | 0/0 | 7249 | 5 | 0 | 0 | 5 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | AGAGC others(7244): Show |
chr2 | 53859069 | 53975993 |
a0002c0003t0001 | 0/0 | 7250 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | AGAGC others(7245): Show |
chr2 | 53859069 | 53975993 |
a0002c0003t0002 | 0/1 | 7248 | 53 | 5 | 16 | 21 | 1 | 9 | PSME4_chr2_53859069_53975993 | PSME4 | AGAGC others(7243): Show |
chr2 | 53859069 | 53975993 |
a0002c0003t0004 | 0/0 | 7249 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | AGAGC others(7244): Show |
chr2 | 53859069 | 53975993 |
a0002c0003t0008 | 0/0 | 7248 | 2 | 0 | 0 | 2 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | AGAGC others(7243): Show |
chr2 | 53859069 | 53975993 |
a0002c0003t0010 | 0/0 | 7248 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | AGAGC others(7243): Show |
chr2 | 53859069 | 53975993 |
a0002c0003t0011 | 0/0 | 7248 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | AGAGC others(7243): Show |
chr2 | 53859069 | 53975993 |
a0002c0010t0002 | 0/0 | 7248 | 3 | 3 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | AGAGC others(7243): Show |
chr2 | 53859069 | 53975993 |
a0002c0015t0002 | 0/0 | 7248 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | AGAGC others(7243): Show |
chr2 | 53859069 | 53975993 |
a0002c0020t0002 | 0/0 | 7248 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | AGAGC others(7243): Show |
chr2 | 53859069 | 53975993 |
a0002c0021t0002 | 0/0 | 7248 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | AGAGC others(7243): Show |
chr2 | 53859069 | 53975993 |
a0002c0029t0002 | 0/0 | 7248 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | AGAGC others(7243): Show |
chr2 | 53859069 | 53975993 |
a0002c0032t0004 | 0/0 | 7249 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | AGAGC others(7244): Show |
chr2 | 53859069 | 53975993 |
a0002c0033t0002 | 0/0 | 7248 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | AGAGC others(7243): Show |
chr2 | 53859069 | 53975993 |
a0003c0004t0001 | 0/0 | 7250 | 55 | 6 | 3 | 46 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | AGAGC others(7245): Show |
chr2 | 53859069 | 53975993 |
a0003c0004t0003 | 0/0 | 7250 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | AGAGC others(7245): Show |
chr2 | 53859069 | 53975993 |
a0003c0004t0007 | 0/0 | 7251 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | AGAGC others(7246): Show |
chr2 | 53859069 | 53975993 |
a0004c0008t0001 | 0/0 | 7250 | 8 | 0 | 6 | 1 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | AGAGC others(7245): Show |
chr2 | 53859069 | 53975993 |
a0005c0011t0001 | 0/0 | 7250 | 2 | 2 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | AGAGC others(7245): Show |
chr2 | 53859069 | 53975993 |
a0005c0011t0002 | 0/0 | 7248 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | AGAGC others(7243): Show |
chr2 | 53859069 | 53975993 |
a0006c0012t0002 | 0/0 | 7248 | 2 | 2 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | AGAGC others(7243): Show |
chr2 | 53859069 | 53975993 |
a0007c0013t0002 | 0/0 | 7248 | 2 | 0 | 0 | 2 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | AGAGC others(7243): Show |
chr2 | 53859069 | 53975993 |
a0008c0025t0001 | 0/0 | 7250 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | AGAGC others(7245): Show |
chr2 | 53859069 | 53975993 |
a0009c0031t0002 | 0/0 | 7248 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | AGAGC others(7243): Show |
chr2 | 53859069 | 53975993 |
a0010c0027t0003 | 0/0 | 7250 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | AGAGC others(7245): Show |
chr2 | 53859069 | 53975993 |
a0011c0016t0001 | 0/0 | 7250 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | AGAGC others(7245): Show |
chr2 | 53859069 | 53975993 |
a0012c0023t0003 | 0/0 | 7250 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | AGAGC others(7245): Show |
chr2 | 53859069 | 53975993 |
a0013c0030t0002 | 0/0 | 7248 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | AGAGC others(7243): Show |
chr2 | 53859069 | 53975993 |
a0014c0026t0001 | 0/0 | 7250 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | AGAGC others(7245): Show |
chr2 | 53859069 | 53975993 |
a0015c0028t0001 | 0/0 | 7250 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | AGAGC others(7245): Show |
chr2 | 53859069 | 53975993 |
a0016c0024t0001 | 0/0 | 7250 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | AGAGC others(7245): Show |
chr2 | 53859069 | 53975993 |
a0017c0014t0002 | 0/0 | 7248 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | AGAGC others(7243): Show |
chr2 | 53859069 | 53975993 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0001t0001g0243 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0001t0003g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0001t0007g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0001t0012g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0005t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0005t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0005t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0005t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0005t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0005t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0005t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0005t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0005t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0005t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0005t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0005t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0005t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0005t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0005t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0005t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0005t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0005t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0005t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0005t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0005t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0005t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0005t0001g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0005t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0005t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0005t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0005t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0005t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0005t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0005t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0005t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0005t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0005t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0005t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0005t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0005t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0005t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0005t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0005t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0005t0001g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0005t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0005t0001g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0005t0001g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0005t0007g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0005t0009g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0005t0009g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0006t0003g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0006t0003g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0006t0003g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0006t0003g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0006t0003g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0006t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0006t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0006t0003g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0006t0003g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0006t0003g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0006t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0006t0003g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0006t0003g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0006t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0006t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0006t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0006t0003g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0006t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0006t0003g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0006t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0006t0003g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0006t0003g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0006t0003g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0006t0003g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0006t0003g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0006t0003g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0006t0003g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0006t0003g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0006t0003g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0006t0005g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0006t0005g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0006t0005g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0006t0005g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0006t0014g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0006t0015g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0007t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0007t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0007t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0007t0001g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0007t0006g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0007t0006g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0007t0006g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0007t0006g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0009t0001g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0009t0001g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0009t0001g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0009t0001g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0009t0001g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0009t0001g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0009t0013g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0017t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0018t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0019t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0001c0022t0016g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0002t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0002t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0002t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0002t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0002t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0002t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0002t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0002t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0002t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0002t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0002t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0002t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0002t0002g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0002t0002g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0002t0002g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0002t0002g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0002t0004g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0002t0004g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0002t0004g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0002t0004g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0002t0004g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0003t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0003t0002g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0003t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0003t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0003t0002g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0003t0002g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0003t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0003t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0003t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0003t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0003t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0003t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0003t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0003t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0003t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0003t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0003t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0003t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0003t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0003t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0003t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0003t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0003t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0003t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0003t0002g0101 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0003t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0003t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0003t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0003t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0003t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0003t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0003t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0003t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0003t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0003t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0003t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0003t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0003t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0003t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0003t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0003t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0003t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0003t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0003t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0003t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0003t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0003t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0003t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0003t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0003t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0003t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0003t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0003t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0003t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0003t0004g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0003t0008g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0003t0008g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0003t0010g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0003t0011g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0010t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0010t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0010t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0015t0002g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0020t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0021t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0029t0002g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0032t0004g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0002c0033t0002g0375 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0003c0004t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0003c0004t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0003c0004t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0003c0004t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0003c0004t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0003c0004t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0003c0004t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0003c0004t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0003c0004t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0003c0004t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0003c0004t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0003c0004t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0003c0004t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0003c0004t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0003c0004t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0003c0004t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0003c0004t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0003c0004t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0003c0004t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0003c0004t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0003c0004t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0003c0004t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0003c0004t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0003c0004t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0003c0004t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0003c0004t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0003c0004t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0003c0004t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0003c0004t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0003c0004t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0003c0004t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0003c0004t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0003c0004t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0003c0004t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0003c0004t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0003c0004t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0003c0004t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0003c0004t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0003c0004t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0003c0004t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0003c0004t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0003c0004t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0003c0004t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0003c0004t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0003c0004t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0003c0004t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0003c0004t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0003c0004t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0003c0004t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0003c0004t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0003c0004t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0003c0004t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0003c0004t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0003c0004t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0003c0004t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0003c0004t0003g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0003c0004t0007g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0004c0008t0001g0376 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0004c0008t0001g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0004c0008t0001g0378 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0004c0008t0001g0379 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0004c0008t0001g0380 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0004c0008t0001g0381 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0004c0008t0001g0382 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0004c0008t0001g0383 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0005c0011t0001g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0005c0011t0001g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0005c0011t0002g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0006c0012t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0006c0012t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0007c0013t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0007c0013t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0008c0025t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0009c0031t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0010c0027t0003g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0011c0016t0001g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0012c0023t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0013c0030t0002g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0014c0026t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0015c0028t0001g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0016c0024t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
a0017c0014t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0295 | EUR | GBR | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG00099 | hp2 | a0001 | c0006 | t0014 | g0164 | EUR | GBR | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0237 | EUR | FIN | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG00280 | hp2 | a0002 | c0002 | t0002 | g0083 | EUR | FIN | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG00323 | hp1 | a0002 | c0002 | t0002 | g0081 | EUR | FIN | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0273 | EUR | FIN | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG00408 | hp1 | a0001 | c0005 | t0001 | g0373 | EAS | CHS | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG00408 | hp2 | a0002 | c0003 | t0002 | g0110 | EAS | CHS | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG00423 | hp1 | a0001 | c0005 | t0001 | g0348 | EAS | CHS | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG00423 | hp2 | a0002 | c0002 | t0002 | g0093 | EAS | CHS | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG00438 | hp1 | a0002 | c0003 | t0002 | g0132 | EAS | CHS | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG00438 | hp2 | a0003 | c0004 | t0001 | g0289 | EAS | CHS | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG00544 | hp1 | a0002 | c0002 | t0002 | g0124 | EAS | CHS | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG00544 | hp2 | a0003 | c0004 | t0001 | g0251 | EAS | CHS | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG00558 | hp1 | a0002 | c0003 | t0002 | g0075 | EAS | CHS | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG00558 | hp2 | a0003 | c0004 | t0001 | g0183 | EAS | CHS | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG00597 | hp1 | a0001 | c0005 | t0001 | g0326 | EAS | CHS | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | CHS | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG00609 | hp1 | a0001 | c0005 | t0001 | g0349 | EAS | CHS | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | CHS | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG00621 | hp1 | a0001 | c0005 | t0007 | g0331 | EAS | CHS | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG00621 | hp2 | a0002 | c0002 | t0004 | g0118 | EAS | CHS | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG00733 | hp2 | a0002 | c0003 | t0002 | g0145 | AMR | PUR | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG00735 | hp1 | a0002 | c0003 | t0002 | g0105 | AMR | PUR | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG00735 | hp2 | a0003 | c0004 | t0001 | g0290 | AMR | PUR | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG00738 | hp2 | a0001 | c0006 | t0003 | g0161 | AMR | PUR | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG01069 | hp1 | a0001 | c0022 | t0016 | g0111 | AMR | PUR | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG01069 | hp2 | a0002 | c0003 | t0002 | g0134 | AMR | PUR | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG01070 | hp2 | a0004 | c0008 | t0001 | g0378 | AMR | PUR | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | PUR | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG01071 | hp2 | a0002 | c0003 | t0002 | g0135 | AMR | PUR | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG01074 | hp1 | a0001 | c0009 | t0001 | g0370 | AMR | PUR | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG01074 | hp2 | a0008 | c0025 | t0001 | g0259 | AMR | PUR | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0293 | AMR | PUR | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG01081 | hp2 | a0001 | c0007 | t0001 | g0015 | AMR | PUR | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0294 | AMR | PUR | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG01099 | hp2 | a0001 | c0006 | t0003 | g0027 | AMR | PUR | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG01106 | hp1 | a0001 | c0006 | t0003 | g0030 | AMR | PUR | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG01106 | hp2 | a0002 | c0003 | t0002 | g0108 | AMR | PUR | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG01109 | hp1 | a0003 | c0004 | t0003 | g0218 | AMR | PUR | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG01109 | hp2 | a0004 | c0008 | t0001 | g0381 | AMR | PUR | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG01167 | hp1 | a0002 | c0003 | t0002 | g0138 | AMR | PUR | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG01167 | hp2 | a0001 | c0006 | t0003 | g0156 | AMR | PUR | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG01168 | hp2 | a0002 | c0003 | t0002 | g0146 | AMR | PUR | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG01169 | hp2 | a0002 | c0003 | t0002 | g0147 | AMR | PUR | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG01175 | hp1 | a0002 | c0003 | t0002 | g0133 | AMR | PUR | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG01175 | hp2 | a0001 | c0005 | t0001 | g0313 | AMR | PUR | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0296 | AMR | PUR | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG01192 | hp2 | a0002 | c0003 | t0002 | g0020 | AMR | PUR | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG01243 | hp1 | a0005 | c0011 | t0002 | g0363 | AMR | PUR | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG01243 | hp2 | a0001 | c0005 | t0001 | g0182 | AMR | PUR | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG01255 | hp1 | a0002 | c0015 | t0002 | g0359 | AMR | CLM | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | CLM | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG01256 | hp1 | a0004 | c0008 | t0001 | g0380 | AMR | CLM | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG01256 | hp2 | a0002 | c0003 | t0002 | g0149 | AMR | CLM | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG01257 | hp1 | a0004 | c0008 | t0001 | g0382 | AMR | CLM | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG01257 | hp2 | a0002 | c0003 | t0002 | g0136 | AMR | CLM | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG01261 | hp1 | a0009 | c0031 | t0002 | g0021 | AMR | CLM | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0308 | AMR | CLM | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0278 | AMR | CLM | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG01346 | hp2 | a0001 | c0006 | t0003 | g0029 | AMR | CLM | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG01358 | hp1 | a0001 | c0005 | t0001 | g0315 | AMR | CLM | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | CLM | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | CLM | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | CLM | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | CLM | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG01496 | hp2 | a0001 | c0018 | t0001 | g0229 | AMR | CLM | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG01515 | hp1 | a0002 | c0003 | t0002 | g0152 | EUR | IBS | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG01515 | hp2 | a0001 | c0005 | t0001 | g0316 | EUR | IBS | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0189 | EUR | IBS | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG01516 | hp2 | a0001 | c0006 | t0003 | g0026 | EUR | IBS | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0036 | EUR | IBS | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG01517 | hp2 | a0001 | c0005 | t0001 | g0318 | EUR | IBS | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG01884 | hp1 | a0001 | c0006 | t0003 | g0266 | AFR | ACB | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG01884 | hp2 | a0003 | c0004 | t0001 | g0252 | AFR | ACB | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG01891 | hp1 | a0010 | c0027 | t0003 | g0162 | AFR | ACB | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG01891 | hp2 | a0005 | c0011 | t0001 | g0362 | AFR | ACB | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG01928 | hp1 | a0004 | c0008 | t0001 | g0379 | AMR | PEL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG01928 | hp2 | a0002 | c0003 | t0002 | g0148 | AMR | PEL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG01943 | hp1 | a0003 | c0004 | t0001 | g0258 | AMR | PEL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG01943 | hp2 | a0002 | c0021 | t0002 | g0113 | AMR | PEL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PEL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG01952 | hp2 | a0002 | c0003 | t0002 | g0112 | AMR | PEL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG01978 | hp1 | a0002 | c0003 | t0002 | g0139 | AMR | PEL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG01978 | hp2 | a0011 | c0016 | t0001 | g0339 | AMR | PEL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG02004 | hp1 | a0004 | c0008 | t0001 | g0376 | AMR | PEL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG02004 | hp2 | a0003 | c0004 | t0001 | g0260 | AMR | PEL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG02015 | hp1 | a0002 | c0002 | t0002 | g0355 | EAS | KHV | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG02015 | hp2 | a0003 | c0004 | t0001 | g0248 | EAS | KHV | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG02027 | hp1 | a0002 | c0002 | t0002 | g0117 | EAS | KHV | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG02027 | hp2 | a0003 | c0004 | t0001 | g0033 | EAS | KHV | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG02040 | hp1 | a0001 | c0005 | t0001 | g0372 | EAS | KHV | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG02040 | hp2 | a0002 | c0002 | t0002 | g0092 | EAS | KHV | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG02056 | hp1 | a0002 | c0002 | t0002 | g0143 | EAS | KHV | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG02056 | hp2 | a0001 | c0005 | t0001 | g0342 | EAS | KHV | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG02083 | hp1 | a0002 | c0002 | t0002 | g0084 | EAS | KHV | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG02083 | hp2 | a0002 | c0003 | t0002 | g0128 | EAS | KHV | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG02129 | hp1 | a0001 | c0005 | t0001 | g0329 | EAS | KHV | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG02129 | hp2 | a0002 | c0002 | t0002 | g0120 | EAS | KHV | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG02132 | hp1 | a0003 | c0004 | t0001 | g0300 | EAS | KHV | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG02132 | hp2 | a0001 | c0005 | t0001 | g0320 | EAS | KHV | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG02145 | hp1 | a0001 | c0006 | t0005 | g0004 | AFR | ACB | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | ACB | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG02155 | hp1 | a0002 | c0002 | t0002 | g0054 | EAS | CDX | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG02155 | hp2 | a0002 | c0003 | t0002 | g0066 | EAS | CDX | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | ACB | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG02257 | hp2 | a0001 | c0006 | t0003 | g0172 | AFR | ACB | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | ACB | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG02258 | hp2 | a0001 | c0006 | t0003 | g0217 | AFR | ACB | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG02280 | hp1 | a0003 | c0004 | t0001 | g0253 | AFR | ACB | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG02280 | hp2 | a0001 | c0006 | t0003 | g0175 | AFR | ACB | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG02293 | hp1 | a0001 | c0005 | t0001 | g0334 | AMR | PEL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PEL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG02451 | hp1 | a0001 | c0007 | t0001 | g0179 | AFR | ACB | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | ACB | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG02523 | hp1 | a0003 | c0004 | t0001 | g0256 | EAS | KHV | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG02523 | hp2 | a0002 | c0002 | t0004 | g0095 | EAS | KHV | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG02572 | hp1 | a0002 | c0010 | t0002 | g0018 | AFR | GWD | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG02572 | hp2 | a0003 | c0004 | t0001 | g0042 | AFR | GWD | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG02602 | hp1 | a0002 | c0003 | t0011 | g0009 | SAS | PJL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG02602 | hp2 | a0002 | c0002 | t0002 | g0086 | SAS | PJL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG02615 | hp1 | a0001 | c0006 | t0003 | g0176 | AFR | GWD | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG02615 | hp2 | a0002 | c0002 | t0002 | g0356 | AFR | GWD | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG02622 | hp1 | a0002 | c0002 | t0002 | g0087 | AFR | GWD | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG02622 | hp2 | a0003 | c0004 | t0001 | g0245 | AFR | GWD | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | GWD | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG02630 | hp2 | a0001 | c0006 | t0003 | g0171 | AFR | GWD | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG02647 | hp1 | a0003 | c0004 | t0001 | g0192 | AFR | GWD | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG02647 | hp2 | a0001 | c0006 | t0003 | g0371 | AFR | GWD | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG02683 | hp1 | a0001 | c0007 | t0001 | g0017 | SAS | PJL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG02683 | hp2 | a0001 | c0005 | t0001 | g0319 | SAS | PJL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0272 | SAS | PJL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG02698 | hp2 | a0002 | c0002 | t0002 | g0131 | SAS | PJL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG02717 | hp1 | a0001 | c0009 | t0001 | g0367 | AFR | GWD | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG02717 | hp2 | a0013 | c0030 | t0002 | g0310 | AFR | GWD | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG02735 | hp1 | a0004 | c0008 | t0001 | g0383 | SAS | PJL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG02735 | hp2 | a0002 | c0003 | t0002 | g0024 | SAS | PJL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG02738 | hp1 | a0001 | c0019 | t0001 | g0037 | SAS | PJL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG02809 | hp1 | a0002 | c0003 | t0010 | g0006 | AFR | GWD | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG02809 | hp2 | a0002 | c0002 | t0002 | g0357 | AFR | GWD | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG02818 | hp1 | a0001 | c0009 | t0001 | g0369 | AFR | GWD | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG02818 | hp2 | a0006 | c0012 | t0002 | g0062 | AFR | GWD | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG02886 | hp1 | a0001 | c0005 | t0001 | g0321 | AFR | GWD | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG02886 | hp2 | a0001 | c0006 | t0003 | g0157 | AFR | GWD | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG02895 | hp1 | a0001 | c0006 | t0003 | g0158 | AFR | GWD | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG02895 | hp2 | a0002 | c0002 | t0002 | g0121 | AFR | GWD | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG02896 | hp2 | a0001 | c0006 | t0003 | g0168 | AFR | GWD | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | GWD | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG02897 | hp2 | a0002 | c0002 | t0002 | g0088 | AFR | GWD | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG02922 | hp2 | a0002 | c0010 | t0002 | g0056 | AFR | ESN | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | ESN | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG02965 | hp2 | a0001 | c0007 | t0006 | g0196 | AFR | ESN | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG02970 | hp1 | a0002 | c0003 | t0002 | g0055 | AFR | ESN | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG02970 | hp2 | a0001 | c0006 | t0003 | g0031 | AFR | ESN | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | ESN | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG02976 | hp2 | a0001 | c0006 | t0005 | g0003 | AFR | ESN | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG03017 | hp2 | a0002 | c0029 | t0002 | g0307 | SAS | PJL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG03041 | hp2 | a0002 | c0003 | t0002 | g0049 | AFR | GWD | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG03098 | hp1 | a0014 | c0026 | t0001 | g0013 | AFR | MSL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG03098 | hp2 | a0001 | c0017 | t0001 | g0309 | AFR | MSL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | ESN | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG03130 | hp2 | a0006 | c0012 | t0002 | g0057 | AFR | ESN | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG03139 | hp1 | a0001 | c0009 | t0001 | g0366 | AFR | ESN | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG03139 | hp2 | a0001 | c0007 | t0001 | g0361 | AFR | ESN | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG03195 | hp1 | a0001 | c0006 | t0015 | g0169 | AFR | ESN | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG03195 | hp2 | a0002 | c0002 | t0002 | g0358 | AFR | ESN | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG03209 | hp1 | a0001 | c0007 | t0006 | g0197 | AFR | MSL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | MSL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | MSL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG03225 | hp2 | a0001 | c0007 | t0006 | g0014 | AFR | MSL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG03239 | hp1 | a0002 | c0003 | t0002 | g0060 | SAS | PJL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0209 | SAS | PJL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG03453 | hp1 | a0005 | c0011 | t0001 | g0364 | AFR | MSL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | MSL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG03486 | hp1 | a0001 | c0006 | t0003 | g0174 | AFR | MSL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | MSL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG03490 | hp1 | a0002 | c0003 | t0002 | g0078 | SAS | PJL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0224 | SAS | PJL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0227 | SAS | PJL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0244 | SAS | PJL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG03516 | hp1 | a0001 | c0001 | t0012 | g0041 | AFR | ESN | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG03516 | hp2 | a0001 | c0009 | t0001 | g0360 | AFR | ESN | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | GWD | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG03540 | hp2 | a0015 | c0028 | t0001 | g0368 | AFR | GWD | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG03579 | hp1 | a0016 | c0024 | t0001 | g0312 | AFR | MSL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG03579 | hp2 | a0002 | c0003 | t0002 | g0074 | AFR | MSL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0277 | SAS | PJL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG03669 | hp2 | a0002 | c0002 | t0002 | g0142 | SAS | PJL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG03704 | hp1 | a0001 | c0006 | t0003 | g0160 | SAS | PJL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0242 | SAS | PJL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG03710 | hp1 | a0002 | c0003 | t0002 | g0144 | SAS | PJL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG03710 | hp2 | a0002 | c0003 | t0002 | g0137 | SAS | PJL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG03831 | hp1 | a0001 | c0005 | t0001 | g0353 | SAS | BEB | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG03831 | hp2 | a0002 | c0002 | t0002 | g0154 | SAS | BEB | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG03834 | hp1 | a0002 | c0003 | t0002 | g0011 | SAS | BEB | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG03834 | hp2 | a0002 | c0002 | t0002 | g0153 | SAS | BEB | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG03927 | hp1 | a0002 | c0003 | t0002 | g0109 | SAS | BEB | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG03927 | hp2 | a0002 | c0002 | t0001 | g0235 | SAS | BEB | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG03942 | hp1 | a0002 | c0033 | t0002 | g0375 | SAS | BEB | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG03942 | hp2 | a0002 | c0003 | t0001 | g0079 | SAS | BEB | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG04115 | hp1 | a0002 | c0003 | t0002 | g0106 | SAS | STU | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | STU | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG04184 | hp1 | a0002 | c0002 | t0002 | g0151 | SAS | BEB | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0282 | SAS | BEB | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0281 | SAS | STU | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG04199 | hp2 | a0002 | c0003 | t0002 | g0127 | SAS | STU | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0276 | SAS | STU | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG04228 | hp2 | a0002 | c0002 | t0002 | g0141 | SAS | STU | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18522 | hp1 | a0001 | c0009 | t0001 | g0365 | AFR | YRI | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | YRI | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18612 | hp1 | a0002 | c0002 | t0002 | g0082 | EAS | CHB | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18612 | hp2 | a0001 | c0005 | t0001 | g0333 | EAS | CHB | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18747 | hp1 | a0001 | c0005 | t0001 | g0324 | EAS | CHB | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18747 | hp2 | a0003 | c0004 | t0001 | g0195 | EAS | CHB | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | YRI | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18906 | hp2 | a0001 | c0006 | t0003 | g0155 | AFR | YRI | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18940 | hp1 | a0001 | c0005 | t0001 | g0351 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18940 | hp2 | a0003 | c0004 | t0001 | g0291 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18941 | hp1 | a0002 | c0002 | t0002 | g0103 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18941 | hp2 | a0001 | c0005 | t0001 | g0323 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18943 | hp1 | a0001 | c0005 | t0001 | g0347 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18943 | hp2 | a0002 | c0003 | t0008 | g0008 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18945 | hp1 | a0003 | c0004 | t0001 | g0268 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18945 | hp2 | a0002 | c0002 | t0002 | g0050 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18948 | hp1 | a0002 | c0003 | t0002 | g0297 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18948 | hp2 | a0003 | c0004 | t0001 | g0202 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18950 | hp1 | a0001 | c0005 | t0001 | g0327 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18950 | hp2 | a0002 | c0003 | t0002 | g0299 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18951 | hp2 | a0001 | c0006 | t0003 | g0166 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18952 | hp1 | a0003 | c0004 | t0001 | g0201 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18952 | hp2 | a0002 | c0020 | t0002 | g0219 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18953 | hp1 | a0003 | c0004 | t0001 | g0285 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18953 | hp2 | a0001 | c0005 | t0001 | g0346 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18954 | hp1 | a0002 | c0002 | t0002 | g0063 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18954 | hp2 | a0004 | c0008 | t0001 | g0377 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18959 | hp1 | a0002 | c0002 | t0002 | g0043 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18959 | hp2 | a0003 | c0004 | t0001 | g0257 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18961 | hp1 | a0002 | c0002 | t0002 | g0129 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18961 | hp2 | a0001 | c0001 | t0007 | g0222 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18962 | hp1 | a0003 | c0004 | t0001 | g0246 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18962 | hp2 | a0002 | c0002 | t0002 | g0045 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18963 | hp1 | a0003 | c0004 | t0007 | g0288 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18963 | hp2 | a0001 | c0005 | t0001 | g0325 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18964 | hp1 | a0001 | c0005 | t0001 | g0330 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18964 | hp2 | a0003 | c0004 | t0001 | g0286 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18965 | hp1 | a0003 | c0004 | t0001 | g0039 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18965 | hp2 | a0002 | c0002 | t0002 | g0115 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18967 | hp1 | a0002 | c0003 | t0002 | g0019 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18967 | hp2 | a0003 | c0004 | t0001 | g0287 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18968 | hp1 | a0002 | c0002 | t0002 | g0102 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18968 | hp2 | a0001 | c0005 | t0009 | g0220 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18969 | hp1 | a0001 | c0005 | t0001 | g0317 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18969 | hp2 | a0003 | c0004 | t0001 | g0274 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18970 | hp1 | a0002 | c0003 | t0002 | g0071 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18970 | hp2 | a0002 | c0002 | t0002 | g0085 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18971 | hp1 | a0002 | c0002 | t0002 | g0065 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18971 | hp2 | a0001 | c0005 | t0009 | g0221 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18972 | hp1 | a0003 | c0004 | t0001 | g0200 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18972 | hp2 | a0002 | c0002 | t0002 | g0097 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18973 | hp1 | a0001 | c0006 | t0003 | g0163 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18973 | hp2 | a0003 | c0004 | t0001 | g0194 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18975 | hp1 | a0002 | c0002 | t0002 | g0122 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18975 | hp2 | a0001 | c0006 | t0003 | g0165 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18978 | hp1 | a0002 | c0002 | t0002 | g0044 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18978 | hp2 | a0003 | c0004 | t0001 | g0304 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18981 | hp1 | a0002 | c0003 | t0002 | g0114 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18981 | hp2 | a0003 | c0004 | t0001 | g0303 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18982 | hp1 | a0002 | c0003 | t0002 | g0076 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18982 | hp2 | a0002 | c0002 | t0002 | g0089 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18983 | hp1 | a0001 | c0005 | t0001 | g0343 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18983 | hp2 | a0003 | c0004 | t0001 | g0264 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18984 | hp1 | a0002 | c0003 | t0002 | g0070 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18984 | hp2 | a0002 | c0002 | t0002 | g0090 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18986 | hp1 | a0002 | c0002 | t0002 | g0068 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18986 | hp2 | a0001 | c0005 | t0001 | g0336 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18988 | hp1 | a0017 | c0014 | t0002 | g0067 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18989 | hp1 | a0003 | c0004 | t0001 | g0302 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18989 | hp2 | a0002 | c0002 | t0002 | g0125 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18990 | hp1 | a0002 | c0002 | t0002 | g0140 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18990 | hp2 | a0003 | c0004 | t0001 | g0247 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18991 | hp1 | a0002 | c0003 | t0002 | g0016 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18991 | hp2 | a0002 | c0032 | t0004 | g0374 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18994 | hp1 | a0003 | c0004 | t0001 | g0034 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18994 | hp2 | a0001 | c0005 | t0001 | g0345 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18995 | hp1 | a0003 | c0004 | t0001 | g0298 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18995 | hp2 | a0002 | c0003 | t0002 | g0072 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18999 | hp1 | a0003 | c0004 | t0001 | g0255 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18999 | hp2 | a0002 | c0002 | t0002 | g0116 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA19000 | hp1 | a0001 | c0005 | t0001 | g0311 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA19000 | hp2 | a0002 | c0003 | t0002 | g0104 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA19001 | hp1 | a0002 | c0002 | t0004 | g0048 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA19001 | hp2 | a0003 | c0004 | t0001 | g0040 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA19002 | hp1 | a0007 | c0013 | t0002 | g0046 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA19002 | hp2 | a0001 | c0005 | t0001 | g0341 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA19003 | hp2 | a0002 | c0003 | t0002 | g0080 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA19004 | hp1 | a0003 | c0004 | t0001 | g0265 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA19004 | hp2 | a0001 | c0005 | t0001 | g0328 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA19006 | hp1 | a0007 | c0013 | t0002 | g0073 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA19006 | hp2 | a0003 | c0004 | t0001 | g0306 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA19009 | hp1 | a0003 | c0004 | t0001 | g0262 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA19009 | hp2 | a0001 | c0005 | t0001 | g0332 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA19011 | hp1 | a0003 | c0004 | t0001 | g0301 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA19011 | hp2 | a0002 | c0002 | t0002 | g0126 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA19030 | hp1 | a0001 | c0006 | t0003 | g0167 | AFR | LWK | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | LWK | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA19043 | hp1 | a0002 | c0003 | t0002 | g0058 | AFR | LWK | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA19043 | hp2 | a0001 | c0006 | t0003 | g0177 | AFR | LWK | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA19055 | hp1 | a0002 | c0003 | t0004 | g0340 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA19055 | hp2 | a0002 | c0002 | t0002 | g0047 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA19056 | hp1 | a0003 | c0004 | t0001 | g0269 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA19056 | hp2 | a0002 | c0002 | t0002 | g0094 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA19057 | hp1 | a0003 | c0004 | t0001 | g0249 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA19057 | hp2 | a0001 | c0005 | t0001 | g0335 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA19058 | hp1 | a0002 | c0002 | t0002 | g0023 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA19058 | hp2 | a0003 | c0004 | t0001 | g0283 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA19062 | hp1 | a0001 | c0005 | t0001 | g0354 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA19062 | hp2 | a0002 | c0002 | t0002 | g0119 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA19063 | hp1 | a0003 | c0004 | t0001 | g0263 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA19063 | hp2 | a0002 | c0002 | t0002 | g0096 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA19065 | hp1 | a0002 | c0002 | t0002 | g0091 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA19065 | hp2 | a0001 | c0005 | t0001 | g0337 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA19066 | hp1 | a0001 | c0005 | t0001 | g0344 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA19067 | hp1 | a0002 | c0003 | t0002 | g0107 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA19067 | hp2 | a0002 | c0002 | t0004 | g0123 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA19070 | hp1 | a0003 | c0004 | t0001 | g0261 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA19070 | hp2 | a0002 | c0003 | t0002 | g0052 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA19072 | hp1 | a0002 | c0002 | t0004 | g0064 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA19072 | hp2 | a0003 | c0004 | t0001 | g0271 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA19075 | hp1 | a0002 | c0002 | t0002 | g0099 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA19075 | hp2 | a0003 | c0004 | t0001 | g0207 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA19077 | hp1 | a0003 | c0004 | t0001 | g0193 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA19077 | hp2 | a0002 | c0002 | t0002 | g0100 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA19079 | hp1 | a0002 | c0002 | t0002 | g0022 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA19079 | hp2 | a0001 | c0005 | t0001 | g0352 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA19080 | hp1 | a0002 | c0002 | t0002 | g0130 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA19080 | hp2 | a0001 | c0005 | t0001 | g0322 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA19085 | hp1 | a0003 | c0004 | t0001 | g0206 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA19085 | hp2 | a0002 | c0003 | t0008 | g0007 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA19086 | hp1 | a0002 | c0003 | t0002 | g0069 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA19086 | hp2 | a0003 | c0004 | t0001 | g0284 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA19087 | hp1 | a0001 | c0005 | t0001 | g0314 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA19087 | hp2 | a0002 | c0002 | t0002 | g0098 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA19088 | hp1 | a0003 | c0004 | t0001 | g0250 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA19088 | hp2 | a0002 | c0003 | t0002 | g0059 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA19091 | hp1 | a0001 | c0005 | t0001 | g0338 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA19091 | hp2 | a0002 | c0003 | t0002 | g0061 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | YRI | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA19240 | hp2 | a0001 | c0006 | t0003 | g0159 | AFR | YRI | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | ASW | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA20129 | hp2 | a0001 | c0006 | t0005 | g0002 | AFR | ASW | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0208 | EUR | TSI | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA20805 | hp2 | a0001 | c0006 | t0003 | g0025 | EUR | TSI | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | CLM | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG01123 | hp2 | a0002 | c0003 | t0002 | g0150 | AMR | CLM | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG02109 | hp1 | a0001 | c0006 | t0005 | g0005 | AFR | ACB | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG02109 | hp2 | a0003 | c0004 | t0001 | g0254 | AFR | ACB | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG02486 | hp1 | a0012 | c0023 | t0003 | g0028 | AFR | ACB | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0279 | AFR | ACB | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG02559 | hp1 | a0001 | c0006 | t0003 | g0178 | AFR | ACB | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG02559 | hp2 | a0001 | c0007 | t0006 | g0012 | AFR | ACB | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG03471 | hp1 | a0001 | c0001 | t0003 | g0203 | AFR | MSL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG03471 | hp2 | a0002 | c0010 | t0002 | g0051 | AFR | MSL | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG06807 | hp1 | a0002 | c0003 | t0002 | g0077 | AFR | USA | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
HG06807 | hp2 | a0001 | c0006 | t0003 | g0170 | AFR | USA | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18955 | hp1 | a0003 | c0004 | t0001 | g0032 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA18955 | hp2 | a0001 | c0005 | t0001 | g0350 | EAS | JPT | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | USA | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
NA20300 | hp2 | a0001 | c0009 | t0013 | g0292 | AFR | USA | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
homoSapiens | chm13v2 | a0002 | c0003 | t0002 | g0101 | REF | REF | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0243 | REF | REF | PSME4_chr2_53859069_53975993 | PSME4 | chr2 | 53859069 | 53975993 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:53869391 | T | C | 1 | a0006 | 2 | HG02818.hp2 HG03130.hp2 |
missense_variant | MODERATE | c.5248A>G | p.Thr1750Ala | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/47 | 5457/7250 | 5248/5532 | 1750/1843 | chr2 | 53869391 | |||
chr2:53892888 | A | T | 7 | a0002 a0005 a0006 others(4): Show |
139 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(136): Show |
missense_variant | MODERATE | c.4111T>A | p.Ser1371Thr | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 36/47 | 4320/7250 | 4111/5532 | 1371/1843 | chr2 | 53892888 | |||
chr2:53904110 | T | A | 1 | a0007 | 2 | NA19002.hp1 NA19006.hp1 |
missense_variant | MODERATE | c.2990A>T | p.Tyr997Phe | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 27/47 | 3199/7250 | 2990/5532 | 997/1843 | chr2 | 53904110 | |||
chr2:53906849 | T | C | 1 | a0008 | 1 | HG01074.hp2 | missense_variant | MODERATE | c.2804A>G | p.His935Arg | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 25/47 | 3013/7250 | 2804/5532 | 935/1843 | chr2 | 53906849 | |||
chr2:53908331 | T | C | 1 | a0012 | 1 | HG02486.hp1 | missense_variant | MODERATE | c.2773A>G | p.Met925Val | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 24/47 | 2982/7250 | 2773/5532 | 925/1843 | chr2 | 53908331 | |||
chr2:53908553 | T | C | 1 | a0016 | 1 | HG03579.hp1 | missense_variant | MODERATE | c.2642A>G | p.Asp881Gly | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 23/47 | 2851/7250 | 2642/5532 | 881/1843 | chr2 | 53908553 | |||
chr2:53908799 | T | C | 2 | a0003 a0008 |
58 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(55): Show |
missense_variant | MODERATE | c.2614A>G | p.Ile872Val | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 22/47 | 2823/7250 | 2614/5532 | 872/1843 | chr2 | 53908799 | |||
chr2:53919155 | T | C | 1 | a0014 | 1 | HG03098.hp1 | missense_variant | MODERATE | c.2512A>G | p.Asn838Asp | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/47 | 2721/7250 | 2512/5532 | 838/1843 | chr2 | 53919155 | |||
chr2:53920941 | C | T | 1 | a0011 | 1 | HG01978.hp2 | missense_variant | MODERATE | c.2210G>A | p.Cys737Tyr | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 18/47 | 2419/7250 | 2210/5532 | 737/1843 | chr2 | 53920941 | |||
chr2:53920978 | G | A | 1 | a0010 | 1 | HG01891.hp1 | missense_variant | MODERATE | c.2173C>T | p.Leu725Phe | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 18/47 | 2382/7250 | 2173/5532 | 725/1843 | chr2 | 53920978 | |||
chr2:53931953 | T | C | 1 | a0015 | 1 | HG03540.hp2 | missense_variant | MODERATE | c.1198A>G | p.Ile400Val | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 10/47 | 1407/7250 | 1198/5532 | 400/1843 | chr2 | 53931953 | |||
chr2:53936137 | A | T | 1 | a0017 | 1 | NA18988.hp1 | missense_variant | MODERATE | c.784T>A | p.Leu262Met | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 7/47 | 993/7250 | 784/5532 | 262/1843 | chr2 | 53936137 | |||
chr2:53937391 | T | C | 2 | a0005 a0013 |
4 | HG01243.hp1 HG01891.hp2 HG02717.hp2 others(1): Show |
missense_variant&splice_region_variant | MODERATE | c.695A>G | p.Lys232Arg | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 5/47 | 904/7250 | 695/5532 | 232/1843 | chr2 | 53937391 | |||
chr2:53948527 | G | A | 1 | a0013 | 1 | HG02717.hp2 | missense_variant | MODERATE | c.394C>T | p.Leu132Phe | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/47 | 603/7250 | 394/5532 | 132/1843 | chr2 | 53948527 | |||
chr2:53949279 | T | C | 1 | a0009 | 1 | HG01261.hp1 | missense_variant | MODERATE | c.247A>G | p.Ile83Val | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 2/47 | 456/7250 | 247/5532 | 83/1843 | chr2 | 53949279 | |||
chr2:53970692 | C | A | 1 | a0004 | 8 | HG01070.hp2 HG01109.hp2 HG01256.hp1 others(5): Show |
missense_variant | MODERATE | c.93G>T | p.Glu31Asp | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/47 | 302/7250 | 93/5532 | 31/1843 | chr2 | 53970692 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:53866122 | G | A | 1 | a0002c0021 | 1 | HG01943.hp2 | synonymous_variant | LOW | c.5499C>T | p.Thr1833Thr | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 46/47 | 5708/7250 | 5499/5532 | 1833/1843 | chr2 | 53866122 | |||
chr2:53866819 | G | A | 3 | a0001c0006 a0010c0027 a0012c0023 |
37 | HG00099.hp2 HG00738.hp2 HG01099.hp2 others(34): Show |
synonymous_variant | LOW | c.5325C>T | p.Tyr1775Tyr | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 45/47 | 5534/7250 | 5325/5532 | 1775/1843 | chr2 | 53866819 | |||
chr2:53887962 | A | T | 1 | a0001c0019 | 1 | HG02738.hp1 | synonymous_variant | LOW | c.4416T>A | p.Leu1472Leu | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 39/47 | 4625/7250 | 4416/5532 | 1472/1843 | chr2 | 53887962 | |||
chr2:53888767 | A | G | 16 | a0001c0022 a0002c0002 a0002c0003 others(13): Show |
140 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(137): Show |
synonymous_variant | LOW | c.4342T>C | p.Leu1448Leu | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 38/47 | 4551/7250 | 4342/5532 | 1448/1843 | chr2 | 53888767 | |||
chr2:53893683 | G | A | 23 | a0001c0005 a0001c0006 a0001c0009 others(20): Show |
239 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(236): Show |
synonymous_variant | LOW | c.4029C>T | p.Cys1343Cys | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 35/47 | 4238/7250 | 4029/5532 | 1343/1843 | chr2 | 53893683 | |||
chr2:53898342 | A | G | 1 | a0002c0010 | 3 | HG02572.hp1 HG02922.hp2 HG03471.hp2 |
synonymous_variant | LOW | c.3435T>C | p.Asn1145Asn | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 30/47 | 3644/7250 | 3435/5532 | 1145/1843 | chr2 | 53898342 | |||
chr2:53899904 | C | T | 25 | a0001c0005 a0001c0006 a0001c0007 others(22): Show |
248 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(245): Show |
synonymous_variant | LOW | c.3399G>A | p.Gln1133Gln | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 29/47 | 3608/7250 | 3399/5532 | 1133/1843 | chr2 | 53899904 | |||
chr2:53906607 | T | C | 8 | a0001c0022 a0002c0003 a0002c0021 others(5): Show |
67 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(64): Show |
synonymous_variant | LOW | c.2934A>G | p.Ser978Ser | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 26/47 | 3143/7250 | 2934/5532 | 978/1843 | chr2 | 53906607 | |||
chr2:53919177 | C | T | 1 | a0001c0018 | 1 | HG01496.hp2 | synonymous_variant | LOW | c.2490G>A | p.Pro830Pro | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/47 | 2699/7250 | 2490/5532 | 830/1843 | chr2 | 53919177 | |||
chr2:53923100 | A | G | 4 | a0001c0005 a0001c0017 a0004c0008 others(1): Show |
56 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(53): Show |
synonymous_variant | LOW | c.1927T>C | p.Leu643Leu | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 16/47 | 2136/7250 | 1927/5532 | 643/1843 | chr2 | 53923100 | |||
chr2:53931945 | C | T | 2 | a0005c0011 a0013c0030 |
4 | HG01243.hp1 HG01891.hp2 HG02717.hp2 others(1): Show |
synonymous_variant | LOW | c.1206G>A | p.Gln402Gln | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 10/47 | 1415/7250 | 1206/5532 | 402/1843 | chr2 | 53931945 | |||
chr2:53931969 | T | C | 1 | a0002c0029 | 1 | HG03017.hp2 | synonymous_variant | LOW | c.1182A>G | p.Thr394Thr | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 10/47 | 1391/7250 | 1182/5532 | 394/1843 | chr2 | 53931969 | |||
chr2:53936108 | A | G | 1 | a0002c0015 | 1 | HG01255.hp1 | synonymous_variant | LOW | c.813T>C | p.Asp271Asp | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 7/47 | 1022/7250 | 813/5532 | 271/1843 | chr2 | 53936108 | |||
chr2:53970599 | G | A | 1 | a0002c0033 | 1 | HG03942.hp1 | synonymous_variant | LOW | c.186C>T | p.Ala62Ala | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/47 | 395/7250 | 186/5532 | 62/1843 | chr2 | 53970599 | |||
chr2:53970599 | G | C | 1 | a0002c0032 | 1 | NA18991.hp2 | synonymous_variant | LOW | c.186C>G | p.Ala62Ala | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/47 | 395/7250 | 186/5532 | 62/1843 | chr2 | 53970599 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:53864127 | A | G | 1 | a0001c0006t0014 | 1 | HG00099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1451T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 47/47 | 1962 | chr2 | 53864127 | ||||||
chr2:53864317 | C | T | 1 | a0001c0009t0013 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1261G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 47/47 | 1772 | chr2 | 53864317 | ||||||
chr2:53864433 | G | GA | 5 | a0001c0001t0007 a0001c0005t0007 a0001c0006t0015 others(2): Show |
8 | HG00621.hp1 HG02559.hp2 HG02965.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1144dupT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 47/47 | 1655 | chr2 | 53864433 | ||||||
chr2:53864433 | GA | G | 19 | a0001c0001t0012 a0001c0022t0016 a0002c0002t0002 others(16): Show |
130 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(127): Show |
3_prime_UTR_variant | MODIFIER | c.*1144delT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 47/47 | 1655 | chr2 | 53864433 | ||||||
chr2:53864551 | C | T | 21 | a0001c0022t0016 a0002c0002t0002 a0002c0002t0004 others(18): Show |
136 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*1027G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 47/47 | 1538 | chr2 | 53864551 | ||||||
chr2:53864567 | T | C | 1 | a0001c0005t0009 | 2 | NA18968.hp2 NA18971.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1011A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 47/47 | 1522 | chr2 | 53864567 | ||||||
chr2:53864611 | T | C | 8 | a0001c0001t0003 a0001c0006t0003 a0001c0006t0005 others(5): Show |
39 | HG00099.hp2 HG00738.hp2 HG01099.hp2 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*967A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 47/47 | 1478 | chr2 | 53864611 | ||||||
chr2:53864638 | ACT | A | 1 | a0001c0007t0006 | 4 | HG02559.hp2 HG02965.hp2 HG03209.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*938_*939delAG | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 47/47 | 1449 | chr2 | 53864638 | ||||||
chr2:53864748 | T | A | 21 | a0001c0022t0016 a0002c0002t0002 a0002c0002t0004 others(18): Show |
136 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*830A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 47/47 | 1341 | chr2 | 53864748 | ||||||
chr2:53865348 | CA | C | 20 | a0002c0002t0002 a0002c0002t0004 a0002c0003t0002 others(17): Show |
135 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(132): Show |
3_prime_UTR_variant | MODIFIER | c.*229delT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 47/47 | 740 | chr2 | 53865348 | ||||||
chr2:53970806 | A | C | 1 | a0002c0003t0011 | 1 | HG02602.hp1 | 5_prime_UTR_variant | MODIFIER | c.-22T>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/47 | 22 | chr2 | 53970806 | ||||||
chr2:53970857 | C | T | 1 | a0002c0003t0008 | 2 | NA18943.hp2 NA19085.hp2 |
5_prime_UTR_variant | MODIFIER | c.-73G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/47 | 73 | chr2 | 53970857 | ||||||
chr2:53970962 | C | G | 2 | a0001c0006t0005 a0002c0003t0010 |
5 | HG02109.hp1 HG02145.hp1 HG02809.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-178G>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/47 | 178 | chr2 | 53970962 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:53865614 | A | G | 1 | a0014c0026t0001g0013 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.*5-41T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 46/46 | chr2 | 53865614 | |||||||
chr2:53865847 | C | T | 243 | a0001c0001t0003g0203 a0001c0005t0001g0182 a0001c0005t0001g0311 others(240): Show |
243 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(240): Show |
intron_variant | MODIFIER | c.*4+238G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 46/46 | chr2 | 53865847 | |||||||
chr2:53866286 | T | C | 2 | a0001c0007t0001g0361 a0014c0026t0001g0013 |
2 | HG03098.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.5398-63A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 45/46 | chr2 | 53866286 | |||||||
chr2:53866361 | A | G | 2 | a0001c0006t0003g0027 a0001c0006t0003g0030 |
2 | HG01099.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.5398-138T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 45/46 | chr2 | 53866361 | |||||||
chr2:53866731 | T | C | 3 | a0001c0006t0003g0172 a0001c0006t0003g0175 a0001c0006t0003g0371 |
3 | HG02257.hp2 HG02280.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.5397+16A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 45/46 | chr2 | 53866731 | |||||||
chr2:53866908 | A | C | 1 | a0001c0005t0001g0321 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.5264-28T>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53866908 | |||||||
chr2:53866918 | A | G | 1 | a0003c0004t0001g0194 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.5264-38T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53866918 | |||||||
chr2:53866933 | T | C | 2 | a0001c0007t0001g0361 a0014c0026t0001g0013 |
2 | HG03098.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.5264-53A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53866933 | |||||||
chr2:53867106 | C | T | 1 | a0001c0009t0001g0365 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.5264-226G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53867106 | |||||||
chr2:53867147 | C | A | 37 | a0001c0006t0003g0025 a0001c0006t0003g0026 a0001c0006t0003g0027 others(34): Show |
37 | HG00099.hp2 HG00738.hp2 HG01099.hp2 others(34): Show |
intron_variant | MODIFIER | c.5264-267G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53867147 | |||||||
chr2:53867178 | G | A | 4 | a0001c0007t0006g0012 a0001c0007t0006g0014 a0001c0007t0006g0196 others(1): Show |
4 | HG02559.hp2 HG02965.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.5264-298C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53867178 | |||||||
chr2:53867230 | C | G | 3 | a0001c0006t0003g0163 a0001c0006t0003g0165 a0001c0006t0003g0166 |
3 | NA18951.hp2 NA18973.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.5264-350G>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53867230 | |||||||
chr2:53867284 | G | C | 244 | a0001c0001t0003g0203 a0001c0005t0001g0182 a0001c0005t0001g0311 others(241): Show |
244 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(241): Show |
intron_variant | MODIFIER | c.5264-404C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53867284 | |||||||
chr2:53867312 | T | C | 14 | a0001c0001t0001g0173 a0001c0001t0001g0180 a0001c0001t0001g0198 others(11): Show |
14 | HG02451.hp2 HG02486.hp2 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.5264-432A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53867312 | |||||||
chr2:53867320 | C | T | 1 | a0001c0009t0013g0292 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.5264-440G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53867320 | |||||||
chr2:53867326 | G | A | 1 | a0002c0003t0001g0079 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.5264-446C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53867326 | |||||||
chr2:53867395 | G | T | 1 | a0001c0006t0003g0160 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.5264-515C>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53867395 | |||||||
chr2:53867500 | AG | A | 61 | a0002c0002t0002g0022 a0002c0002t0002g0023 a0002c0002t0002g0043 others(58): Show |
61 | HG00280.hp2 HG00423.hp2 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.5264-621delC | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53867500 | |||||||
chr2:53867501 | G | GA | 4 | a0002c0003t0002g0146 a0002c0032t0004g0374 a0005c0011t0002g0363 others(1): Show |
4 | HG01168.hp2 HG01243.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.5264-622_5264-621i others(3): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53867501 | |||||||
chr2:53867501 | G | GAA | 42 | a0002c0003t0002g0011 a0002c0003t0002g0016 a0002c0003t0002g0020 others(39): Show |
42 | HG00408.hp2 HG00733.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.5264-622_5264-621i others(4): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53867501 | |||||||
chr2:53867501 | G | GAAA | 21 | a0001c0022t0016g0111 a0002c0003t0002g0049 a0002c0003t0002g0052 others(18): Show |
21 | HG00438.hp1 HG00558.hp1 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.5264-622_5264-621i others(5): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53867501 | |||||||
chr2:53867502 | G | A | 73 | a0001c0022t0016g0111 a0002c0002t0002g0117 a0002c0003t0002g0011 others(70): Show |
73 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.5264-622C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53867502 | |||||||
chr2:53867502 | G | GA | 73 | a0001c0001t0001g0210 a0001c0001t0001g0240 a0001c0005t0001g0311 others(70): Show |
73 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.5264-623dupT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53867502 | |||||||
chr2:53867526 | A | G | 140 | a0001c0007t0006g0012 a0001c0007t0006g0014 a0001c0007t0006g0196 others(137): Show |
140 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.5264-646T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53867526 | |||||||
chr2:53867646 | G | A | 1 | a0001c0009t0013g0292 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.5264-766C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53867646 | |||||||
chr2:53867648 | C | T | 1 | a0001c0001t0001g0277 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.5264-768G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53867648 | |||||||
chr2:53867651 | T | C | 1 | a0001c0001t0012g0041 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.5264-771A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53867651 | |||||||
chr2:53867669 | C | CA | 38 | a0001c0001t0001g0281 a0001c0001t0001g0282 a0001c0001t0001g0305 others(35): Show |
38 | HG00099.hp2 HG00738.hp2 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.5264-790dupT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53867669 | |||||||
chr2:53867669 | CA | C | 69 | a0001c0001t0001g0204 a0001c0001t0001g0238 a0001c0005t0001g0182 others(66): Show |
69 | HG00408.hp1 HG00423.hp1 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.5264-790delT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53867669 | |||||||
chr2:53867669 | CAAA | C | 67 | a0002c0002t0002g0022 a0002c0002t0002g0023 a0002c0002t0002g0043 others(64): Show |
67 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.5264-792_5264-790d others(5): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53867669 | |||||||
chr2:53867669 | CAAAA | C | 66 | a0001c0022t0016g0111 a0002c0003t0002g0011 a0002c0003t0002g0016 others(63): Show |
66 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.5264-793_5264-790d others(6): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53867669 | |||||||
chr2:53867887 | A | G | 1 | a0003c0004t0001g0254 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.5264-1007T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53867887 | |||||||
chr2:53868151 | A | G | 1 | a0001c0006t0014g0164 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.5263+1225T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53868151 | |||||||
chr2:53868180 | G | T | 65 | a0002c0003t0002g0011 a0002c0003t0002g0016 a0002c0003t0002g0019 others(62): Show |
65 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.5263+1196C>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53868180 | |||||||
chr2:53868227 | T | C | 1 | a0002c0002t0002g0141 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.5263+1149A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53868227 | |||||||
chr2:53868313 | G | A | 37 | a0001c0006t0003g0025 a0001c0006t0003g0026 a0001c0006t0003g0027 others(34): Show |
37 | HG00099.hp2 HG00738.hp2 HG01099.hp2 others(34): Show |
intron_variant | MODIFIER | c.5263+1063C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53868313 | |||||||
chr2:53868345 | G | T | 1 | a0003c0004t0001g0250 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.5263+1031C>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53868345 | |||||||
chr2:53868357 | C | A | 3 | a0001c0001t0001g0190 a0001c0001t0001g0226 a0001c0001t0001g0308 |
3 | HG01261.hp2 HG01361.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.5263+1019G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53868357 | |||||||
chr2:53868456 | AAATATAT others(100): Show |
A | 66 | a0001c0005t0001g0182 a0001c0005t0001g0311 a0001c0005t0001g0313 others(63): Show |
66 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.5263+813_5263+919d others(2): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53868456 | |||||||
chr2:53868476 | A | AT | 69 | a0002c0002t0002g0022 a0002c0002t0002g0023 a0002c0002t0002g0043 others(66): Show |
69 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.5263+899dupA | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53868476 | |||||||
chr2:53868482 | A | AAT | 15 | a0001c0001t0001g0277 a0001c0006t0003g0031 a0001c0006t0003g0155 others(12): Show |
15 | HG01167.hp2 HG01891.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.5263+892_5263+893d others(4): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53868482 | |||||||
chr2:53868482 | AAT | A | 5 | a0001c0001t0001g0035 a0001c0007t0001g0015 a0001c0007t0001g0017 others(2): Show |
5 | HG01081.hp2 HG02451.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.5263+892_5263+893d others(4): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53868482 | |||||||
chr2:53868486 | TATATATA others(62): Show |
T | 134 | a0001c0022t0016g0111 a0002c0002t0002g0022 a0002c0002t0002g0023 others(131): Show |
134 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.5263+821_5263+889d others(71): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53868486 | |||||||
chr2:53868488 | TATATATA others(60): Show |
T | 1 | a0002c0002t0002g0125 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.5263+821_5263+887d others(69): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53868488 | |||||||
chr2:53868497 | G | GATATATA others(27): Show |
1 | a0001c0006t0003g0172 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.5263+845_5263+878d others(36): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53868497 | |||||||
chr2:53868509 | A | AAAATATA others(26): Show |
32 | a0001c0001t0003g0203 a0001c0006t0003g0025 a0001c0006t0003g0026 others(29): Show |
32 | HG00099.hp2 HG00738.hp2 HG01099.hp2 others(29): Show |
intron_variant | MODIFIER | c.5263+834_5263+866d others(35): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53868509 | |||||||
chr2:53868509 | A | AAAATATA others(60): Show |
1 | a0001c0006t0003g0175 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.5263+866_5263+867i others(69): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53868509 | |||||||
chr2:53868526 | TATATAAT others(22): Show |
T | 1 | a0009c0031t0002g0021 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.5263+821_5263+849d others(31): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53868526 | |||||||
chr2:53868542 | T | TA | 15 | a0001c0006t0005g0002 a0001c0006t0005g0004 a0003c0004t0001g0040 others(12): Show |
15 | HG02132.hp1 HG02145.hp1 NA18959.hp2 others(12): Show |
intron_variant | MODIFIER | c.5263+833dupT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53868542 | |||||||
chr2:53868542 | T | TAAAATAT others(61): Show |
1 | a0001c0006t0003g0371 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.5263+833_5263+834i others(70): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53868542 | |||||||
chr2:53868564 | A | AATATATA others(26): Show |
1 | a0010c0027t0003g0162 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.5263+811_5263+812i others(35): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53868564 | |||||||
chr2:53868572 | T | A | 1 | a0001c0001t0001g0191 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.5263+804A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53868572 | |||||||
chr2:53868575 | TA | T | 7 | a0001c0001t0001g0053 a0001c0001t0001g0181 a0001c0001t0001g0239 others(4): Show |
7 | HG01243.hp1 HG01255.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.5263+800delT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53868575 | |||||||
chr2:53868576 | A | AAATATAT others(25): Show |
2 | a0001c0006t0005g0002 a0001c0006t0005g0004 |
2 | HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.5263+799_5263+800i others(34): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53868576 | |||||||
chr2:53868583 | A | AT | 5 | a0002c0002t0002g0043 a0002c0002t0002g0054 a0002c0002t0002g0081 others(2): Show |
5 | HG00280.hp2 HG00323.hp1 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.5263+792dupA | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53868583 | |||||||
chr2:53868589 | AAT | A | 3 | a0001c0001t0003g0203 a0001c0006t0003g0161 a0001c0006t0003g0178 |
3 | HG00738.hp2 HG02559.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.5263+785_5263+786d others(4): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53868589 | |||||||
chr2:53868614 | C | A | 135 | a0002c0002t0002g0022 a0002c0002t0002g0023 a0002c0002t0002g0043 others(132): Show |
135 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.5263+762G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53868614 | |||||||
chr2:53868868 | T | C | 1 | a0003c0004t0003g0218 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.5263+508A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53868868 | |||||||
chr2:53869121 | C | T | 1 | a0002c0003t0002g0059 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.5263+255G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53869121 | |||||||
chr2:53869186 | A | T | 4 | a0001c0007t0001g0015 a0001c0007t0001g0017 a0001c0007t0001g0179 others(1): Show |
4 | HG01081.hp2 HG02451.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.5263+190T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 44/46 | chr2 | 53869186 | |||||||
chr2:53869600 | AG | A | 6 | a0001c0001t0001g0053 a0001c0001t0001g0181 a0001c0001t0001g0191 others(3): Show |
6 | HG01255.hp2 HG02976.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.5101-63delC | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53869600 | |||||||
chr2:53869602 | G | C | 1 | a0003c0004t0001g0268 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.5101-64C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53869602 | |||||||
chr2:53869933 | A | G | 1 | a0001c0009t0001g0365 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.5101-395T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53869933 | |||||||
chr2:53869975 | C | T | 66 | a0002c0003t0002g0011 a0002c0003t0002g0016 a0002c0003t0002g0019 others(63): Show |
66 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.5101-437G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53869975 | |||||||
chr2:53870028 | C | T | 1 | a0016c0024t0001g0312 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.5101-490G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53870028 | |||||||
chr2:53870115 | G | A | 1 | a0001c0007t0001g0361 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.5101-577C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53870115 | |||||||
chr2:53870246 | C | T | 107 | a0001c0005t0001g0182 a0001c0005t0001g0311 a0001c0005t0001g0313 others(104): Show |
107 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.5101-708G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53870246 | |||||||
chr2:53870373 | G | GT | 29 | a0001c0001t0001g0038 a0001c0001t0001g0053 a0001c0001t0001g0181 others(26): Show |
29 | HG00609.hp2 HG01081.hp1 HG01099.hp1 others(26): Show |
intron_variant | MODIFIER | c.5101-836dupA | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53870373 | |||||||
chr2:53870373 | GT | G | 150 | a0001c0001t0001g0185 a0001c0001t0001g0273 a0001c0005t0001g0314 others(147): Show |
150 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.5101-836delA | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53870373 | |||||||
chr2:53870373 | GTT | G | 63 | a0001c0005t0001g0182 a0001c0005t0001g0311 a0001c0005t0001g0313 others(60): Show |
63 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.5101-837_5101-836d others(4): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53870373 | |||||||
chr2:53870436 | C | T | 1 | a0002c0003t0002g0144 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.5101-898G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53870436 | |||||||
chr2:53870437 | A | G | 1 | a0002c0003t0002g0144 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.5101-899T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53870437 | |||||||
chr2:53870438 | G | A | 1 | a0002c0003t0002g0144 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.5101-900C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53870438 | |||||||
chr2:53870440 | C | A | 1 | a0002c0003t0002g0144 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.5101-902G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53870440 | |||||||
chr2:53870536 | A | AT | 6 | a0001c0001t0001g0240 a0001c0001t0001g0276 a0002c0015t0002g0359 others(3): Show |
6 | HG01255.hp1 HG03486.hp2 HG04228.hp1 others(3): Show |
intron_variant | MODIFIER | c.5101-999dupA | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53870536 | |||||||
chr2:53870604 | C | T | 2 | a0001c0006t0005g0002 a0001c0006t0005g0004 |
2 | HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.5101-1066G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53870604 | |||||||
chr2:53870908 | T | A | 2 | a0001c0001t0001g0267 a0005c0011t0001g0362 |
2 | HG01891.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.5101-1370A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53870908 | |||||||
chr2:53870913 | G | A | 1 | a0002c0002t0004g0048 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.5101-1375C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53870913 | |||||||
chr2:53871094 | C | T | 3 | a0001c0007t0001g0015 a0001c0007t0001g0017 a0001c0007t0001g0179 |
3 | HG01081.hp2 HG02451.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.5101-1556G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53871094 | |||||||
chr2:53871296 | G | A | 1 | a0001c0001t0001g0035 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.5101-1758C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53871296 | |||||||
chr2:53871314 | G | A | 8 | a0004c0008t0001g0376 a0004c0008t0001g0377 a0004c0008t0001g0378 others(5): Show |
8 | HG01070.hp2 HG01109.hp2 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.5101-1776C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53871314 | |||||||
chr2:53871315 | A | C | 1 | a0002c0002t0002g0086 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.5101-1777T>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53871315 | |||||||
chr2:53871383 | T | TG | 4 | a0001c0001t0001g0035 a0001c0001t0001g0223 a0001c0001t0001g0233 others(1): Show |
4 | HG00280.hp1 HG01070.hp1 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.5101-1846dupC | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53871383 | |||||||
chr2:53871402 | C | T | 135 | a0002c0002t0002g0022 a0002c0002t0002g0023 a0002c0002t0002g0043 others(132): Show |
135 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.5101-1864G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53871402 | |||||||
chr2:53871408 | C | A | 2 | a0003c0004t0001g0201 a0003c0004t0001g0271 |
2 | NA18952.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.5101-1870G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53871408 | |||||||
chr2:53871446 | G | C | 1 | a0016c0024t0001g0312 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.5101-1908C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53871446 | |||||||
chr2:53871503 | C | T | 2 | a0005c0011t0002g0363 a0013c0030t0002g0310 |
2 | HG01243.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.5101-1965G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53871503 | |||||||
chr2:53871518 | T | C | 3 | a0002c0010t0002g0018 a0002c0010t0002g0051 a0002c0010t0002g0056 |
3 | HG02572.hp1 HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.5101-1980A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53871518 | |||||||
chr2:53871546 | G | A | 6 | a0001c0001t0001g0053 a0001c0001t0001g0181 a0001c0001t0001g0191 others(3): Show |
6 | HG01255.hp2 HG02976.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.5101-2008C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53871546 | |||||||
chr2:53871592 | T | C | 1 | a0001c0001t0001g0191 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.5101-2054A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53871592 | |||||||
chr2:53871595 | T | C | 1 | a0002c0002t0002g0151 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.5101-2057A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53871595 | |||||||
chr2:53871671 | C | A | 4 | a0001c0007t0006g0012 a0001c0007t0006g0014 a0001c0007t0006g0196 others(1): Show |
4 | HG02559.hp2 HG02965.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.5101-2133G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53871671 | |||||||
chr2:53871731 | T | C | 2 | a0002c0002t0002g0141 a0002c0002t0002g0142 |
2 | HG03669.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.5101-2193A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53871731 | |||||||
chr2:53871785 | G | A | 66 | a0001c0005t0001g0182 a0001c0005t0001g0311 a0001c0005t0001g0313 others(63): Show |
66 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.5101-2247C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53871785 | |||||||
chr2:53871984 | C | A | 140 | a0001c0007t0006g0012 a0001c0007t0006g0014 a0001c0007t0006g0196 others(137): Show |
140 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.5100+2355G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53871984 | |||||||
chr2:53872022 | A | AG | 13 | a0001c0006t0003g0167 a0002c0002t0002g0044 a0002c0002t0004g0064 others(10): Show |
13 | HG01106.hp2 HG01109.hp1 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.5100+2316dupC | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53872022 | |||||||
chr2:53872107 | G | A | 1 | a0002c0003t0002g0020 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.5100+2232C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53872107 | |||||||
chr2:53872150 | T | C | 2 | a0003c0004t0001g0033 a0003c0004t0001g0256 |
2 | HG02027.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.5100+2189A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53872150 | |||||||
chr2:53872283 | G | A | 1 | a0001c0005t0001g0321 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.5100+2056C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53872283 | |||||||
chr2:53872585 | C | CA | 66 | a0002c0002t0002g0022 a0002c0002t0002g0023 a0002c0002t0002g0043 others(63): Show |
66 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.5100+1753dupT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53872585 | |||||||
chr2:53872599 | C | T | 2 | a0001c0007t0006g0012 a0001c0007t0006g0014 |
2 | HG02559.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.5100+1740G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53872599 | |||||||
chr2:53872695 | T | C | 5 | a0003c0004t0001g0286 a0003c0004t0001g0298 a0003c0004t0001g0301 others(2): Show |
5 | NA18963.hp1 NA18964.hp2 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.5100+1644A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53872695 | |||||||
chr2:53872741 | C | CA | 62 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0038 others(59): Show |
62 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.5100+1597dupT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53872741 | |||||||
chr2:53872741 | C | CAA | 16 | a0001c0001t0001g0173 a0001c0001t0001g0198 a0001c0001t0001g0199 others(13): Show |
16 | HG01884.hp2 HG01891.hp2 HG02004.hp2 others(13): Show |
intron_variant | MODIFIER | c.5100+1596_5100+159 others(6): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53872741 | |||||||
chr2:53872741 | CA | C | 9 | a0001c0001t0001g0234 a0001c0001t0001g0241 a0001c0001t0001g0242 others(6): Show |
9 | HG02258.hp2 HG03017.hp1 HG03225.hp1 others(6): Show |
intron_variant | MODIFIER | c.5100+1597delT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53872741 | |||||||
chr2:53872741 | CAA | C | 100 | a0001c0006t0003g0025 a0001c0006t0003g0026 a0001c0006t0003g0027 others(97): Show |
100 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.5100+1596_5100+159 others(6): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53872741 | |||||||
chr2:53872741 | CAAA | C | 60 | a0001c0006t0003g0158 a0001c0006t0003g0161 a0001c0006t0003g0172 others(57): Show |
60 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.5100+1595_5100+159 others(7): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53872741 | |||||||
chr2:53872741 | CAAAA | C | 7 | a0002c0003t0002g0024 a0002c0003t0002g0049 a0002c0003t0002g0110 others(4): Show |
7 | HG00408.hp2 HG01168.hp2 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.5100+1594_5100+159 others(8): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53872741 | |||||||
chr2:53872741 | CAAAAAAA others(3): Show |
C | 66 | a0001c0005t0001g0182 a0001c0005t0001g0311 a0001c0005t0001g0313 others(63): Show |
66 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.5100+1588_5100+159 others(14): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53872741 | |||||||
chr2:53872741 | CAAAAAAA others(4): Show |
C | 1 | a0004c0008t0001g0383 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.5100+1587_5100+159 others(15): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53872741 | |||||||
chr2:53872741 | CAAAAAAA others(8): Show |
C | 4 | a0001c0007t0006g0012 a0001c0007t0006g0014 a0001c0007t0006g0196 others(1): Show |
4 | HG02559.hp2 HG02965.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.5100+1583_5100+159 others(19): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53872741 | |||||||
chr2:53872813 | G | A | 3 | a0002c0010t0002g0018 a0002c0010t0002g0051 a0002c0010t0002g0056 |
3 | HG02572.hp1 HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.5100+1526C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53872813 | |||||||
chr2:53872896 | T | TA | 9 | a0001c0001t0001g0267 a0001c0005t0001g0354 a0001c0006t0003g0025 others(6): Show |
9 | HG01099.hp2 HG01106.hp1 HG01346.hp2 others(6): Show |
intron_variant | MODIFIER | c.5100+1442dupT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53872896 | |||||||
chr2:53872896 | TA | T | 137 | a0001c0001t0001g0234 a0001c0007t0001g0361 a0002c0002t0002g0022 others(134): Show |
137 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.5100+1442delT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53872896 | |||||||
chr2:53873023 | G | T | 135 | a0002c0002t0002g0022 a0002c0002t0002g0023 a0002c0002t0002g0043 others(132): Show |
135 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.5100+1316C>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53873023 | |||||||
chr2:53873175 | A | C | 1 | a0001c0009t0013g0292 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.5100+1164T>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53873175 | |||||||
chr2:53873238 | C | CA | 68 | a0002c0003t0002g0011 a0002c0003t0002g0016 a0002c0003t0002g0019 others(65): Show |
68 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.5100+1100dupT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53873238 | |||||||
chr2:53873238 | C | CAA | 66 | a0002c0002t0002g0022 a0002c0002t0002g0023 a0002c0002t0002g0043 others(63): Show |
66 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.5100+1099_5100+110 others(6): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53873238 | |||||||
chr2:53873238 | C | CAAAAAAA others(7): Show |
4 | a0001c0007t0006g0012 a0001c0007t0006g0014 a0001c0007t0006g0196 others(1): Show |
4 | HG02559.hp2 HG02965.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.5100+1100_5100+110 others(18): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53873238 | |||||||
chr2:53873238 | C | CAAAAAAA others(8): Show |
14 | a0001c0006t0003g0031 a0001c0006t0003g0155 a0001c0006t0003g0156 others(11): Show |
14 | HG00738.hp2 HG01167.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.5100+1100_5100+110 others(19): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53873238 | |||||||
chr2:53873238 | C | CAAAAAAA others(9): Show |
70 | a0001c0005t0001g0182 a0001c0005t0001g0313 a0001c0005t0001g0314 others(67): Show |
70 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.5100+1100_5100+110 others(20): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53873238 | |||||||
chr2:53873238 | C | CAAAAAAA others(10): Show |
9 | a0001c0001t0003g0203 a0001c0005t0001g0311 a0001c0005t0001g0319 others(6): Show |
9 | HG00621.hp1 HG02145.hp1 HG02683.hp2 others(6): Show |
intron_variant | MODIFIER | c.5100+1100_5100+110 others(21): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53873238 | |||||||
chr2:53873238 | C | CAAAAAAA others(11): Show |
7 | a0001c0006t0003g0025 a0001c0006t0003g0026 a0001c0006t0003g0027 others(4): Show |
7 | HG01099.hp2 HG01106.hp1 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.5100+1100_5100+110 others(22): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53873238 | |||||||
chr2:53873238 | C | CAAAAAAA others(12): Show |
2 | a0001c0006t0003g0175 a0001c0006t0003g0371 |
2 | HG02280.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.5100+1100_5100+110 others(23): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53873238 | |||||||
chr2:53873238 | C | CAAAAAAA others(13): Show |
1 | a0001c0009t0001g0365 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.5100+1100_5100+110 others(24): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53873238 | |||||||
chr2:53873243 | A | AAAAAAAA others(10): Show |
1 | a0001c0009t0013g0292 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.5100+1095_5100+109 others(21): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53873243 | |||||||
chr2:53873247 | A | AAAAAAAA others(11): Show |
1 | a0004c0008t0001g0381 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.5100+1091_5100+109 others(22): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53873247 | |||||||
chr2:53873247 | A | AAAAAAAA others(10): Show |
1 | a0004c0008t0001g0378 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.5100+1091_5100+109 others(21): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53873247 | |||||||
chr2:53873247 | A | AAAAAAAA others(9): Show |
2 | a0004c0008t0001g0380 a0004c0008t0001g0383 |
2 | HG01256.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.5100+1091_5100+109 others(20): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53873247 | |||||||
chr2:53873248 | G | A | 5 | a0004c0008t0001g0378 a0004c0008t0001g0380 a0004c0008t0001g0381 others(2): Show |
5 | HG01070.hp2 HG01109.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.5100+1091C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53873248 | |||||||
chr2:53873249 | A | G | 1 | a0013c0030t0002g0310 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.5100+1090T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53873249 | |||||||
chr2:53873254 | A | T | 1 | a0002c0002t0004g0118 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.5100+1085T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53873254 | |||||||
chr2:53873352 | G | A | 6 | a0001c0001t0001g0053 a0001c0001t0001g0181 a0001c0001t0001g0191 others(3): Show |
6 | HG01255.hp2 HG02976.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.5100+987C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53873352 | |||||||
chr2:53873502 | C | T | 1 | a0016c0024t0001g0312 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.5100+837G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53873502 | |||||||
chr2:53873525 | G | A | 1 | a0004c0008t0001g0378 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.5100+814C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53873525 | |||||||
chr2:53873937 | CAT | C | 4 | a0001c0001t0001g0180 a0001c0001t0001g0214 a0001c0001t0001g0215 others(1): Show |
4 | HG02630.hp1 HG03130.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.5100+400_5100+401d others(4): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53873937 | |||||||
chr2:53874267 | C | T | 1 | a0001c0009t0013g0292 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.5100+72G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 43/46 | chr2 | 53874267 | |||||||
chr2:53874635 | C | T | 38 | a0001c0001t0003g0203 a0001c0006t0003g0025 a0001c0006t0003g0026 others(35): Show |
38 | HG00099.hp2 HG00738.hp2 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.4945-141G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 42/46 | chr2 | 53874635 | |||||||
chr2:53874731 | G | T | 2 | a0002c0010t0002g0018 a0002c0010t0002g0056 |
2 | HG02572.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.4945-237C>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 42/46 | chr2 | 53874731 | |||||||
chr2:53874762 | T | C | 4 | a0001c0007t0006g0012 a0001c0007t0006g0014 a0001c0007t0006g0196 others(1): Show |
4 | HG02559.hp2 HG02965.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.4945-268A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 42/46 | chr2 | 53874762 | |||||||
chr2:53874820 | C | A | 135 | a0002c0002t0002g0022 a0002c0002t0002g0023 a0002c0002t0002g0043 others(132): Show |
135 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.4945-326G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 42/46 | chr2 | 53874820 | |||||||
chr2:53874839 | G | A | 1 | a0016c0024t0001g0312 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.4945-345C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 42/46 | chr2 | 53874839 | |||||||
chr2:53874996 | C | T | 4 | a0001c0001t0001g0053 a0001c0001t0001g0181 a0001c0001t0001g0239 others(1): Show |
4 | HG01255.hp2 HG03041.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.4945-502G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 42/46 | chr2 | 53874996 | |||||||
chr2:53875233 | G | C | 1 | a0001c0001t0003g0203 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.4944+394C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 42/46 | chr2 | 53875233 | |||||||
chr2:53875273 | G | A | 1 | a0002c0033t0002g0375 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.4944+354C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 42/46 | chr2 | 53875273 | |||||||
chr2:53875854 | T | C | 69 | a0002c0002t0002g0022 a0002c0002t0002g0023 a0002c0002t0002g0043 others(66): Show |
69 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.4816-99A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53875854 | |||||||
chr2:53875947 | T | G | 2 | a0001c0006t0003g0168 a0001c0006t0003g0171 |
2 | HG02630.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.4816-192A>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53875947 | |||||||
chr2:53875953 | C | A | 1 | a0002c0002t0002g0356 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.4816-198G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53875953 | |||||||
chr2:53876065 | G | A | 1 | a0001c0009t0013g0292 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.4816-310C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53876065 | |||||||
chr2:53876128 | C | T | 2 | a0001c0001t0001g0181 a0001c0001t0001g0240 |
2 | HG01255.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.4816-373G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53876128 | |||||||
chr2:53876430 | C | T | 2 | a0001c0007t0001g0361 a0014c0026t0001g0013 |
2 | HG03098.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.4816-675G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53876430 | |||||||
chr2:53876508 | T | C | 2 | a0002c0003t0002g0060 a0002c0003t0002g0078 |
2 | HG03239.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.4816-753A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53876508 | |||||||
chr2:53876533 | AAG | A | 3 | a0002c0010t0002g0018 a0002c0010t0002g0051 a0002c0010t0002g0056 |
3 | HG02572.hp1 HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.4816-780_4816-779d others(4): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53876533 | |||||||
chr2:53876545 | C | T | 1 | a0002c0003t0010g0006 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.4816-790G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53876545 | |||||||
chr2:53876583 | T | TTA | 33 | a0001c0006t0003g0025 a0001c0006t0003g0026 a0001c0006t0003g0027 others(30): Show |
33 | HG00099.hp2 HG00738.hp2 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.4816-830_4816-829d others(4): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53876583 | |||||||
chr2:53876583 | T | TTATA | 7 | a0001c0006t0003g0155 a0001c0006t0003g0156 a0001c0006t0003g0157 others(4): Show |
7 | HG01167.hp2 HG02258.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.4816-832_4816-829d others(6): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53876583 | |||||||
chr2:53876642 | A | G | 4 | a0001c0007t0006g0012 a0001c0007t0006g0014 a0001c0007t0006g0196 others(1): Show |
4 | HG02559.hp2 HG02965.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.4816-887T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53876642 | |||||||
chr2:53876713 | A | ACTTTT | 6 | a0002c0002t0002g0044 a0002c0002t0002g0065 a0002c0002t0002g0097 others(3): Show |
6 | HG02056.hp1 NA18971.hp1 NA18972.hp2 others(3): Show |
intron_variant | MODIFIER | c.4816-959_4816-958i others(7): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53876713 | |||||||
chr2:53876713 | A | ATCCTTTT others(16): Show |
1 | a0015c0028t0001g0368 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.4816-959_4816-958i others(25): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53876713 | |||||||
chr2:53876716 | C | CT | 60 | a0001c0001t0001g0244 a0001c0001t0001g0267 a0001c0001t0003g0203 others(57): Show |
60 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.4816-962dupA | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53876716 | |||||||
chr2:53876716 | C | CTTTTTT | 7 | a0002c0002t0002g0047 a0002c0002t0002g0121 a0002c0003t0002g0059 others(4): Show |
7 | HG01168.hp2 HG02895.hp2 HG03579.hp1 others(4): Show |
intron_variant | MODIFIER | c.4816-967_4816-962d others(8): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53876716 | |||||||
chr2:53876716 | C | CTTTTTTT | 105 | a0001c0005t0009g0220 a0001c0005t0009g0221 a0002c0002t0002g0023 others(102): Show |
105 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.4816-968_4816-962d others(9): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53876716 | |||||||
chr2:53876716 | C | CTTTTTTT others(1): Show |
17 | a0001c0022t0016g0111 a0002c0002t0001g0235 a0002c0002t0002g0022 others(14): Show |
17 | HG00408.hp2 HG01069.hp1 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.4816-969_4816-962d others(10): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53876716 | |||||||
chr2:53876716 | C | CTTTTTTT others(4): Show |
1 | a0011c0016t0001g0339 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.4816-972_4816-962d others(13): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53876716 | |||||||
chr2:53876716 | C | CTTTTTTT others(5): Show |
2 | a0001c0005t0001g0349 a0001c0009t0001g0369 |
2 | HG00609.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.4816-973_4816-962d others(14): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53876716 | |||||||
chr2:53876716 | C | CTTTTTTT others(9): Show |
1 | a0001c0007t0006g0196 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.4816-977_4816-962d others(18): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53876716 | |||||||
chr2:53876716 | C | CTTTTTTT others(10): Show |
2 | a0001c0007t0006g0012 a0001c0007t0006g0014 |
2 | HG02559.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.4816-978_4816-962d others(19): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53876716 | |||||||
chr2:53876716 | C | CTTTTTTT others(11): Show |
1 | a0001c0007t0006g0197 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.4816-979_4816-962d others(20): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53876716 | |||||||
chr2:53876716 | C | CTTTTTTT others(13): Show |
5 | a0001c0005t0001g0334 a0001c0005t0001g0335 a0001c0005t0001g0336 others(2): Show |
5 | HG02293.hp1 NA18955.hp2 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.4816-981_4816-962d others(22): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53876716 | |||||||
chr2:53876716 | C | CTTTTTTT others(14): Show |
5 | a0001c0005t0001g0313 a0001c0005t0001g0314 a0001c0005t0001g0328 others(2): Show |
5 | HG01175.hp2 HG01257.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.4816-962_4816-961i others(23): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53876716 | |||||||
chr2:53876716 | C | CTTTTTTT others(15): Show |
18 | a0001c0005t0001g0311 a0001c0005t0001g0319 a0001c0005t0001g0325 others(15): Show |
18 | HG01074.hp1 HG01928.hp1 HG02004.hp1 others(15): Show |
intron_variant | MODIFIER | c.4816-962_4816-961i others(24): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53876716 | |||||||
chr2:53876716 | C | CTTTTTTT others(16): Show |
11 | a0001c0005t0001g0316 a0001c0005t0001g0317 a0001c0005t0001g0318 others(8): Show |
11 | HG00597.hp1 HG01256.hp1 HG01515.hp2 others(8): Show |
intron_variant | MODIFIER | c.4816-962_4816-961i others(25): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53876716 | |||||||
chr2:53876716 | C | CTTTTTTT others(17): Show |
5 | a0001c0005t0001g0333 a0001c0005t0001g0345 a0001c0005t0001g0348 others(2): Show |
5 | HG00423.hp1 HG01070.hp2 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.4816-962_4816-961i others(26): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53876716 | |||||||
chr2:53876716 | C | CTTTTTTT others(18): Show |
2 | a0001c0005t0001g0329 a0001c0005t0001g0373 |
2 | HG00408.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.4816-962_4816-961i others(27): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53876716 | |||||||
chr2:53876716 | C | CTTTTTTT others(19): Show |
1 | a0001c0005t0001g0182 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.4816-962_4816-961i others(28): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53876716 | |||||||
chr2:53876716 | C | CTTTTTTT others(20): Show |
1 | a0001c0005t0001g0338 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.4816-962_4816-961i others(29): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53876716 | |||||||
chr2:53876716 | C | CTTTTTTT others(22): Show |
2 | a0001c0005t0001g0315 a0001c0005t0001g0322 |
2 | HG01358.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.4816-962_4816-961i others(31): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53876716 | |||||||
chr2:53876716 | C | CTTTTTTT others(23): Show |
2 | a0001c0005t0001g0351 a0001c0005t0007g0331 |
2 | HG00621.hp1 NA18940.hp1 |
intron_variant | MODIFIER | c.4816-962_4816-961i others(32): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53876716 | |||||||
chr2:53876716 | C | CTTTTTTT others(24): Show |
1 | a0001c0005t0001g0342 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.4816-962_4816-961i others(33): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53876716 | |||||||
chr2:53876716 | C | CTTTTTTT others(27): Show |
1 | a0001c0005t0001g0324 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.4816-962_4816-961i others(36): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53876716 | |||||||
chr2:53876716 | C | CTTTTTTT others(32): Show |
1 | a0001c0005t0001g0320 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.4816-962_4816-961i others(41): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53876716 | |||||||
chr2:53876716 | C | T | 9 | a0002c0002t0002g0044 a0002c0002t0002g0065 a0002c0002t0002g0097 others(6): Show |
9 | HG02056.hp1 HG03540.hp2 NA18971.hp1 others(6): Show |
intron_variant | MODIFIER | c.4816-961G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53876716 | |||||||
chr2:53876716 | CTT | C | 36 | a0001c0006t0003g0025 a0001c0006t0003g0026 a0001c0006t0003g0027 others(33): Show |
36 | HG00099.hp2 HG00738.hp2 HG01099.hp2 others(33): Show |
intron_variant | MODIFIER | c.4816-963_4816-962d others(4): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53876716 | |||||||
chr2:53876752 | G | A | 1 | a0002c0002t0002g0357 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4816-997C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53876752 | |||||||
chr2:53876767 | G | GGAGT | 108 | a0001c0001t0001g0280 a0001c0001t0003g0203 a0001c0005t0001g0182 others(105): Show |
108 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.4816-1016_4816-101 others(8): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53876767 | |||||||
chr2:53877004 | T | C | 2 | a0001c0006t0005g0002 a0001c0006t0005g0004 |
2 | HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.4816-1249A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53877004 | |||||||
chr2:53877181 | C | T | 248 | a0001c0005t0001g0182 a0001c0005t0001g0311 a0001c0005t0001g0313 others(245): Show |
248 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.4816-1426G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53877181 | |||||||
chr2:53877247 | C | CA | 64 | a0001c0001t0001g0038 a0001c0001t0001g0173 a0001c0001t0001g0198 others(61): Show |
64 | HG00280.hp2 HG00323.hp1 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.4816-1493dupT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53877247 | |||||||
chr2:53877247 | CA | C | 16 | a0001c0001t0001g0204 a0001c0001t0001g0232 a0001c0005t0001g0323 others(13): Show |
16 | HG00438.hp1 HG00609.hp2 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.4816-1493delT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53877247 | |||||||
chr2:53877271 | T | A | 1 | a0001c0009t0001g0365 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.4816-1516A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53877271 | |||||||
chr2:53877291 | A | C | 1 | a0001c0005t0001g0326 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.4816-1536T>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53877291 | |||||||
chr2:53877291 | A | G | 1 | a0016c0024t0001g0312 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.4816-1536T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53877291 | |||||||
chr2:53877365 | A | G | 8 | a0002c0002t0002g0044 a0002c0002t0002g0065 a0002c0002t0002g0097 others(5): Show |
8 | HG02056.hp1 NA18971.hp1 NA18972.hp2 others(5): Show |
intron_variant | MODIFIER | c.4816-1610T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53877365 | |||||||
chr2:53877478 | T | C | 68 | a0001c0005t0001g0182 a0001c0005t0001g0311 a0001c0005t0001g0313 others(65): Show |
68 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.4816-1723A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53877478 | |||||||
chr2:53877509 | TA | T | 59 | a0002c0003t0001g0079 a0003c0004t0001g0032 a0003c0004t0001g0033 others(56): Show |
59 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.4816-1755delT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53877509 | |||||||
chr2:53877585 | T | G | 4 | a0001c0007t0006g0012 a0001c0007t0006g0014 a0001c0007t0006g0196 others(1): Show |
4 | HG02559.hp2 HG02965.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.4816-1830A>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53877585 | |||||||
chr2:53877591 | A | G | 65 | a0002c0002t0001g0235 a0002c0002t0002g0022 a0002c0002t0002g0023 others(62): Show |
65 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.4816-1836T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53877591 | |||||||
chr2:53877594 | T | A | 243 | a0001c0005t0001g0182 a0001c0005t0001g0311 a0001c0005t0001g0313 others(240): Show |
243 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(240): Show |
intron_variant | MODIFIER | c.4816-1839A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53877594 | |||||||
chr2:53877763 | T | G | 1 | a0001c0006t0003g0160 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.4816-2008A>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53877763 | |||||||
chr2:53878071 | A | G | 1 | a0002c0002t0002g0082 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.4816-2316T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53878071 | |||||||
chr2:53878270 | C | T | 2 | a0001c0005t0001g0315 a0001c0005t0001g0319 |
2 | HG01358.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.4816-2515G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53878270 | |||||||
chr2:53878340 | A | G | 245 | a0001c0005t0001g0182 a0001c0005t0001g0311 a0001c0005t0001g0313 others(242): Show |
245 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(242): Show |
intron_variant | MODIFIER | c.4816-2585T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53878340 | |||||||
chr2:53878341 | T | C | 5 | a0001c0006t0003g0167 a0001c0006t0003g0168 a0001c0006t0003g0170 others(2): Show |
5 | HG02630.hp2 HG02896.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.4816-2586A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53878341 | |||||||
chr2:53878353 | G | A | 38 | a0001c0006t0003g0025 a0001c0006t0003g0026 a0001c0006t0003g0027 others(35): Show |
38 | HG00099.hp2 HG00738.hp2 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.4816-2598C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53878353 | |||||||
chr2:53878366 | G | A | 1 | a0001c0001t0001g0053 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.4816-2611C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53878366 | |||||||
chr2:53878372 | T | C | 1 | a0001c0005t0001g0330 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.4816-2617A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53878372 | |||||||
chr2:53878389 | T | C | 1 | a0002c0003t0002g0106 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.4816-2634A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53878389 | |||||||
chr2:53878398 | T | C | 2 | a0001c0005t0009g0220 a0001c0005t0009g0221 |
2 | NA18968.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.4816-2643A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53878398 | |||||||
chr2:53878460 | A | T | 1 | a0003c0004t0001g0251 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.4816-2705T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53878460 | |||||||
chr2:53878461 | C | A | 1 | a0001c0009t0013g0292 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.4816-2706G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53878461 | |||||||
chr2:53878477 | C | T | 6 | a0001c0001t0001g0053 a0001c0001t0001g0181 a0001c0001t0001g0191 others(3): Show |
6 | HG01255.hp2 HG02976.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.4816-2722G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53878477 | |||||||
chr2:53878642 | G | A | 1 | a0001c0009t0013g0292 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.4816-2887C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53878642 | |||||||
chr2:53878648 | C | T | 11 | a0001c0006t0003g0025 a0001c0006t0003g0026 a0001c0006t0003g0027 others(8): Show |
11 | HG00099.hp2 HG01099.hp2 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.4816-2893G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53878648 | |||||||
chr2:53878683 | C | T | 1 | a0001c0009t0001g0365 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.4816-2928G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53878683 | |||||||
chr2:53878748 | G | C | 1 | a0014c0026t0001g0013 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.4816-2993C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53878748 | |||||||
chr2:53878819 | A | G | 3 | a0005c0011t0001g0364 a0005c0011t0002g0363 a0013c0030t0002g0310 |
3 | HG01243.hp1 HG02717.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.4816-3064T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53878819 | |||||||
chr2:53878873 | C | A | 137 | a0002c0002t0001g0235 a0002c0002t0002g0022 a0002c0002t0002g0023 others(134): Show |
137 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.4816-3118G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53878873 | |||||||
chr2:53878911 | G | A | 1 | a0002c0002t0002g0086 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.4816-3156C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53878911 | |||||||
chr2:53878912 | C | T | 1 | a0003c0004t0003g0218 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.4816-3157G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53878912 | |||||||
chr2:53878989 | G | T | 3 | a0002c0003t0002g0016 a0002c0003t0002g0059 a0002c0003t0002g0072 |
3 | NA18991.hp1 NA18995.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.4816-3234C>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53878989 | |||||||
chr2:53879037 | C | T | 1 | a0001c0005t0001g0342 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.4816-3282G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53879037 | |||||||
chr2:53879080 | T | C | 3 | a0002c0010t0002g0018 a0002c0010t0002g0051 a0002c0010t0002g0056 |
3 | HG02572.hp1 HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.4816-3325A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53879080 | |||||||
chr2:53879091 | G | A | 4 | a0001c0007t0006g0012 a0001c0007t0006g0014 a0001c0007t0006g0196 others(1): Show |
4 | HG02559.hp2 HG02965.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.4816-3336C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53879091 | |||||||
chr2:53879094 | C | T | 1 | a0002c0003t0002g0145 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.4816-3339G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53879094 | |||||||
chr2:53879139 | G | T | 1 | a0001c0006t0003g0163 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.4816-3384C>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53879139 | |||||||
chr2:53879508 | T | C | 3 | a0001c0006t0003g0172 a0001c0006t0003g0175 a0001c0006t0003g0371 |
3 | HG02257.hp2 HG02280.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.4816-3753A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53879508 | |||||||
chr2:53879589 | G | A | 11 | a0001c0006t0003g0025 a0001c0006t0003g0026 a0001c0006t0003g0027 others(8): Show |
11 | HG00099.hp2 HG01099.hp2 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.4816-3834C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53879589 | |||||||
chr2:53879671 | C | T | 2 | a0001c0006t0005g0002 a0001c0006t0005g0004 |
2 | HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.4816-3916G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53879671 | |||||||
chr2:53879679 | G | A | 1 | a0003c0004t0001g0284 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.4816-3924C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53879679 | |||||||
chr2:53879716 | C | T | 1 | a0001c0006t0003g0026 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.4816-3961G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53879716 | |||||||
chr2:53879739 | C | A | 1 | a0001c0005t0001g0337 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.4816-3984G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53879739 | |||||||
chr2:53879771 | C | T | 55 | a0001c0005t0001g0182 a0001c0005t0001g0311 a0001c0005t0001g0313 others(52): Show |
55 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.4816-4016G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53879771 | |||||||
chr2:53879801 | C | CA | 22 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0223 others(19): Show |
22 | HG00280.hp1 HG01070.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.4816-4047dupT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53879801 | |||||||
chr2:53879801 | C | CAAAAAA | 121 | a0001c0022t0016g0111 a0002c0002t0001g0235 a0002c0002t0002g0022 others(118): Show |
121 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.4816-4052_4816-404 others(10): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53879801 | |||||||
chr2:53879801 | C | CAAAAAAA | 12 | a0002c0002t0002g0045 a0002c0002t0002g0099 a0002c0002t0002g0117 others(9): Show |
12 | HG01515.hp1 HG02027.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.4816-4053_4816-404 others(11): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53879801 | |||||||
chr2:53879801 | CA | C | 70 | a0001c0001t0001g0173 a0001c0005t0001g0182 a0001c0005t0001g0314 others(67): Show |
70 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.4816-4047delT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53879801 | |||||||
chr2:53879845 | T | C | 1 | a0002c0002t0002g0357 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4816-4090A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53879845 | |||||||
chr2:53879879 | C | A | 4 | a0003c0004t0001g0262 a0003c0004t0001g0263 a0003c0004t0001g0264 others(1): Show |
4 | NA18983.hp2 NA19004.hp1 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.4816-4124G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53879879 | |||||||
chr2:53879986 | C | T | 14 | a0001c0001t0001g0173 a0001c0001t0001g0180 a0001c0001t0001g0198 others(11): Show |
14 | HG02451.hp2 HG02486.hp2 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.4816-4231G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53879986 | |||||||
chr2:53880009 | T | C | 3 | a0001c0007t0001g0015 a0001c0007t0001g0017 a0001c0007t0001g0179 |
3 | HG01081.hp2 HG02451.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.4816-4254A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53880009 | |||||||
chr2:53880120 | A | T | 1 | a0014c0026t0001g0013 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.4816-4365T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53880120 | |||||||
chr2:53880199 | A | G | 139 | a0001c0022t0016g0111 a0002c0002t0001g0235 a0002c0002t0002g0022 others(136): Show |
139 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.4816-4444T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53880199 | |||||||
chr2:53880332 | C | T | 2 | a0002c0003t0002g0138 a0002c0003t0002g0147 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.4816-4577G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53880332 | |||||||
chr2:53880508 | C | T | 1 | a0004c0008t0001g0381 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.4816-4753G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53880508 | |||||||
chr2:53880750 | G | C | 1 | a0001c0009t0001g0365 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.4815+4940C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53880750 | |||||||
chr2:53880756 | C | A | 2 | a0002c0003t0002g0060 a0002c0003t0002g0078 |
2 | HG03239.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.4815+4934G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53880756 | |||||||
chr2:53880806 | T | C | 14 | a0001c0001t0001g0173 a0001c0001t0001g0180 a0001c0001t0001g0198 others(11): Show |
14 | HG02451.hp2 HG02486.hp2 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.4815+4884A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53880806 | |||||||
chr2:53881000 | G | A | 2 | a0001c0005t0009g0220 a0001c0005t0009g0221 |
2 | NA18968.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.4815+4690C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53881000 | |||||||
chr2:53881030 | G | C | 4 | a0001c0007t0006g0012 a0001c0007t0006g0014 a0001c0007t0006g0196 others(1): Show |
4 | HG02559.hp2 HG02965.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.4815+4660C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53881030 | |||||||
chr2:53881145 | G | C | 2 | a0001c0006t0003g0174 a0001c0006t0003g0217 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.4815+4545C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53881145 | |||||||
chr2:53881185 | TATAAG | T | 3 | a0005c0011t0001g0364 a0005c0011t0002g0363 a0013c0030t0002g0310 |
3 | HG01243.hp1 HG02717.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.4815+4500_4815+450 others(9): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53881185 | |||||||
chr2:53881320 | T | G | 377 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0035 others(374): Show |
378 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(375): Show |
intron_variant | MODIFIER | c.4815+4370A>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53881320 | |||||||
chr2:53881497 | T | C | 3 | a0001c0007t0001g0015 a0001c0007t0001g0017 a0001c0007t0001g0179 |
3 | HG01081.hp2 HG02451.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.4815+4193A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53881497 | |||||||
chr2:53881586 | A | ACCTGTCA others(3): Show |
2 | a0002c0002t0002g0088 a0002c0002t0002g0121 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.4815+4094_4815+410 others(14): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53881586 | |||||||
chr2:53881602 | A | AT | 13 | a0001c0001t0001g0173 a0001c0001t0001g0198 a0001c0001t0001g0199 others(10): Show |
13 | HG02451.hp2 HG02486.hp2 HG02896.hp1 others(10): Show |
intron_variant | MODIFIER | c.4815+4087dupA | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53881602 | |||||||
chr2:53881602 | A | T | 1 | a0002c0002t0002g0043 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.4815+4088T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53881602 | |||||||
chr2:53881646 | C | T | 61 | a0001c0005t0001g0182 a0001c0005t0001g0311 a0001c0005t0001g0313 others(58): Show |
61 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.4815+4044G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53881646 | |||||||
chr2:53882102 | A | G | 106 | a0001c0005t0001g0182 a0001c0005t0001g0311 a0001c0005t0001g0313 others(103): Show |
106 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.4815+3588T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53882102 | |||||||
chr2:53882213 | G | A | 3 | a0001c0001t0001g0190 a0001c0001t0001g0226 a0001c0001t0001g0308 |
3 | HG01261.hp2 HG01361.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.4815+3477C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53882213 | |||||||
chr2:53882314 | C | A | 180 | a0001c0005t0001g0182 a0001c0005t0001g0311 a0001c0005t0001g0313 others(177): Show |
180 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.4815+3376G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53882314 | |||||||
chr2:53882319 | T | C | 10 | a0001c0001t0001g0036 a0001c0001t0001g0189 a0001c0001t0001g0190 others(7): Show |
10 | HG00733.hp1 HG01069.hp1 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.4815+3371A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53882319 | |||||||
chr2:53882357 | T | A | 14 | a0001c0001t0001g0173 a0001c0001t0001g0180 a0001c0001t0001g0198 others(11): Show |
14 | HG02451.hp2 HG02486.hp2 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.4815+3333A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53882357 | |||||||
chr2:53882493 | C | G | 6 | a0001c0009t0001g0360 a0001c0009t0001g0366 a0001c0009t0001g0367 others(3): Show |
6 | HG01074.hp1 HG02717.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.4815+3197G>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53882493 | |||||||
chr2:53882562 | G | A | 4 | a0002c0003t0002g0020 a0002c0003t0002g0077 a0002c0003t0002g0108 others(1): Show |
4 | HG01106.hp2 HG01192.hp2 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.4815+3128C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53882562 | |||||||
chr2:53882580 | A | G | 1 | a0003c0004t0001g0253 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.4815+3110T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53882580 | |||||||
chr2:53882861 | G | A | 4 | a0001c0001t0001g0180 a0001c0001t0001g0214 a0001c0001t0001g0215 others(1): Show |
4 | HG02630.hp1 HG03130.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.4815+2829C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53882861 | |||||||
chr2:53882900 | C | CA | 10 | a0001c0007t0001g0179 a0001c0007t0001g0361 a0001c0009t0001g0360 others(7): Show |
10 | HG01074.hp1 HG02451.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.4815+2789dupT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53882900 | |||||||
chr2:53882900 | C | CAA | 55 | a0001c0005t0001g0182 a0001c0005t0001g0311 a0001c0005t0001g0313 others(52): Show |
55 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.4815+2788_4815+278 others(6): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53882900 | |||||||
chr2:53882908 | AAT | A | 21 | a0002c0003t0002g0060 a0002c0003t0002g0069 a0002c0003t0002g0078 others(18): Show |
21 | HG00408.hp2 HG00438.hp1 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.4815+2780_4815+278 others(6): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53882908 | |||||||
chr2:53882909 | AT | A | 53 | a0002c0002t0002g0082 a0002c0002t0002g0356 a0002c0002t0002g0358 others(50): Show |
53 | HG00558.hp1 HG00733.hp2 HG01106.hp2 others(50): Show |
intron_variant | MODIFIER | c.4815+2780delA | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53882909 | |||||||
chr2:53882910 | T | A | 140 | a0001c0001t0003g0203 a0001c0005t0001g0182 a0001c0005t0001g0311 others(137): Show |
140 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.4815+2780A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53882910 | |||||||
chr2:53882914 | T | A | 136 | a0002c0002t0001g0235 a0002c0002t0002g0022 a0002c0002t0002g0023 others(133): Show |
136 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.4815+2776A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53882914 | |||||||
chr2:53882988 | A | G | 1 | a0001c0005t0001g0372 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.4815+2702T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53882988 | |||||||
chr2:53883333 | C | A | 2 | a0001c0007t0001g0361 a0014c0026t0001g0013 |
2 | HG03098.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.4815+2357G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53883333 | |||||||
chr2:53883442 | G | C | 59 | a0002c0003t0001g0079 a0003c0004t0001g0032 a0003c0004t0001g0033 others(56): Show |
59 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.4815+2248C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53883442 | |||||||
chr2:53883455 | G | A | 2 | a0001c0001t0001g0038 a0001c0001t0001g0278 |
2 | HG01346.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.4815+2235C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53883455 | |||||||
chr2:53883654 | A | T | 1 | a0002c0002t0002g0090 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.4815+2036T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53883654 | |||||||
chr2:53883746 | CT | C | 38 | a0001c0005t0001g0182 a0001c0006t0003g0025 a0001c0006t0003g0026 others(35): Show |
38 | HG00099.hp2 HG00738.hp2 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.4815+1943delA | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53883746 | |||||||
chr2:53883898 | T | A | 1 | a0003c0004t0001g0271 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.4815+1792A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53883898 | |||||||
chr2:53884121 | A | G | 3 | a0001c0006t0003g0161 a0001c0006t0003g0178 a0001c0006t0003g0266 |
3 | HG00738.hp2 HG01884.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.4815+1569T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53884121 | |||||||
chr2:53884171 | T | C | 1 | a0001c0005t0001g0332 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.4815+1519A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53884171 | |||||||
chr2:53884223 | T | C | 8 | a0001c0001t0001g0205 a0001c0001t0001g0228 a0001c0001t0001g0230 others(5): Show |
8 | HG00597.hp2 HG00609.hp2 NA18951.hp1 others(5): Show |
intron_variant | MODIFIER | c.4815+1467A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53884223 | |||||||
chr2:53884312 | G | A | 8 | a0004c0008t0001g0376 a0004c0008t0001g0377 a0004c0008t0001g0378 others(5): Show |
8 | HG01070.hp2 HG01109.hp2 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.4815+1378C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53884312 | |||||||
chr2:53884314 | G | A | 1 | a0016c0024t0001g0312 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.4815+1376C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53884314 | |||||||
chr2:53885475 | T | G | 2 | a0001c0001t0001g0038 a0001c0001t0001g0278 |
2 | HG01346.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.4815+215A>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53885475 | |||||||
chr2:53885599 | C | T | 1 | a0016c0024t0001g0312 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.4815+91G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 41/46 | chr2 | 53885599 | |||||||
chr2:53885827 | C | T | 1 | a0002c0002t0002g0141 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.4730-52G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 40/46 | chr2 | 53885827 | |||||||
chr2:53885916 | A | G | 2 | a0002c0003t0002g0138 a0002c0003t0002g0147 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.4730-141T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 40/46 | chr2 | 53885916 | |||||||
chr2:53885927 | A | G | 1 | a0001c0009t0013g0292 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.4730-152T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 40/46 | chr2 | 53885927 | |||||||
chr2:53885975 | T | C | 1 | a0016c0024t0001g0312 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.4730-200A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 40/46 | chr2 | 53885975 | |||||||
chr2:53886067 | T | C | 3 | a0001c0007t0001g0015 a0001c0007t0001g0017 a0001c0007t0001g0179 |
3 | HG01081.hp2 HG02451.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.4730-292A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 40/46 | chr2 | 53886067 | |||||||
chr2:53886162 | C | G | 3 | a0002c0003t0002g0016 a0002c0003t0002g0059 a0002c0003t0002g0072 |
3 | NA18991.hp1 NA18995.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.4730-387G>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 40/46 | chr2 | 53886162 | |||||||
chr2:53886233 | C | A | 1 | a0002c0003t0002g0055 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.4730-458G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 40/46 | chr2 | 53886233 | |||||||
chr2:53886304 | G | A | 1 | a0003c0004t0001g0265 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.4730-529C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 40/46 | chr2 | 53886304 | |||||||
chr2:53886335 | G | A | 1 | a0002c0003t0002g0137 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.4730-560C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 40/46 | chr2 | 53886335 | |||||||
chr2:53886531 | T | C | 1 | a0002c0003t0002g0152 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.4729+728A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 40/46 | chr2 | 53886531 | |||||||
chr2:53886676 | T | C | 1 | a0001c0001t0001g0188 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.4729+583A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 40/46 | chr2 | 53886676 | |||||||
chr2:53886703 | A | G | 1 | a0001c0009t0013g0292 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.4729+556T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 40/46 | chr2 | 53886703 | |||||||
chr2:53886765 | G | A | 1 | a0006c0012t0002g0062 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.4729+494C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 40/46 | chr2 | 53886765 | |||||||
chr2:53886782 | A | G | 1 | a0002c0003t0002g0136 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.4729+477T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 40/46 | chr2 | 53886782 | |||||||
chr2:53886828 | A | G | 1 | a0001c0001t0001g0010 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.4729+431T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 40/46 | chr2 | 53886828 | |||||||
chr2:53886829 | C | G | 1 | a0001c0001t0001g0010 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.4729+430G>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 40/46 | chr2 | 53886829 | |||||||
chr2:53886831 | G | C | 1 | a0001c0001t0001g0010 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.4729+428C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 40/46 | chr2 | 53886831 | |||||||
chr2:53886835 | A | G | 3 | a0001c0007t0001g0015 a0001c0007t0001g0017 a0001c0007t0001g0179 |
3 | HG01081.hp2 HG02451.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.4729+424T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 40/46 | chr2 | 53886835 | |||||||
chr2:53887005 | A | G | 1 | a0002c0002t0002g0124 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.4729+254T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 40/46 | chr2 | 53887005 | |||||||
chr2:53887078 | T | C | 1 | a0006c0012t0002g0062 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.4729+181A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 40/46 | chr2 | 53887078 | |||||||
chr2:53887084 | T | C | 138 | a0001c0022t0016g0111 a0002c0002t0001g0235 a0002c0002t0002g0022 others(135): Show |
138 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.4729+175A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 40/46 | chr2 | 53887084 | |||||||
chr2:53887493 | G | C | 1 | a0001c0005t0001g0334 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.4521-26C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 39/46 | chr2 | 53887493 | |||||||
chr2:53887611 | C | A | 1 | a0001c0001t0001g0241 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.4521-144G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 39/46 | chr2 | 53887611 | |||||||
chr2:53887625 | G | A | 66 | a0002c0002t0004g0123 a0002c0003t0002g0011 a0002c0003t0002g0016 others(63): Show |
66 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.4521-158C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 39/46 | chr2 | 53887625 | |||||||
chr2:53887727 | T | C | 55 | a0001c0005t0001g0182 a0001c0005t0001g0311 a0001c0005t0001g0313 others(52): Show |
55 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.4520+131A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 39/46 | chr2 | 53887727 | |||||||
chr2:53887802 | T | A | 3 | a0001c0001t0003g0203 a0001c0006t0005g0003 a0001c0006t0005g0005 |
3 | HG02109.hp1 HG02976.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.4520+56A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 39/46 | chr2 | 53887802 | |||||||
chr2:53887830 | G | A | 138 | a0002c0002t0001g0235 a0002c0002t0002g0022 a0002c0002t0002g0023 others(135): Show |
138 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.4520+28C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 39/46 | chr2 | 53887830 | |||||||
chr2:53888208 | TGAAA | T | 6 | a0001c0007t0001g0361 a0001c0007t0006g0012 a0001c0007t0006g0014 others(3): Show |
6 | HG02559.hp2 HG02965.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.4389-223_4389-220d others(6): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 38/46 | chr2 | 53888208 | |||||||
chr2:53888260 | A | G | 6 | a0001c0007t0001g0361 a0001c0007t0006g0012 a0001c0007t0006g0014 others(3): Show |
6 | HG02559.hp2 HG02965.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.4389-271T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 38/46 | chr2 | 53888260 | |||||||
chr2:53888540 | C | T | 2 | a0003c0004t0001g0192 a0003c0004t0001g0245 |
2 | HG02622.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.4388+181G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 38/46 | chr2 | 53888540 | |||||||
chr2:53888638 | G | A | 2 | a0001c0005t0001g0372 a0001c0005t0001g0373 |
2 | HG00408.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.4388+83C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 38/46 | chr2 | 53888638 | |||||||
chr2:53888676 | C | T | 38 | a0001c0001t0003g0203 a0001c0006t0003g0025 a0001c0006t0003g0026 others(35): Show |
38 | HG00099.hp2 HG00738.hp2 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.4388+45G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 38/46 | chr2 | 53888676 | |||||||
chr2:53888693 | A | G | 1 | a0002c0003t0002g0049 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.4388+28T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 38/46 | chr2 | 53888693 | |||||||
chr2:53888708 | T | A | 64 | a0001c0005t0001g0182 a0001c0005t0001g0311 a0001c0005t0001g0313 others(61): Show |
64 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.4388+13A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 38/46 | chr2 | 53888708 | |||||||
chr2:53888866 | C | T | 140 | a0001c0022t0016g0111 a0002c0002t0001g0235 a0002c0002t0002g0022 others(137): Show |
140 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.4297-54G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 37/46 | chr2 | 53888866 | |||||||
chr2:53888893 | T | A | 2 | a0002c0002t0002g0088 a0002c0002t0002g0121 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.4297-81A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 37/46 | chr2 | 53888893 | |||||||
chr2:53889095 | C | T | 1 | a0001c0001t0001g0277 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.4297-283G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 37/46 | chr2 | 53889095 | |||||||
chr2:53889150 | C | T | 38 | a0001c0001t0003g0203 a0001c0006t0003g0025 a0001c0006t0003g0026 others(35): Show |
38 | HG00099.hp2 HG00738.hp2 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.4297-338G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 37/46 | chr2 | 53889150 | |||||||
chr2:53889164 | C | A | 1 | a0002c0002t0002g0124 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.4297-352G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 37/46 | chr2 | 53889164 | |||||||
chr2:53889212 | T | C | 245 | a0001c0001t0003g0203 a0001c0005t0001g0182 a0001c0005t0001g0311 others(242): Show |
245 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(242): Show |
intron_variant | MODIFIER | c.4297-400A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 37/46 | chr2 | 53889212 | |||||||
chr2:53889326 | C | T | 16 | a0002c0003t0002g0019 a0002c0003t0002g0069 a0002c0003t0002g0105 others(13): Show |
16 | HG00438.hp1 HG00735.hp1 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.4297-514G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 37/46 | chr2 | 53889326 | |||||||
chr2:53889352 | G | C | 2 | a0001c0006t0003g0174 a0001c0006t0003g0217 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.4297-540C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 37/46 | chr2 | 53889352 | |||||||
chr2:53889387 | T | C | 1 | a0003c0004t0001g0256 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.4297-575A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 37/46 | chr2 | 53889387 | |||||||
chr2:53889544 | T | A | 1 | a0003c0004t0001g0261 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.4296+560A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 37/46 | chr2 | 53889544 | |||||||
chr2:53889663 | A | C | 140 | a0001c0022t0016g0111 a0002c0002t0001g0235 a0002c0002t0002g0022 others(137): Show |
140 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.4296+441T>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 37/46 | chr2 | 53889663 | |||||||
chr2:53889701 | T | C | 2 | a0003c0004t0001g0193 a0003c0004t0001g0250 |
2 | NA19077.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.4296+403A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 37/46 | chr2 | 53889701 | |||||||
chr2:53890006 | A | G | 1 | a0001c0001t0012g0041 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.4296+98T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 37/46 | chr2 | 53890006 | |||||||
chr2:53890023 | T | C | 1 | a0001c0009t0013g0292 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.4296+81A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 37/46 | chr2 | 53890023 | |||||||
chr2:53890058 | A | T | 1 | a0001c0001t0001g0270 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.4296+46T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 37/46 | chr2 | 53890058 | |||||||
chr2:53890624 | C | A | 1 | a0001c0001t0001g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.4192-416G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 36/46 | chr2 | 53890624 | |||||||
chr2:53890760 | G | C | 1 | a0002c0002t0002g0097 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.4192-552C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 36/46 | chr2 | 53890760 | |||||||
chr2:53890780 | A | AACTTC | 6 | a0001c0001t0001g0053 a0001c0001t0001g0181 a0001c0001t0001g0191 others(3): Show |
6 | HG01255.hp2 HG02976.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.4192-573_4192-572i others(7): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 36/46 | chr2 | 53890780 | |||||||
chr2:53890807 | C | T | 6 | a0001c0007t0001g0361 a0001c0007t0006g0012 a0001c0007t0006g0014 others(3): Show |
6 | HG02559.hp2 HG02965.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.4192-599G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 36/46 | chr2 | 53890807 | |||||||
chr2:53891014 | A | G | 258 | a0001c0001t0001g0053 a0001c0001t0001g0181 a0001c0001t0001g0191 others(255): Show |
258 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(255): Show |
intron_variant | MODIFIER | c.4192-806T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 36/46 | chr2 | 53891014 | |||||||
chr2:53891025 | T | TA | 55 | a0001c0005t0001g0182 a0001c0005t0001g0311 a0001c0005t0001g0313 others(52): Show |
55 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.4192-818dupT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 36/46 | chr2 | 53891025 | |||||||
chr2:53891092 | C | T | 3 | a0001c0001t0003g0203 a0001c0006t0005g0003 a0001c0006t0005g0005 |
3 | HG02109.hp1 HG02976.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.4192-884G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 36/46 | chr2 | 53891092 | |||||||
chr2:53891253 | G | A | 1 | a0001c0009t0001g0365 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.4192-1045C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 36/46 | chr2 | 53891253 | |||||||
chr2:53891552 | A | AT | 38 | a0001c0001t0003g0203 a0001c0006t0003g0025 a0001c0006t0003g0026 others(35): Show |
38 | HG00099.hp2 HG00738.hp2 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.4191+1255dupA | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 36/46 | chr2 | 53891552 | |||||||
chr2:53891552 | AT | A | 139 | a0002c0002t0001g0235 a0002c0002t0002g0022 a0002c0002t0002g0023 others(136): Show |
139 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.4191+1255delA | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 36/46 | chr2 | 53891552 | |||||||
chr2:53891778 | C | G | 5 | a0001c0006t0003g0167 a0001c0006t0003g0168 a0001c0006t0003g0170 others(2): Show |
5 | HG02630.hp2 HG02896.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.4191+1030G>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 36/46 | chr2 | 53891778 | |||||||
chr2:53891782 | G | A | 1 | a0001c0001t0001g0267 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.4191+1026C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 36/46 | chr2 | 53891782 | |||||||
chr2:53891858 | CA | C | 239 | a0001c0001t0001g0211 a0001c0001t0003g0203 a0001c0005t0001g0182 others(236): Show |
239 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.4191+949delT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 36/46 | chr2 | 53891858 | |||||||
chr2:53891866 | A | G | 1 | a0001c0009t0001g0365 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.4191+942T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 36/46 | chr2 | 53891866 | |||||||
chr2:53891906 | T | C | 139 | a0002c0002t0001g0235 a0002c0002t0002g0022 a0002c0002t0002g0023 others(136): Show |
139 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.4191+902A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 36/46 | chr2 | 53891906 | |||||||
chr2:53891920 | G | A | 139 | a0002c0002t0001g0235 a0002c0002t0002g0022 a0002c0002t0002g0023 others(136): Show |
139 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.4191+888C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 36/46 | chr2 | 53891920 | |||||||
chr2:53891923 | G | C | 4 | a0001c0007t0006g0012 a0001c0007t0006g0014 a0001c0007t0006g0196 others(1): Show |
4 | HG02559.hp2 HG02965.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.4191+885C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 36/46 | chr2 | 53891923 | |||||||
chr2:53891924 | G | C | 1 | a0001c0001t0001g0267 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.4191+884C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 36/46 | chr2 | 53891924 | |||||||
chr2:53892215 | C | T | 1 | a0001c0005t0001g0330 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.4191+593G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 36/46 | chr2 | 53892215 | |||||||
chr2:53892311 | G | C | 1 | a0002c0003t0002g0110 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.4191+497C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 36/46 | chr2 | 53892311 | |||||||
chr2:53892434 | C | A | 103 | a0001c0001t0003g0203 a0001c0005t0001g0182 a0001c0005t0001g0311 others(100): Show |
103 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.4191+374G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 36/46 | chr2 | 53892434 | |||||||
chr2:53892559 | C | A | 3 | a0001c0006t0005g0002 a0001c0006t0005g0004 a0003c0004t0003g0218 |
3 | HG01109.hp1 HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.4191+249G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 36/46 | chr2 | 53892559 | |||||||
chr2:53892563 | T | C | 63 | a0001c0005t0001g0182 a0001c0005t0001g0311 a0001c0005t0001g0313 others(60): Show |
63 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.4191+245A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 36/46 | chr2 | 53892563 | |||||||
chr2:53892576 | A | T | 63 | a0001c0005t0001g0182 a0001c0005t0001g0311 a0001c0005t0001g0313 others(60): Show |
63 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.4191+232T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 36/46 | chr2 | 53892576 | |||||||
chr2:53892733 | T | C | 9 | a0002c0003t0002g0024 a0002c0003t0002g0136 a0002c0003t0002g0137 others(6): Show |
9 | HG00733.hp2 HG01123.hp2 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.4191+75A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 36/46 | chr2 | 53892733 | |||||||
chr2:53893048 | G | A | 62 | a0001c0005t0001g0182 a0001c0005t0001g0311 a0001c0005t0001g0313 others(59): Show |
62 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.4039-88C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 35/46 | chr2 | 53893048 | |||||||
chr2:53893067 | A | G | 139 | a0002c0002t0001g0235 a0002c0002t0002g0022 a0002c0002t0002g0023 others(136): Show |
139 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.4039-107T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 35/46 | chr2 | 53893067 | |||||||
chr2:53893135 | T | C | 1 | a0016c0024t0001g0312 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.4039-175A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 35/46 | chr2 | 53893135 | |||||||
chr2:53893238 | AT | A | 257 | a0001c0001t0001g0053 a0001c0001t0001g0181 a0001c0001t0001g0191 others(254): Show |
257 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(254): Show |
intron_variant | MODIFIER | c.4039-279delA | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 35/46 | chr2 | 53893238 | |||||||
chr2:53893257 | C | T | 63 | a0001c0005t0001g0182 a0001c0005t0001g0311 a0001c0005t0001g0313 others(60): Show |
63 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.4039-297G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 35/46 | chr2 | 53893257 | |||||||
chr2:53893360 | G | T | 256 | a0001c0001t0001g0053 a0001c0001t0001g0181 a0001c0001t0001g0191 others(253): Show |
256 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(253): Show |
intron_variant | MODIFIER | c.4038+314C>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 35/46 | chr2 | 53893360 | |||||||
chr2:53893454 | C | T | 139 | a0002c0002t0001g0235 a0002c0002t0002g0022 a0002c0002t0002g0023 others(136): Show |
139 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.4038+220G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 35/46 | chr2 | 53893454 | |||||||
chr2:53893621 | G | A | 1 | a0003c0004t0001g0192 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.4038+53C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 35/46 | chr2 | 53893621 | |||||||
chr2:53893831 | G | A | 1 | a0002c0003t0002g0297 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3913-32C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 34/46 | chr2 | 53893831 | |||||||
chr2:53893964 | C | T | 1 | a0016c0024t0001g0312 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3913-165G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 34/46 | chr2 | 53893964 | |||||||
chr2:53894016 | G | A | 2 | a0001c0006t0005g0002 a0001c0006t0005g0004 |
2 | HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3913-217C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 34/46 | chr2 | 53894016 | |||||||
chr2:53894255 | C | A | 1 | a0001c0009t0001g0365 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3913-456G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 34/46 | chr2 | 53894255 | |||||||
chr2:53894307 | T | C | 3 | a0001c0001t0003g0203 a0001c0006t0005g0003 a0001c0006t0005g0005 |
3 | HG02109.hp1 HG02976.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.3913-508A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 34/46 | chr2 | 53894307 | |||||||
chr2:53894365 | C | T | 7 | a0001c0007t0001g0361 a0001c0007t0006g0012 a0001c0007t0006g0014 others(4): Show |
7 | HG02559.hp2 HG02965.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.3913-566G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 34/46 | chr2 | 53894365 | |||||||
chr2:53894435 | C | T | 11 | a0001c0006t0003g0031 a0001c0006t0003g0155 a0001c0006t0003g0156 others(8): Show |
11 | HG01167.hp2 HG01891.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.3912+572G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 34/46 | chr2 | 53894435 | |||||||
chr2:53894516 | C | CCTGCCTC others(98): Show |
6 | a0001c0001t0001g0053 a0001c0001t0001g0181 a0001c0001t0001g0191 others(3): Show |
6 | HG01255.hp2 HG02976.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.3912+386_3912+490d others(107): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 34/46 | chr2 | 53894516 | |||||||
chr2:53894633 | C | G | 2 | a0003c0004t0001g0202 a0003c0004t0001g0207 |
2 | NA18948.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.3912+374G>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 34/46 | chr2 | 53894633 | |||||||
chr2:53894696 | C | A | 3 | a0001c0006t0003g0172 a0001c0006t0003g0175 a0001c0006t0003g0371 |
3 | HG02257.hp2 HG02280.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.3912+311G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 34/46 | chr2 | 53894696 | |||||||
chr2:53894769 | G | A | 2 | a0001c0001t0001g0211 a0001c0001t0001g0279 |
2 | HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3912+238C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 34/46 | chr2 | 53894769 | |||||||
chr2:53894819 | T | C | 9 | a0002c0003t0002g0024 a0002c0003t0002g0136 a0002c0003t0002g0137 others(6): Show |
9 | HG00733.hp2 HG01123.hp2 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.3912+188A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 34/46 | chr2 | 53894819 | |||||||
chr2:53894823 | C | A | 37 | a0001c0006t0003g0025 a0001c0006t0003g0026 a0001c0006t0003g0027 others(34): Show |
37 | HG00099.hp2 HG00738.hp2 HG01099.hp2 others(34): Show |
intron_variant | MODIFIER | c.3912+184G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 34/46 | chr2 | 53894823 | |||||||
chr2:53895106 | C | T | 1 | a0003c0004t0001g0247 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.3843-30G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 33/46 | chr2 | 53895106 | |||||||
chr2:53895296 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.3843-220C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 33/46 | chr2 | 53895296 | |||||||
chr2:53895488 | C | T | 65 | a0002c0003t0002g0011 a0002c0003t0002g0016 a0002c0003t0002g0019 others(62): Show |
65 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.3842+95G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 33/46 | chr2 | 53895488 | |||||||
chr2:53895509 | C | T | 68 | a0002c0002t0001g0235 a0002c0002t0002g0022 a0002c0002t0002g0023 others(65): Show |
68 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.3842+74G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 33/46 | chr2 | 53895509 | |||||||
chr2:53895529 | T | C | 1 | a0002c0003t0011g0009 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.3842+54A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 33/46 | chr2 | 53895529 | |||||||
chr2:53895819 | A | G | 340 | a0001c0001t0001g0036 a0001c0001t0001g0053 a0001c0001t0001g0173 others(337): Show |
340 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(337): Show |
intron_variant | MODIFIER | c.3689-83T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 32/46 | chr2 | 53895819 | |||||||
chr2:53895832 | C | T | 1 | a0001c0009t0001g0365 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3689-96G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 32/46 | chr2 | 53895832 | |||||||
chr2:53895847 | C | T | 137 | a0002c0002t0001g0235 a0002c0002t0002g0022 a0002c0002t0002g0023 others(134): Show |
137 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.3689-111G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 32/46 | chr2 | 53895847 | |||||||
chr2:53895943 | A | T | 1 | a0001c0005t0001g0373 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.3689-207T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 32/46 | chr2 | 53895943 | |||||||
chr2:53896072 | AT | A | 7 | a0001c0007t0001g0361 a0001c0007t0006g0012 a0001c0007t0006g0014 others(4): Show |
7 | HG02559.hp2 HG02965.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.3689-337delA | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 32/46 | chr2 | 53896072 | |||||||
chr2:53896175 | C | T | 3 | a0002c0003t0002g0016 a0002c0003t0002g0059 a0002c0003t0002g0072 |
3 | NA18991.hp1 NA18995.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.3689-439G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 32/46 | chr2 | 53896175 | |||||||
chr2:53896211 | A | G | 7 | a0001c0005t0001g0333 a0001c0005t0001g0338 a0001c0005t0001g0343 others(4): Show |
7 | HG00423.hp1 HG00609.hp1 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.3689-475T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 32/46 | chr2 | 53896211 | |||||||
chr2:53896387 | C | T | 138 | a0002c0002t0001g0235 a0002c0002t0002g0022 a0002c0002t0002g0023 others(135): Show |
138 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.3688+417G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 32/46 | chr2 | 53896387 | |||||||
chr2:53896639 | T | A | 3 | a0002c0010t0002g0018 a0002c0010t0002g0051 a0002c0010t0002g0056 |
3 | HG02572.hp1 HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.3688+165A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 32/46 | chr2 | 53896639 | |||||||
chr2:53896683 | T | A | 1 | a0001c0009t0001g0365 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3688+121A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 32/46 | chr2 | 53896683 | |||||||
chr2:53896721 | T | A | 1 | a0002c0002t0002g0120 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.3688+83A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 32/46 | chr2 | 53896721 | |||||||
chr2:53897023 | T | A | 1 | a0002c0002t0002g0131 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.3607-138A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 31/46 | chr2 | 53897023 | |||||||
chr2:53897167 | G | GT | 133 | a0001c0001t0001g0035 a0001c0001t0001g0190 a0001c0001t0001g0215 others(130): Show |
133 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.3607-283dupA | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 31/46 | chr2 | 53897167 | |||||||
chr2:53897167 | G | GTT | 69 | a0001c0005t0001g0182 a0001c0005t0001g0313 a0001c0005t0001g0314 others(66): Show |
69 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.3607-284_3607-283d others(4): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 31/46 | chr2 | 53897167 | |||||||
chr2:53897167 | G | GTTT | 9 | a0001c0005t0001g0311 a0001c0005t0001g0334 a0001c0005t0001g0342 others(6): Show |
9 | HG00621.hp1 HG01074.hp1 HG01978.hp2 others(6): Show |
intron_variant | MODIFIER | c.3607-285_3607-283d others(5): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 31/46 | chr2 | 53897167 | |||||||
chr2:53897167 | G | T | 1 | a0001c0005t0001g0330 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.3607-282C>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 31/46 | chr2 | 53897167 | |||||||
chr2:53897167 | GT | G | 32 | a0001c0001t0001g0211 a0001c0001t0001g0279 a0001c0006t0003g0025 others(29): Show |
32 | HG00099.hp2 HG00738.hp2 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.3607-283delA | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 31/46 | chr2 | 53897167 | |||||||
chr2:53897167 | GTT | G | 7 | a0001c0006t0003g0168 a0001c0006t0003g0172 a0001c0006t0003g0175 others(4): Show |
7 | HG01109.hp1 HG02145.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.3607-284_3607-283d others(4): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 31/46 | chr2 | 53897167 | |||||||
chr2:53897174 | T | TG | 4 | a0005c0011t0001g0362 a0005c0011t0001g0364 a0005c0011t0002g0363 others(1): Show |
4 | HG01243.hp1 HG01891.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.3607-290_3607-289i others(3): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 31/46 | chr2 | 53897174 | |||||||
chr2:53897177 | T | G | 1 | a0001c0001t0001g0272 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.3607-292A>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 31/46 | chr2 | 53897177 | |||||||
chr2:53897258 | C | T | 1 | a0001c0006t0003g0176 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3607-373G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 31/46 | chr2 | 53897258 | |||||||
chr2:53897277 | C | T | 1 | a0002c0002t0002g0096 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.3607-392G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 31/46 | chr2 | 53897277 | |||||||
chr2:53897336 | A | G | 3 | a0002c0003t0002g0016 a0002c0003t0002g0059 a0002c0003t0002g0072 |
3 | NA18991.hp1 NA18995.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.3607-451T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 31/46 | chr2 | 53897336 | |||||||
chr2:53897555 | G | A | 1 | a0002c0003t0002g0049 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3606+315C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 31/46 | chr2 | 53897555 | |||||||
chr2:53897654 | T | C | 139 | a0001c0022t0016g0111 a0002c0002t0001g0235 a0002c0002t0002g0022 others(136): Show |
139 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.3606+216A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 31/46 | chr2 | 53897654 | |||||||
chr2:53897710 | G | C | 7 | a0001c0007t0001g0361 a0001c0007t0006g0012 a0001c0007t0006g0014 others(4): Show |
7 | HG02559.hp2 HG02965.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.3606+160C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 31/46 | chr2 | 53897710 | |||||||
chr2:53897764 | T | C | 65 | a0002c0002t0001g0235 a0002c0002t0002g0022 a0002c0002t0002g0023 others(62): Show |
65 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.3606+106A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 31/46 | chr2 | 53897764 | |||||||
chr2:53898121 | T | C | 187 | a0001c0006t0003g0025 a0001c0006t0003g0026 a0001c0006t0003g0027 others(184): Show |
187 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.3477-122A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 30/46 | chr2 | 53898121 | |||||||
chr2:53898358 | T | C | 138 | a0002c0002t0001g0235 a0002c0002t0002g0022 a0002c0002t0002g0023 others(135): Show |
138 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(135): Show |
splice_region_variant&intron_variant | LOW | c.3423-4A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 29/46 | chr2 | 53898358 | |||||||
chr2:53898387 | T | C | 1 | a0001c0009t0001g0365 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3423-33A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 29/46 | chr2 | 53898387 | |||||||
chr2:53898412 | A | G | 1 | a0001c0009t0013g0292 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3423-58T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 29/46 | chr2 | 53898412 | |||||||
chr2:53898468 | C | T | 2 | a0006c0012t0002g0057 a0006c0012t0002g0062 |
2 | HG02818.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.3423-114G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 29/46 | chr2 | 53898468 | |||||||
chr2:53898543 | C | T | 1 | a0002c0002t0001g0235 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.3423-189G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 29/46 | chr2 | 53898543 | |||||||
chr2:53898547 | T | G | 1 | a0001c0009t0001g0365 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3423-193A>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 29/46 | chr2 | 53898547 | |||||||
chr2:53898633 | G | GCA | 15 | a0001c0001t0001g0036 a0001c0001t0001g0189 a0001c0001t0001g0190 others(12): Show |
15 | HG00733.hp1 HG01069.hp1 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.3423-281_3423-280d others(4): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 29/46 | chr2 | 53898633 | |||||||
chr2:53898633 | G | GCACACAC others(5): Show |
1 | a0001c0001t0003g0203 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3423-291_3423-280d others(14): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 29/46 | chr2 | 53898633 | |||||||
chr2:53898633 | G | GTA | 57 | a0001c0005t0001g0311 a0001c0006t0003g0027 a0001c0006t0003g0161 others(54): Show |
57 | HG00423.hp2 HG00544.hp1 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.3423-280_3423-279i others(4): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 29/46 | chr2 | 53898633 | |||||||
chr2:53898633 | G | GTACA | 14 | a0001c0006t0003g0031 a0001c0006t0003g0155 a0001c0006t0003g0156 others(11): Show |
14 | HG01167.hp2 HG01891.hp1 HG02602.hp2 others(11): Show |
intron_variant | MODIFIER | c.3423-280_3423-279i others(6): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 29/46 | chr2 | 53898633 | |||||||
chr2:53898633 | GCA | G | 77 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0232 others(74): Show |
77 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.3423-281_3423-280d others(4): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 29/46 | chr2 | 53898633 | |||||||
chr2:53898633 | GCACA | G | 65 | a0001c0005t0001g0320 a0001c0005t0001g0325 a0001c0005t0001g0327 others(62): Show |
65 | HG00544.hp2 HG00558.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.3423-283_3423-280d others(6): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 29/46 | chr2 | 53898633 | |||||||
chr2:53898633 | GCACACA | G | 4 | a0001c0006t0005g0004 a0002c0002t0004g0095 a0002c0003t0002g0145 others(1): Show |
4 | HG00733.hp2 HG02015.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.3423-285_3423-280d others(8): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 29/46 | chr2 | 53898633 | |||||||
chr2:53898633 | GCACACAC others(1): Show |
G | 3 | a0001c0005t0001g0317 a0001c0005t0001g0326 a0001c0006t0005g0002 |
3 | HG00597.hp1 NA18969.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3423-287_3423-280d others(10): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 29/46 | chr2 | 53898633 | |||||||
chr2:53898633 | GCACACAC others(3): Show |
G | 2 | a0001c0009t0001g0369 a0014c0026t0001g0013 |
2 | HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.3423-289_3423-280d others(12): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 29/46 | chr2 | 53898633 | |||||||
chr2:53898634 | C | T | 82 | a0001c0005t0001g0313 a0001c0005t0001g0314 a0001c0005t0001g0315 others(79): Show |
82 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.3423-280G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 29/46 | chr2 | 53898634 | |||||||
chr2:53898636 | C | T | 64 | a0001c0005t0001g0322 a0001c0005t0001g0324 a0001c0005t0001g0332 others(61): Show |
64 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.3423-282G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 29/46 | chr2 | 53898636 | |||||||
chr2:53898638 | C | T | 12 | a0001c0005t0001g0320 a0001c0005t0001g0325 a0001c0005t0001g0327 others(9): Show |
12 | HG00609.hp1 HG00621.hp1 HG02129.hp1 others(9): Show |
intron_variant | MODIFIER | c.3423-284G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 29/46 | chr2 | 53898638 | |||||||
chr2:53898640 | C | T | 3 | a0001c0006t0005g0004 a0002c0002t0004g0095 a0002c0003t0002g0145 |
3 | HG00733.hp2 HG02145.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.3423-286G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 29/46 | chr2 | 53898640 | |||||||
chr2:53898642 | C | T | 3 | a0001c0005t0001g0317 a0001c0005t0001g0326 a0001c0006t0005g0002 |
3 | HG00597.hp1 NA18969.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3423-288G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 29/46 | chr2 | 53898642 | |||||||
chr2:53898644 | C | T | 1 | a0001c0009t0001g0369 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3423-290G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 29/46 | chr2 | 53898644 | |||||||
chr2:53898702 | T | C | 3 | a0002c0010t0002g0018 a0002c0010t0002g0051 a0002c0010t0002g0056 |
3 | HG02572.hp1 HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.3423-348A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 29/46 | chr2 | 53898702 | |||||||
chr2:53898713 | A | T | 1 | a0001c0006t0015g0169 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3423-359T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 29/46 | chr2 | 53898713 | |||||||
chr2:53898931 | C | A | 138 | a0002c0002t0001g0235 a0002c0002t0002g0022 a0002c0002t0002g0023 others(135): Show |
138 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.3423-577G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 29/46 | chr2 | 53898931 | |||||||
chr2:53899037 | G | GA | 61 | a0001c0005t0001g0182 a0001c0005t0001g0311 a0001c0005t0001g0313 others(58): Show |
61 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.3423-684dupT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 29/46 | chr2 | 53899037 | |||||||
chr2:53899127 | C | T | 2 | a0001c0006t0005g0003 a0001c0006t0005g0005 |
2 | HG02109.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.3422+754G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 29/46 | chr2 | 53899127 | |||||||
chr2:53899168 | G | A | 137 | a0002c0002t0001g0235 a0002c0002t0002g0022 a0002c0002t0002g0023 others(134): Show |
137 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.3422+713C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 29/46 | chr2 | 53899168 | |||||||
chr2:53899581 | C | G | 248 | a0001c0005t0001g0182 a0001c0005t0001g0311 a0001c0005t0001g0313 others(245): Show |
248 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.3422+300G>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 29/46 | chr2 | 53899581 | |||||||
chr2:53899622 | C | A | 238 | a0001c0005t0001g0182 a0001c0005t0001g0311 a0001c0005t0001g0313 others(235): Show |
238 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(235): Show |
intron_variant | MODIFIER | c.3422+259G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 29/46 | chr2 | 53899622 | |||||||
chr2:53900183 | AG | A | 3 | a0002c0002t0002g0087 a0002c0002t0002g0088 a0002c0002t0002g0121 |
3 | HG02622.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.3286-167delC | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 28/46 | chr2 | 53900183 | |||||||
chr2:53900330 | G | A | 1 | a0001c0017t0001g0309 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3286-313C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 28/46 | chr2 | 53900330 | |||||||
chr2:53900389 | G | GTC | 3 | a0002c0003t0002g0145 a0002c0003t0011g0009 a0002c0033t0002g0375 |
3 | HG00733.hp2 HG02602.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.3286-374_3286-373d others(4): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 28/46 | chr2 | 53900389 | |||||||
chr2:53900399 | C | CA | 7 | a0001c0005t0001g0314 a0002c0002t0002g0120 a0002c0002t0002g0122 others(4): Show |
7 | HG01069.hp2 HG01071.hp2 HG02129.hp2 others(4): Show |
intron_variant | MODIFIER | c.3286-383dupT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 28/46 | chr2 | 53900399 | |||||||
chr2:53900583 | C | T | 1 | a0001c0009t0013g0292 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3286-566G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 28/46 | chr2 | 53900583 | |||||||
chr2:53900592 | G | C | 55 | a0001c0005t0001g0182 a0001c0005t0001g0311 a0001c0005t0001g0313 others(52): Show |
55 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.3286-575C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 28/46 | chr2 | 53900592 | |||||||
chr2:53900617 | G | C | 102 | a0001c0001t0003g0203 a0001c0005t0001g0182 a0001c0005t0001g0311 others(99): Show |
102 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.3286-600C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 28/46 | chr2 | 53900617 | |||||||
chr2:53900686 | T | G | 1 | a0001c0001t0001g0236 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3285+664A>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 28/46 | chr2 | 53900686 | |||||||
chr2:53900883 | C | A | 41 | a0001c0006t0003g0025 a0001c0006t0003g0026 a0001c0006t0003g0027 others(38): Show |
41 | HG00099.hp2 HG01074.hp1 HG01099.hp2 others(38): Show |
intron_variant | MODIFIER | c.3285+467G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 28/46 | chr2 | 53900883 | |||||||
chr2:53901098 | T | C | 252 | a0001c0001t0003g0203 a0001c0005t0001g0182 a0001c0005t0001g0311 others(249): Show |
252 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(249): Show |
intron_variant | MODIFIER | c.3285+252A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 28/46 | chr2 | 53901098 | |||||||
chr2:53901177 | A | G | 1 | a0003c0004t0001g0032 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.3285+173T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 28/46 | chr2 | 53901177 | |||||||
chr2:53901182 | T | C | 66 | a0002c0002t0001g0235 a0002c0002t0002g0022 a0002c0002t0002g0023 others(63): Show |
66 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.3285+168A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 28/46 | chr2 | 53901182 | |||||||
chr2:53901572 | A | T | 3 | a0001c0006t0003g0161 a0001c0006t0003g0178 a0001c0006t0003g0266 |
3 | HG00738.hp2 HG01884.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.3076-13T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 27/46 | chr2 | 53901572 | |||||||
chr2:53902046 | G | A | 2 | a0001c0006t0003g0174 a0001c0006t0003g0217 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.3076-487C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 27/46 | chr2 | 53902046 | |||||||
chr2:53902301 | G | A | 1 | a0001c0005t0001g0182 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3076-742C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 27/46 | chr2 | 53902301 | |||||||
chr2:53902345 | T | C | 140 | a0001c0022t0016g0111 a0002c0002t0001g0235 a0002c0002t0002g0022 others(137): Show |
140 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.3076-786A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 27/46 | chr2 | 53902345 | |||||||
chr2:53902420 | A | C | 3 | a0001c0005t0001g0336 a0001c0005t0001g0341 a0001c0005t0001g0350 |
3 | NA18955.hp2 NA18986.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.3076-861T>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 27/46 | chr2 | 53902420 | |||||||
chr2:53902457 | A | G | 3 | a0005c0011t0001g0362 a0005c0011t0001g0364 a0005c0011t0002g0363 |
3 | HG01243.hp1 HG01891.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.3076-898T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 27/46 | chr2 | 53902457 | |||||||
chr2:53902477 | T | G | 3 | a0001c0007t0001g0015 a0001c0007t0001g0017 a0001c0007t0001g0179 |
3 | HG01081.hp2 HG02451.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.3076-918A>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 27/46 | chr2 | 53902477 | |||||||
chr2:53902631 | C | T | 7 | a0001c0001t0001g0205 a0001c0001t0001g0228 a0001c0001t0001g0230 others(4): Show |
7 | HG00597.hp2 HG00609.hp2 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.3076-1072G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 27/46 | chr2 | 53902631 | |||||||
chr2:53902683 | G | A | 14 | a0001c0006t0003g0031 a0001c0006t0003g0155 a0001c0006t0003g0156 others(11): Show |
14 | HG00738.hp2 HG01167.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.3076-1124C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 27/46 | chr2 | 53902683 | |||||||
chr2:53902702 | G | A | 2 | a0001c0006t0005g0002 a0001c0006t0005g0004 |
2 | HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3076-1143C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 27/46 | chr2 | 53902702 | |||||||
chr2:53903015 | G | A | 7 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0186 others(4): Show |
7 | HG00738.hp1 HG01123.hp1 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.3075+1010C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 27/46 | chr2 | 53903015 | |||||||
chr2:53903126 | C | G | 1 | a0001c0001t0001g0267 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3075+899G>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 27/46 | chr2 | 53903126 | |||||||
chr2:53903238 | A | AC | 3 | a0002c0010t0002g0018 a0002c0010t0002g0051 a0002c0010t0002g0056 |
3 | HG02572.hp1 HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.3075+786dupG | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 27/46 | chr2 | 53903238 | |||||||
chr2:53903395 | G | A | 138 | a0002c0002t0001g0235 a0002c0002t0002g0022 a0002c0002t0002g0023 others(135): Show |
138 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.3075+630C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 27/46 | chr2 | 53903395 | |||||||
chr2:53903495 | G | T | 3 | a0002c0010t0002g0018 a0002c0010t0002g0051 a0002c0010t0002g0056 |
3 | HG02572.hp1 HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.3075+530C>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 27/46 | chr2 | 53903495 | |||||||
chr2:53903670 | G | A | 7 | a0001c0007t0001g0361 a0001c0007t0006g0012 a0001c0007t0006g0014 others(4): Show |
7 | HG02559.hp2 HG02965.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.3075+355C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 27/46 | chr2 | 53903670 | |||||||
chr2:53903698 | A | C | 44 | a0001c0001t0003g0203 a0001c0006t0003g0025 a0001c0006t0003g0026 others(41): Show |
44 | HG00099.hp2 HG00738.hp2 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.3075+327T>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 27/46 | chr2 | 53903698 | |||||||
chr2:53903699 | C | T | 3 | a0001c0007t0001g0015 a0001c0007t0001g0017 a0001c0007t0001g0179 |
3 | HG01081.hp2 HG02451.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.3075+326G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 27/46 | chr2 | 53903699 | |||||||
chr2:53903748 | T | A | 1 | a0002c0003t0010g0006 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3075+277A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 27/46 | chr2 | 53903748 | |||||||
chr2:53903761 | C | G | 1 | a0001c0005t0001g0332 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.3075+264G>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 27/46 | chr2 | 53903761 | |||||||
chr2:53903867 | A | AT | 23 | a0002c0003t0001g0079 a0002c0003t0002g0019 a0002c0003t0002g0060 others(20): Show |
23 | HG00408.hp2 HG00438.hp1 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.3075+157dupA | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 27/46 | chr2 | 53903867 | |||||||
chr2:53903869 | T | TA | 44 | a0001c0001t0003g0203 a0001c0006t0003g0025 a0001c0006t0003g0026 others(41): Show |
44 | HG00099.hp2 HG00738.hp2 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.3075+155dupT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 27/46 | chr2 | 53903869 | |||||||
chr2:53903869 | TA | T | 55 | a0001c0005t0001g0182 a0001c0005t0001g0311 a0001c0005t0001g0313 others(52): Show |
55 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.3075+155delT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 27/46 | chr2 | 53903869 | |||||||
chr2:53903870 | A | T | 1 | a0003c0004t0001g0192 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3075+155T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 27/46 | chr2 | 53903870 | |||||||
chr2:53903877 | A | AT | 113 | a0002c0002t0001g0235 a0002c0002t0002g0022 a0002c0002t0002g0023 others(110): Show |
113 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.3075+147_3075+148i others(3): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 27/46 | chr2 | 53903877 | |||||||
chr2:53903877 | A | T | 23 | a0002c0003t0001g0079 a0002c0003t0002g0019 a0002c0003t0002g0060 others(20): Show |
23 | HG00408.hp2 HG00438.hp1 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.3075+148T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 27/46 | chr2 | 53903877 | |||||||
chr2:53903956 | C | T | 44 | a0001c0001t0003g0203 a0001c0006t0003g0025 a0001c0006t0003g0026 others(41): Show |
44 | HG00099.hp2 HG00738.hp2 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.3075+69G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 27/46 | chr2 | 53903956 | |||||||
chr2:53903957 | G | A | 1 | a0006c0012t0002g0057 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3075+68C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 27/46 | chr2 | 53903957 | |||||||
chr2:53904017 | C | T | 56 | a0001c0005t0001g0182 a0001c0005t0001g0311 a0001c0005t0001g0313 others(53): Show |
56 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(53): Show |
splice_region_variant&intron_variant | LOW | c.3075+8G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 27/46 | chr2 | 53904017 | |||||||
chr2:53904342 | T | C | 1 | a0001c0009t0001g0369 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2944-186A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 26/46 | chr2 | 53904342 | |||||||
chr2:53904358 | C | A | 138 | a0002c0002t0001g0235 a0002c0002t0002g0022 a0002c0002t0002g0023 others(135): Show |
138 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.2944-202G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 26/46 | chr2 | 53904358 | |||||||
chr2:53904409 | T | C | 11 | a0001c0006t0003g0025 a0001c0006t0003g0026 a0001c0006t0003g0027 others(8): Show |
11 | HG00099.hp2 HG01099.hp2 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.2944-253A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 26/46 | chr2 | 53904409 | |||||||
chr2:53904478 | G | A | 3 | a0001c0006t0005g0002 a0001c0006t0005g0004 a0003c0004t0003g0218 |
3 | HG01109.hp1 HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2944-322C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 26/46 | chr2 | 53904478 | |||||||
chr2:53904559 | T | C | 139 | a0001c0022t0016g0111 a0002c0002t0001g0235 a0002c0002t0002g0022 others(136): Show |
139 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.2944-403A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 26/46 | chr2 | 53904559 | |||||||
chr2:53904575 | C | A | 44 | a0001c0006t0003g0025 a0001c0006t0003g0026 a0001c0006t0003g0027 others(41): Show |
44 | HG00099.hp2 HG00738.hp2 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.2944-419G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 26/46 | chr2 | 53904575 | |||||||
chr2:53904620 | C | CATATTTT others(22): Show |
1 | a0002c0003t0002g0110 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2944-493_2944-465d others(31): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 26/46 | chr2 | 53904620 | |||||||
chr2:53904644 | T | A | 1 | a0001c0001t0012g0041 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2944-488A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 26/46 | chr2 | 53904644 | |||||||
chr2:53904715 | G | A | 1 | a0001c0005t0001g0343 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2944-559C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 26/46 | chr2 | 53904715 | |||||||
chr2:53904763 | T | C | 1 | a0001c0001t0001g0010 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2944-607A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 26/46 | chr2 | 53904763 | |||||||
chr2:53904770 | C | T | 1 | a0002c0002t0002g0091 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.2944-614G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 26/46 | chr2 | 53904770 | |||||||
chr2:53904858 | C | T | 1 | a0001c0005t0001g0334 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2944-702G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 26/46 | chr2 | 53904858 | |||||||
chr2:53904896 | G | A | 1 | a0003c0004t0001g0269 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2944-740C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 26/46 | chr2 | 53904896 | |||||||
chr2:53904898 | G | A | 1 | a0001c0005t0001g0337 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.2944-742C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 26/46 | chr2 | 53904898 | |||||||
chr2:53904910 | C | A | 1 | a0001c0001t0001g0173 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2944-754G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 26/46 | chr2 | 53904910 | |||||||
chr2:53905032 | T | C | 3 | a0001c0005t0001g0316 a0001c0005t0001g0318 a0001c0005t0001g0353 |
3 | HG01515.hp2 HG01517.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.2944-876A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 26/46 | chr2 | 53905032 | |||||||
chr2:53905038 | T | C | 8 | a0002c0002t0002g0050 a0002c0002t0002g0084 a0002c0002t0002g0093 others(5): Show |
8 | HG00423.hp2 HG02015.hp1 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.2944-882A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 26/46 | chr2 | 53905038 | |||||||
chr2:53905044 | G | GT | 11 | a0001c0001t0001g0035 a0001c0001t0001g0185 a0001c0001t0001g0239 others(8): Show |
11 | HG00738.hp1 HG01175.hp2 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.2944-889dupA | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 26/46 | chr2 | 53905044 | |||||||
chr2:53905136 | C | T | 139 | a0001c0022t0016g0111 a0002c0002t0001g0235 a0002c0002t0002g0022 others(136): Show |
139 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.2944-980G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 26/46 | chr2 | 53905136 | |||||||
chr2:53905197 | T | C | 1 | a0003c0004t0001g0251 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2944-1041A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 26/46 | chr2 | 53905197 | |||||||
chr2:53905257 | C | T | 1 | a0001c0019t0001g0037 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2944-1101G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 26/46 | chr2 | 53905257 | |||||||
chr2:53905403 | T | C | 139 | a0001c0022t0016g0111 a0002c0002t0001g0235 a0002c0002t0002g0022 others(136): Show |
139 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.2943+1195A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 26/46 | chr2 | 53905403 | |||||||
chr2:53905499 | G | A | 2 | a0002c0002t0002g0054 a0002c0002t0002g0085 |
2 | HG02155.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.2943+1099C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 26/46 | chr2 | 53905499 | |||||||
chr2:53905600 | G | A | 9 | a0002c0003t0002g0024 a0002c0003t0002g0136 a0002c0003t0002g0137 others(6): Show |
9 | HG00733.hp2 HG01123.hp2 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.2943+998C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 26/46 | chr2 | 53905600 | |||||||
chr2:53905721 | G | A | 2 | a0001c0006t0005g0002 a0001c0006t0005g0004 |
2 | HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2943+877C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 26/46 | chr2 | 53905721 | |||||||
chr2:53905795 | TA | T | 3 | a0001c0007t0001g0015 a0001c0007t0001g0017 a0001c0007t0001g0179 |
3 | HG01081.hp2 HG02451.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.2943+802delT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 26/46 | chr2 | 53905795 | |||||||
chr2:53906027 | T | A | 61 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0001g0295 others(58): Show |
61 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.2943+571A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 26/46 | chr2 | 53906027 | |||||||
chr2:53906080 | A | C | 1 | a0016c0024t0001g0312 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2943+518T>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 26/46 | chr2 | 53906080 | |||||||
chr2:53906203 | G | A | 1 | a0001c0005t0001g0341 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.2943+395C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 26/46 | chr2 | 53906203 | |||||||
chr2:53906501 | G | A | 44 | a0001c0006t0003g0025 a0001c0006t0003g0026 a0001c0006t0003g0027 others(41): Show |
44 | HG00099.hp2 HG00738.hp2 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.2943+97C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 26/46 | chr2 | 53906501 | |||||||
chr2:53906953 | G | T | 5 | a0001c0022t0016g0111 a0002c0003t0002g0060 a0002c0003t0002g0078 others(2): Show |
5 | HG01069.hp1 HG01515.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.2785-85C>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 24/46 | chr2 | 53906953 | |||||||
chr2:53907023 | A | G | 1 | a0001c0005t0001g0323 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2785-155T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 24/46 | chr2 | 53907023 | |||||||
chr2:53907025 | A | G | 1 | a0001c0009t0001g0365 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2785-157T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 24/46 | chr2 | 53907025 | |||||||
chr2:53907028 | A | AAT | 140 | a0001c0022t0016g0111 a0002c0002t0001g0235 a0002c0002t0002g0022 others(137): Show |
140 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.2785-162_2785-161d others(4): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 24/46 | chr2 | 53907028 | |||||||
chr2:53907036 | C | CTTAA | 140 | a0001c0022t0016g0111 a0002c0002t0001g0235 a0002c0002t0002g0022 others(137): Show |
140 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.2785-172_2785-169d others(6): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 24/46 | chr2 | 53907036 | |||||||
chr2:53907560 | C | T | 1 | a0002c0029t0002g0307 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2785-692G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 24/46 | chr2 | 53907560 | |||||||
chr2:53907801 | G | A | 1 | a0001c0001t0001g0205 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2784+519C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 24/46 | chr2 | 53907801 | |||||||
chr2:53907867 | T | A | 242 | a0001c0001t0003g0203 a0001c0005t0001g0182 a0001c0005t0001g0311 others(239): Show |
242 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(239): Show |
intron_variant | MODIFIER | c.2784+453A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 24/46 | chr2 | 53907867 | |||||||
chr2:53907915 | C | T | 242 | a0001c0001t0003g0203 a0001c0005t0001g0182 a0001c0005t0001g0311 others(239): Show |
242 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(239): Show |
intron_variant | MODIFIER | c.2784+405G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 24/46 | chr2 | 53907915 | |||||||
chr2:53908172 | C | T | 1 | a0003c0004t0001g0261 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.2784+148G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 24/46 | chr2 | 53908172 | |||||||
chr2:53908292 | G | C | 139 | a0001c0022t0016g0111 a0002c0002t0001g0235 a0002c0002t0002g0022 others(136): Show |
139 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.2784+28C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 24/46 | chr2 | 53908292 | |||||||
chr2:53908472 | G | A | 2 | a0004c0008t0001g0376 a0004c0008t0001g0379 |
2 | HG01928.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.2685+38C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 23/46 | chr2 | 53908472 | |||||||
chr2:53908628 | G | A | 1 | a0001c0005t0001g0322 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.2630-63C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 22/46 | chr2 | 53908628 | |||||||
chr2:53908967 | A | T | 8 | a0001c0006t0015g0169 a0001c0007t0001g0361 a0001c0007t0006g0012 others(5): Show |
8 | HG02559.hp2 HG02965.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.2573-127T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 21/46 | chr2 | 53908967 | |||||||
chr2:53909017 | A | G | 1 | a0003c0004t0001g0042 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2573-177T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 21/46 | chr2 | 53909017 | |||||||
chr2:53909030 | G | A | 1 | a0006c0012t0002g0057 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2573-190C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 21/46 | chr2 | 53909030 | |||||||
chr2:53909042 | T | C | 1 | a0001c0001t0001g0236 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2573-202A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 21/46 | chr2 | 53909042 | |||||||
chr2:53909124 | A | G | 1 | a0001c0005t0001g0334 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2573-284T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 21/46 | chr2 | 53909124 | |||||||
chr2:53909195 | A | G | 1 | a0001c0005t0001g0373 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2573-355T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 21/46 | chr2 | 53909195 | |||||||
chr2:53909291 | C | T | 1 | a0005c0011t0002g0363 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2573-451G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 21/46 | chr2 | 53909291 | |||||||
chr2:53909322 | T | C | 3 | a0002c0003t0002g0016 a0002c0003t0002g0059 a0002c0003t0002g0072 |
3 | NA18991.hp1 NA18995.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.2573-482A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 21/46 | chr2 | 53909322 | |||||||
chr2:53909378 | C | A | 1 | a0001c0007t0001g0361 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2573-538G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 21/46 | chr2 | 53909378 | |||||||
chr2:53909404 | T | C | 1 | a0002c0002t0002g0023 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2573-564A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 21/46 | chr2 | 53909404 | |||||||
chr2:53909419 | C | T | 1 | a0001c0001t0001g0010 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2573-579G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 21/46 | chr2 | 53909419 | |||||||
chr2:53909577 | T | C | 57 | a0001c0005t0001g0182 a0001c0005t0001g0311 a0001c0005t0001g0313 others(54): Show |
57 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.2572+498A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 21/46 | chr2 | 53909577 | |||||||
chr2:53909708 | C | T | 1 | a0001c0007t0001g0179 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2572+367G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 21/46 | chr2 | 53909708 | |||||||
chr2:53909714 | C | T | 13 | a0003c0004t0001g0040 a0003c0004t0001g0257 a0003c0004t0001g0274 others(10): Show |
13 | HG02132.hp1 NA18959.hp2 NA18963.hp1 others(10): Show |
intron_variant | MODIFIER | c.2572+361G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 21/46 | chr2 | 53909714 | |||||||
chr2:53909726 | C | T | 1 | a0003c0004t0001g0183 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2572+349G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 21/46 | chr2 | 53909726 | |||||||
chr2:53909999 | A | G | 66 | a0002c0002t0001g0235 a0002c0002t0002g0022 a0002c0002t0002g0023 others(63): Show |
66 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.2572+76T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 21/46 | chr2 | 53909999 | |||||||
chr2:53910270 | G | C | 1 | a0001c0009t0001g0365 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2517-140C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53910270 | |||||||
chr2:53910398 | A | T | 1 | a0001c0001t0001g0267 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2517-268T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53910398 | |||||||
chr2:53910689 | C | A | 3 | a0001c0006t0003g0172 a0001c0006t0003g0175 a0001c0006t0003g0371 |
3 | HG02257.hp2 HG02280.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.2517-559G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53910689 | |||||||
chr2:53910879 | G | C | 1 | a0002c0003t0002g0109 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2517-749C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53910879 | |||||||
chr2:53911113 | T | C | 7 | a0001c0007t0001g0361 a0001c0007t0006g0012 a0001c0007t0006g0014 others(4): Show |
7 | HG02559.hp2 HG02965.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.2517-983A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53911113 | |||||||
chr2:53911305 | G | T | 240 | a0001c0001t0001g0173 a0001c0001t0003g0203 a0001c0005t0001g0182 others(237): Show |
240 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.2517-1175C>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53911305 | |||||||
chr2:53911499 | C | T | 1 | a0003c0004t0001g0033 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2517-1369G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53911499 | |||||||
chr2:53911500 | G | A | 1 | a0001c0001t0001g0236 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2517-1370C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53911500 | |||||||
chr2:53911596 | G | A | 1 | a0005c0011t0002g0363 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2517-1466C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53911596 | |||||||
chr2:53911739 | A | G | 1 | a0001c0001t0001g0277 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2517-1609T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53911739 | |||||||
chr2:53911801 | A | T | 8 | a0001c0001t0001g0173 a0001c0006t0003g0155 a0001c0006t0003g0156 others(5): Show |
8 | HG01167.hp2 HG02258.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.2517-1671T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53911801 | |||||||
chr2:53911857 | G | C | 1 | a0016c0024t0001g0312 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2517-1727C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53911857 | |||||||
chr2:53911880 | T | C | 139 | a0001c0022t0016g0111 a0002c0002t0001g0235 a0002c0002t0002g0022 others(136): Show |
139 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.2517-1750A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53911880 | |||||||
chr2:53911962 | G | A | 1 | a0011c0016t0001g0339 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2517-1832C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53911962 | |||||||
chr2:53912014 | G | C | 1 | a0001c0001t0001g0267 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2517-1884C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53912014 | |||||||
chr2:53912221 | T | C | 3 | a0001c0007t0001g0015 a0001c0007t0001g0017 a0001c0007t0001g0179 |
3 | HG01081.hp2 HG02451.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.2517-2091A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53912221 | |||||||
chr2:53912313 | G | A | 2 | a0002c0003t0002g0112 a0002c0003t0002g0133 |
2 | HG01175.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.2517-2183C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53912313 | |||||||
chr2:53912422 | T | C | 65 | a0002c0002t0001g0235 a0002c0002t0002g0022 a0002c0002t0002g0023 others(62): Show |
65 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.2517-2292A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53912422 | |||||||
chr2:53912525 | A | G | 2 | a0001c0009t0001g0369 a0015c0028t0001g0368 |
2 | HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2517-2395T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53912525 | |||||||
chr2:53912676 | A | G | 2 | a0006c0012t0002g0057 a0006c0012t0002g0062 |
2 | HG02818.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.2517-2546T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53912676 | |||||||
chr2:53912758 | A | G | 261 | a0001c0001t0001g0053 a0001c0001t0001g0173 a0001c0001t0001g0181 others(258): Show |
261 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(258): Show |
intron_variant | MODIFIER | c.2517-2628T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53912758 | |||||||
chr2:53913053 | T | C | 7 | a0001c0007t0001g0361 a0001c0007t0006g0012 a0001c0007t0006g0014 others(4): Show |
7 | HG02559.hp2 HG02965.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.2517-2923A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53913053 | |||||||
chr2:53913331 | C | T | 1 | a0001c0006t0015g0169 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2517-3201G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53913331 | |||||||
chr2:53913347 | A | T | 5 | a0001c0009t0001g0360 a0001c0009t0001g0366 a0001c0009t0001g0367 others(2): Show |
5 | HG02717.hp1 HG02818.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2517-3217T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53913347 | |||||||
chr2:53913438 | C | G | 55 | a0001c0005t0001g0182 a0001c0005t0001g0311 a0001c0005t0001g0313 others(52): Show |
55 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.2517-3308G>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53913438 | |||||||
chr2:53913474 | T | C | 1 | a0002c0003t0002g0109 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2517-3344A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53913474 | |||||||
chr2:53913711 | C | A | 8 | a0002c0002t0002g0050 a0002c0002t0002g0084 a0002c0002t0002g0093 others(5): Show |
8 | HG00423.hp2 HG02015.hp1 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.2517-3581G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53913711 | |||||||
chr2:53914248 | T | C | 1 | a0001c0009t0001g0360 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2517-4118A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53914248 | |||||||
chr2:53914355 | G | A | 68 | a0002c0002t0001g0235 a0002c0002t0002g0022 a0002c0002t0002g0023 others(65): Show |
68 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.2517-4225C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53914355 | |||||||
chr2:53914441 | T | C | 1 | a0002c0010t0002g0051 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2517-4311A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53914441 | |||||||
chr2:53914500 | G | C | 46 | a0001c0001t0001g0173 a0001c0001t0003g0203 a0001c0006t0003g0025 others(43): Show |
46 | HG00099.hp2 HG00738.hp2 HG01074.hp1 others(43): Show |
intron_variant | MODIFIER | c.2517-4370C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53914500 | |||||||
chr2:53914609 | G | A | 3 | a0001c0001t0001g0190 a0001c0001t0001g0226 a0001c0001t0001g0308 |
3 | HG01261.hp2 HG01361.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.2517-4479C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53914609 | |||||||
chr2:53914621 | G | A | 1 | a0001c0017t0001g0309 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2517-4491C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53914621 | |||||||
chr2:53914693 | C | A | 55 | a0001c0005t0001g0182 a0001c0005t0001g0311 a0001c0005t0001g0313 others(52): Show |
55 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.2516+4458G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53914693 | |||||||
chr2:53914774 | G | A | 3 | a0001c0005t0001g0316 a0001c0005t0001g0318 a0001c0005t0001g0353 |
3 | HG01515.hp2 HG01517.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.2516+4377C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53914774 | |||||||
chr2:53914791 | G | C | 2 | a0001c0005t0001g0336 a0001c0005t0001g0350 |
2 | NA18955.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.2516+4360C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53914791 | |||||||
chr2:53914824 | T | A | 2 | a0001c0007t0001g0017 a0001c0007t0001g0179 |
2 | HG02451.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.2516+4327A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53914824 | |||||||
chr2:53914893 | T | C | 46 | a0001c0001t0001g0173 a0001c0001t0003g0203 a0001c0006t0003g0025 others(43): Show |
46 | HG00099.hp2 HG00738.hp2 HG01074.hp1 others(43): Show |
intron_variant | MODIFIER | c.2516+4258A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53914893 | |||||||
chr2:53915216 | A | C | 1 | a0002c0003t0002g0152 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.2516+3935T>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53915216 | |||||||
chr2:53915267 | C | T | 56 | a0001c0005t0001g0182 a0001c0005t0001g0311 a0001c0005t0001g0313 others(53): Show |
56 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.2516+3884G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53915267 | |||||||
chr2:53915276 | A | C | 1 | a0001c0006t0003g0217 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2516+3875T>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53915276 | |||||||
chr2:53915313 | C | T | 2 | a0001c0007t0001g0361 a0016c0024t0001g0312 |
2 | HG03139.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2516+3838G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53915313 | |||||||
chr2:53915542 | T | C | 139 | a0001c0022t0016g0111 a0002c0002t0001g0235 a0002c0002t0002g0022 others(136): Show |
139 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.2516+3609A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53915542 | |||||||
chr2:53915553 | T | G | 1 | a0002c0003t0002g0066 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2516+3598A>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53915553 | |||||||
chr2:53915572 | T | C | 2 | a0002c0002t0002g0356 a0002c0002t0002g0358 |
2 | HG02615.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2516+3579A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53915572 | |||||||
chr2:53915687 | G | A | 1 | a0001c0009t0001g0365 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2516+3464C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53915687 | |||||||
chr2:53915760 | T | G | 1 | a0001c0001t0012g0041 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2516+3391A>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53915760 | |||||||
chr2:53915803 | G | A | 1 | a0003c0004t0001g0253 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2516+3348C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53915803 | |||||||
chr2:53915806 | C | G | 1 | a0002c0015t0002g0359 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2516+3345G>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53915806 | |||||||
chr2:53915890 | G | T | 2 | a0001c0001t0001g0204 a0001c0001t0001g0238 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2516+3261C>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53915890 | |||||||
chr2:53915958 | C | G | 1 | a0003c0004t0001g0201 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.2516+3193G>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53915958 | |||||||
chr2:53915992 | T | G | 3 | a0001c0006t0003g0031 a0001c0006t0003g0176 a0001c0006t0003g0177 |
3 | HG02615.hp1 HG02970.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2516+3159A>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53915992 | |||||||
chr2:53916008 | G | C | 5 | a0001c0007t0006g0012 a0001c0007t0006g0014 a0001c0007t0006g0196 others(2): Show |
5 | HG02559.hp2 HG02965.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.2516+3143C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53916008 | |||||||
chr2:53916027 | A | G | 2 | a0002c0002t0002g0355 a0002c0029t0002g0307 |
2 | HG02015.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.2516+3124T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53916027 | |||||||
chr2:53916084 | T | A | 4 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0001g0295 others(1): Show |
4 | HG00099.hp1 HG01081.hp1 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.2516+3067A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53916084 | |||||||
chr2:53916185 | C | T | 46 | a0001c0001t0001g0173 a0001c0001t0003g0203 a0001c0006t0003g0025 others(43): Show |
46 | HG00099.hp2 HG00738.hp2 HG01074.hp1 others(43): Show |
intron_variant | MODIFIER | c.2516+2966G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53916185 | |||||||
chr2:53916198 | G | A | 1 | a0001c0009t0001g0365 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2516+2953C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53916198 | |||||||
chr2:53916241 | C | CA | 11 | a0001c0001t0001g0223 a0001c0001t0001g0227 a0001c0001t0001g0242 others(8): Show |
11 | HG00408.hp1 HG01070.hp1 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.2516+2909dupT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53916241 | |||||||
chr2:53916241 | C | CAAA | 74 | a0001c0001t0001g0038 a0001c0001t0001g0173 a0001c0001t0001g0184 others(71): Show |
74 | HG00099.hp2 HG00609.hp1 HG00738.hp2 others(71): Show |
intron_variant | MODIFIER | c.2516+2907_2516+290 others(7): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53916241 | |||||||
chr2:53916271 | T | C | 4 | a0001c0005t0001g0320 a0001c0005t0001g0324 a0001c0005t0001g0332 others(1): Show |
4 | HG00621.hp1 HG02132.hp2 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.2516+2880A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53916271 | |||||||
chr2:53916294 | G | C | 1 | a0002c0003t0002g0019 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2516+2857C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53916294 | |||||||
chr2:53916378 | A | G | 1 | a0003c0004t0001g0207 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.2516+2773T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53916378 | |||||||
chr2:53916431 | C | T | 63 | a0002c0002t0002g0022 a0002c0002t0002g0023 a0002c0002t0002g0043 others(60): Show |
63 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.2516+2720G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53916431 | |||||||
chr2:53916493 | T | C | 24 | a0001c0022t0016g0111 a0002c0003t0001g0079 a0002c0003t0002g0019 others(21): Show |
24 | HG00408.hp2 HG00438.hp1 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.2516+2658A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53916493 | |||||||
chr2:53916649 | A | G | 51 | a0003c0004t0001g0032 a0003c0004t0001g0033 a0003c0004t0001g0034 others(48): Show |
51 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.2516+2502T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53916649 | |||||||
chr2:53916745 | A | T | 1 | a0001c0006t0015g0169 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2516+2406T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53916745 | |||||||
chr2:53916913 | C | G | 3 | a0002c0010t0002g0018 a0002c0010t0002g0051 a0002c0010t0002g0056 |
3 | HG02572.hp1 HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2516+2238G>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53916913 | |||||||
chr2:53917057 | TTAAG | T | 138 | a0001c0022t0016g0111 a0002c0002t0002g0022 a0002c0002t0002g0023 others(135): Show |
138 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.2516+2090_2516+209 others(8): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53917057 | |||||||
chr2:53917131 | T | G | 2 | a0001c0005t0001g0315 a0001c0005t0001g0319 |
2 | HG01358.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.2516+2020A>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53917131 | |||||||
chr2:53917277 | C | T | 4 | a0003c0004t0001g0262 a0003c0004t0001g0263 a0003c0004t0001g0264 others(1): Show |
4 | NA18983.hp2 NA19004.hp1 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.2516+1874G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53917277 | |||||||
chr2:53917307 | T | C | 1 | a0002c0015t0002g0359 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2516+1844A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53917307 | |||||||
chr2:53917311 | T | C | 71 | a0001c0022t0016g0111 a0002c0003t0001g0079 a0002c0003t0002g0011 others(68): Show |
71 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.2516+1840A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53917311 | |||||||
chr2:53917375 | T | C | 7 | a0001c0005t0001g0333 a0001c0005t0001g0338 a0001c0005t0001g0343 others(4): Show |
7 | HG00423.hp1 HG00609.hp1 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.2516+1776A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53917375 | |||||||
chr2:53917395 | A | G | 67 | a0001c0022t0016g0111 a0002c0003t0001g0079 a0002c0003t0002g0011 others(64): Show |
67 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.2516+1756T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53917395 | |||||||
chr2:53917609 | C | T | 1 | a0001c0007t0001g0361 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2516+1542G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53917609 | |||||||
chr2:53917682 | T | C | 46 | a0001c0001t0001g0173 a0001c0001t0003g0203 a0001c0006t0003g0025 others(43): Show |
46 | HG00099.hp2 HG00738.hp2 HG01074.hp1 others(43): Show |
intron_variant | MODIFIER | c.2516+1469A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53917682 | |||||||
chr2:53917695 | A | C | 3 | a0001c0007t0001g0015 a0001c0007t0001g0017 a0001c0007t0001g0179 |
3 | HG01081.hp2 HG02451.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.2516+1456T>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53917695 | |||||||
chr2:53917944 | A | C | 4 | a0001c0001t0001g0180 a0001c0001t0001g0214 a0001c0001t0001g0215 others(1): Show |
4 | HG02630.hp1 HG03130.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.2516+1207T>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53917944 | |||||||
chr2:53917945 | T | C | 3 | a0001c0007t0001g0015 a0001c0007t0001g0017 a0001c0007t0001g0179 |
3 | HG01081.hp2 HG02451.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.2516+1206A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53917945 | |||||||
chr2:53918030 | T | G | 2 | a0002c0003t0002g0058 a0002c0003t0002g0074 |
2 | HG03579.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2516+1121A>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53918030 | |||||||
chr2:53918182 | G | T | 1 | a0001c0001t0001g0010 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2516+969C>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53918182 | |||||||
chr2:53918226 | G | A | 56 | a0001c0005t0001g0182 a0001c0005t0001g0311 a0001c0005t0001g0313 others(53): Show |
56 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.2516+925C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53918226 | |||||||
chr2:53918499 | G | A | 67 | a0001c0022t0016g0111 a0002c0003t0001g0079 a0002c0003t0002g0011 others(64): Show |
67 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.2516+652C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53918499 | |||||||
chr2:53918624 | T | C | 139 | a0001c0022t0016g0111 a0002c0002t0002g0022 a0002c0002t0002g0023 others(136): Show |
139 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.2516+527A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53918624 | |||||||
chr2:53918682 | G | A | 2 | a0002c0002t0002g0356 a0002c0002t0002g0358 |
2 | HG02615.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2516+469C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53918682 | |||||||
chr2:53918780 | A | T | 7 | a0001c0007t0001g0361 a0001c0007t0006g0012 a0001c0007t0006g0014 others(4): Show |
7 | HG02559.hp2 HG02965.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.2516+371T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53918780 | |||||||
chr2:53918819 | C | T | 2 | a0001c0005t0001g0326 a0001c0005t0001g0345 |
2 | HG00597.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.2516+332G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53918819 | |||||||
chr2:53918823 | C | T | 2 | a0001c0001t0001g0242 a0001c0001t0001g0282 |
2 | HG03704.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.2516+328G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53918823 | |||||||
chr2:53919037 | T | G | 2 | a0001c0006t0005g0002 a0001c0006t0005g0004 |
2 | HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2516+114A>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53919037 | |||||||
chr2:53919041 | A | G | 1 | a0005c0011t0002g0363 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2516+110T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 20/46 | chr2 | 53919041 | |||||||
chr2:53919330 | G | A | 1 | a0002c0003t0002g0055 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2421-84C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 19/46 | chr2 | 53919330 | |||||||
chr2:53919390 | A | G | 5 | a0002c0003t0002g0049 a0002c0003t0002g0055 a0002c0003t0002g0058 others(2): Show |
5 | HG02809.hp1 HG02970.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.2421-144T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 19/46 | chr2 | 53919390 | |||||||
chr2:53919489 | T | G | 1 | a0002c0002t0002g0087 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2421-243A>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 19/46 | chr2 | 53919489 | |||||||
chr2:53919583 | T | C | 3 | a0001c0006t0005g0002 a0001c0006t0005g0004 a0003c0004t0003g0218 |
3 | HG01109.hp1 HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2421-337A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 19/46 | chr2 | 53919583 | |||||||
chr2:53919628 | G | A | 1 | a0001c0006t0003g0217 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2421-382C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 19/46 | chr2 | 53919628 | |||||||
chr2:53919638 | C | T | 8 | a0004c0008t0001g0376 a0004c0008t0001g0377 a0004c0008t0001g0378 others(5): Show |
8 | HG01070.hp2 HG01109.hp2 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.2421-392G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 19/46 | chr2 | 53919638 | |||||||
chr2:53919658 | A | G | 2 | a0001c0005t0001g0317 a0001c0005t0001g0329 |
2 | HG02129.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.2421-412T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 19/46 | chr2 | 53919658 | |||||||
chr2:53919816 | G | GA | 57 | a0001c0005t0001g0182 a0001c0005t0001g0311 a0001c0005t0001g0313 others(54): Show |
57 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.2420+376dupT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 19/46 | chr2 | 53919816 | |||||||
chr2:53919925 | A | G | 1 | a0001c0009t0013g0292 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2420+268T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 19/46 | chr2 | 53919925 | |||||||
chr2:53920043 | CA | C | 3 | a0002c0002t0002g0043 a0002c0002t0002g0081 a0002c0002t0002g0083 |
3 | HG00280.hp2 HG00323.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.2420+149delT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 19/46 | chr2 | 53920043 | |||||||
chr2:53920101 | G | A | 1 | a0002c0002t0001g0235 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2420+92C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 19/46 | chr2 | 53920101 | |||||||
chr2:53920680 | G | C | 138 | a0002c0002t0002g0022 a0002c0002t0002g0023 a0002c0002t0002g0043 others(135): Show |
138 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.2262+209C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 18/46 | chr2 | 53920680 | |||||||
chr2:53920769 | A | G | 2 | a0002c0003t0002g0058 a0002c0003t0002g0074 |
2 | HG03579.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2262+120T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 18/46 | chr2 | 53920769 | |||||||
chr2:53920784 | T | A | 4 | a0005c0011t0001g0362 a0005c0011t0001g0364 a0005c0011t0002g0363 others(1): Show |
4 | HG01243.hp1 HG01891.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.2262+105A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 18/46 | chr2 | 53920784 | |||||||
chr2:53921173 | G | C | 4 | a0002c0003t0002g0020 a0002c0003t0002g0077 a0002c0003t0002g0108 others(1): Show |
4 | HG01106.hp2 HG01192.hp2 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.2047-69C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 17/46 | chr2 | 53921173 | |||||||
chr2:53921194 | C | A | 241 | a0001c0001t0001g0173 a0001c0001t0003g0203 a0001c0005t0001g0182 others(238): Show |
241 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(238): Show |
intron_variant | MODIFIER | c.2047-90G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 17/46 | chr2 | 53921194 | |||||||
chr2:53921270 | G | A | 248 | a0001c0001t0001g0173 a0001c0001t0003g0203 a0001c0005t0001g0182 others(245): Show |
248 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.2047-166C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 17/46 | chr2 | 53921270 | |||||||
chr2:53921491 | C | T | 1 | a0001c0001t0001g0001 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.2047-387G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 17/46 | chr2 | 53921491 | |||||||
chr2:53921574 | G | C | 58 | a0001c0005t0001g0182 a0001c0005t0001g0311 a0001c0005t0001g0313 others(55): Show |
58 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.2047-470C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 17/46 | chr2 | 53921574 | |||||||
chr2:53921595 | G | A | 64 | a0002c0002t0002g0022 a0002c0002t0002g0023 a0002c0002t0002g0043 others(61): Show |
64 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.2047-491C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 17/46 | chr2 | 53921595 | |||||||
chr2:53921628 | G | T | 1 | a0001c0001t0001g0215 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2047-524C>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 17/46 | chr2 | 53921628 | |||||||
chr2:53921640 | G | A | 3 | a0001c0007t0001g0015 a0001c0007t0001g0017 a0001c0007t0001g0179 |
3 | HG01081.hp2 HG02451.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.2047-536C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 17/46 | chr2 | 53921640 | |||||||
chr2:53921644 | G | A | 2 | a0001c0001t0001g0272 a0001c0001t0001g0273 |
2 | HG00323.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.2047-540C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 17/46 | chr2 | 53921644 | |||||||
chr2:53921676 | G | A | 1 | a0002c0003t0002g0077 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2047-572C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 17/46 | chr2 | 53921676 | |||||||
chr2:53921677 | G | A | 137 | a0002c0002t0002g0022 a0002c0002t0002g0023 a0002c0002t0002g0043 others(134): Show |
137 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.2047-573C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 17/46 | chr2 | 53921677 | |||||||
chr2:53921683 | A | T | 4 | a0001c0005t0001g0320 a0001c0005t0001g0324 a0001c0005t0001g0332 others(1): Show |
4 | HG00621.hp1 HG02132.hp2 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.2047-579T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 17/46 | chr2 | 53921683 | |||||||
chr2:53921699 | T | A | 2 | a0002c0002t0002g0063 a0002c0002t0002g0094 |
2 | NA18954.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.2047-595A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 17/46 | chr2 | 53921699 | |||||||
chr2:53921753 | A | G | 1 | a0002c0003t0002g0132 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2047-649T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 17/46 | chr2 | 53921753 | |||||||
chr2:53921783 | G | C | 70 | a0002c0003t0001g0079 a0002c0003t0002g0011 a0002c0003t0002g0016 others(67): Show |
70 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.2047-679C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 17/46 | chr2 | 53921783 | |||||||
chr2:53921842 | T | C | 1 | a0001c0009t0013g0292 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2046+675A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 17/46 | chr2 | 53921842 | |||||||
chr2:53921854 | C | G | 58 | a0001c0005t0001g0182 a0001c0005t0001g0311 a0001c0005t0001g0313 others(55): Show |
58 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.2046+663G>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 17/46 | chr2 | 53921854 | |||||||
chr2:53921867 | C | CAAAAAAA others(4): Show |
3 | a0002c0002t0002g0094 a0002c0002t0004g0064 a0002c0003t0002g0149 |
3 | HG01256.hp2 NA19056.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.2046+649_2046+650i others(13): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 17/46 | chr2 | 53921867 | |||||||
chr2:53921867 | C | CAAAAAAA others(5): Show |
130 | a0002c0002t0002g0022 a0002c0002t0002g0023 a0002c0002t0002g0043 others(127): Show |
130 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.2046+649_2046+650i others(14): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 17/46 | chr2 | 53921867 | |||||||
chr2:53921867 | C | CAAAAAAA others(6): Show |
4 | a0002c0002t0002g0096 a0002c0002t0002g0154 a0002c0003t0004g0340 others(1): Show |
4 | HG02602.hp1 HG03831.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.2046+649_2046+650i others(15): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 17/46 | chr2 | 53921867 | |||||||
chr2:53921949 | G | A | 3 | a0001c0007t0001g0015 a0001c0007t0001g0017 a0001c0007t0001g0179 |
3 | HG01081.hp2 HG02451.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.2046+568C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 17/46 | chr2 | 53921949 | |||||||
chr2:53922022 | A | G | 1 | a0003c0004t0001g0303 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2046+495T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 17/46 | chr2 | 53922022 | |||||||
chr2:53922055 | C | A | 3 | a0002c0010t0002g0018 a0002c0010t0002g0051 a0002c0010t0002g0056 |
3 | HG02572.hp1 HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2046+462G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 17/46 | chr2 | 53922055 | |||||||
chr2:53922108 | T | C | 66 | a0002c0003t0001g0079 a0002c0003t0002g0011 a0002c0003t0002g0016 others(63): Show |
66 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.2046+409A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 17/46 | chr2 | 53922108 | |||||||
chr2:53922131 | C | A | 4 | a0001c0005t0001g0320 a0001c0005t0001g0324 a0001c0005t0001g0332 others(1): Show |
4 | HG00621.hp1 HG02132.hp2 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.2046+386G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 17/46 | chr2 | 53922131 | |||||||
chr2:53922172 | A | AAAAAG | 4 | a0001c0001t0003g0203 a0001c0006t0005g0003 a0001c0006t0005g0005 others(1): Show |
4 | HG02109.hp1 HG02976.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.2046+340_2046+344d others(7): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 17/46 | chr2 | 53922172 | |||||||
chr2:53922235 | A | G | 1 | a0001c0009t0013g0292 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2046+282T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 17/46 | chr2 | 53922235 | |||||||
chr2:53922248 | T | G | 139 | a0001c0022t0016g0111 a0002c0002t0002g0022 a0002c0002t0002g0023 others(136): Show |
139 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.2046+269A>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 17/46 | chr2 | 53922248 | |||||||
chr2:53922486 | T | C | 1 | a0001c0001t0001g0281 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2046+31A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 17/46 | chr2 | 53922486 | |||||||
chr2:53922729 | C | T | 1 | a0001c0001t0003g0203 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1979-145G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 16/46 | chr2 | 53922729 | |||||||
chr2:53922805 | TC | T | 44 | a0001c0001t0001g0173 a0001c0006t0003g0025 a0001c0006t0003g0026 others(41): Show |
44 | HG00099.hp2 HG00738.hp2 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.1979-222delG | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 16/46 | chr2 | 53922805 | |||||||
chr2:53922868 | A | C | 2 | a0001c0005t0001g0372 a0001c0005t0001g0373 |
2 | HG00408.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.1978+181T>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 16/46 | chr2 | 53922868 | |||||||
chr2:53922897 | G | A | 2 | a0001c0006t0003g0031 a0001c0006t0003g0177 |
2 | HG02970.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1978+152C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 16/46 | chr2 | 53922897 | |||||||
chr2:53922942 | A | T | 64 | a0002c0002t0002g0022 a0002c0002t0002g0023 a0002c0002t0002g0043 others(61): Show |
64 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.1978+107T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 16/46 | chr2 | 53922942 | |||||||
chr2:53922969 | T | C | 1 | a0004c0008t0001g0382 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1978+80A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 16/46 | chr2 | 53922969 | |||||||
chr2:53923214 | A | T | 3 | a0002c0002t0002g0087 a0002c0002t0002g0088 a0002c0002t0002g0121 |
3 | HG02622.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1909-96T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 15/46 | chr2 | 53923214 | |||||||
chr2:53923281 | G | A | 1 | a0001c0018t0001g0229 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1908+40C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 15/46 | chr2 | 53923281 | |||||||
chr2:53923293 | A | G | 3 | a0003c0004t0001g0183 a0003c0004t0001g0195 a0003c0004t0001g0261 |
3 | HG00558.hp2 NA18747.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1908+28T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 15/46 | chr2 | 53923293 | |||||||
chr2:53923301 | G | C | 1 | a0001c0009t0001g0365 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1908+20C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 15/46 | chr2 | 53923301 | |||||||
chr2:53923549 | G | A | 6 | a0001c0001t0001g0053 a0001c0001t0001g0181 a0001c0001t0001g0191 others(3): Show |
6 | HG01255.hp2 HG02976.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1810-130C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 14/46 | chr2 | 53923549 | |||||||
chr2:53923723 | G | C | 2 | a0001c0001t0001g0272 a0001c0001t0001g0273 |
2 | HG00323.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.1810-304C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 14/46 | chr2 | 53923723 | |||||||
chr2:53923867 | G | A | 135 | a0001c0022t0016g0111 a0002c0002t0002g0022 a0002c0002t0002g0023 others(132): Show |
135 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.1810-448C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 14/46 | chr2 | 53923867 | |||||||
chr2:53923913 | C | CA | 69 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0001t0001g0180 others(66): Show |
70 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.1810-495dupT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 14/46 | chr2 | 53923913 | |||||||
chr2:53923913 | C | CAA | 21 | a0001c0001t0001g0038 a0001c0001t0001g0214 a0001c0006t0003g0030 others(18): Show |
21 | HG00438.hp2 HG00735.hp2 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.1810-496_1810-495d others(4): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 14/46 | chr2 | 53923913 | |||||||
chr2:53923913 | CAAAAAAA others(2): Show |
C | 31 | a0001c0005t0001g0182 a0001c0005t0001g0311 a0001c0005t0001g0316 others(28): Show |
31 | HG00597.hp1 HG01081.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.1810-503_1810-495d others(11): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 14/46 | chr2 | 53923913 | |||||||
chr2:53923913 | CAAAAAAA others(3): Show |
C | 26 | a0001c0005t0001g0313 a0001c0005t0001g0314 a0001c0005t0001g0315 others(23): Show |
26 | HG00408.hp1 HG00423.hp1 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.1810-504_1810-495d others(12): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 14/46 | chr2 | 53923913 | |||||||
chr2:53923913 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0185 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1810-505_1810-495d others(13): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 14/46 | chr2 | 53923913 | |||||||
chr2:53923913 | CAAAAAAA others(5): Show |
C | 7 | a0001c0007t0001g0361 a0001c0007t0006g0012 a0001c0007t0006g0014 others(4): Show |
7 | HG02559.hp2 HG02965.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.1810-506_1810-495d others(14): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 14/46 | chr2 | 53923913 | |||||||
chr2:53923913 | CAAAAAAA others(10): Show |
C | 69 | a0001c0009t0013g0292 a0002c0002t0002g0022 a0002c0002t0002g0023 others(66): Show |
69 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.1810-511_1810-495d others(19): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 14/46 | chr2 | 53923913 | |||||||
chr2:53923913 | CAAAAAAA others(11): Show |
C | 71 | a0001c0022t0016g0111 a0002c0003t0001g0079 a0002c0003t0002g0011 others(68): Show |
71 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.1810-512_1810-495d others(20): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 14/46 | chr2 | 53923913 | |||||||
chr2:53923925 | A | C | 2 | a0001c0005t0001g0372 a0001c0005t0001g0373 |
2 | HG00408.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.1810-506T>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 14/46 | chr2 | 53923925 | |||||||
chr2:53924037 | T | C | 5 | a0002c0003t0002g0049 a0002c0003t0002g0055 a0002c0003t0002g0058 others(2): Show |
5 | HG02809.hp1 HG02970.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1810-618A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 14/46 | chr2 | 53924037 | |||||||
chr2:53924395 | A | G | 3 | a0002c0002t0002g0116 a0002c0002t0002g0117 a0002c0002t0002g0140 |
3 | HG02027.hp1 NA18990.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.1810-976T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 14/46 | chr2 | 53924395 | |||||||
chr2:53924540 | A | C | 4 | a0002c0003t0002g0070 a0002c0003t0002g0071 a0002c0003t0002g0080 others(1): Show |
4 | NA18970.hp1 NA18984.hp1 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.1809+999T>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 14/46 | chr2 | 53924540 | |||||||
chr2:53924551 | G | T | 1 | a0004c0008t0001g0376 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1809+988C>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 14/46 | chr2 | 53924551 | |||||||
chr2:53924570 | A | G | 1 | a0002c0002t0002g0086 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1809+969T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 14/46 | chr2 | 53924570 | |||||||
chr2:53924649 | G | A | 1 | a0002c0002t0002g0086 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1809+890C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 14/46 | chr2 | 53924649 | |||||||
chr2:53924791 | T | C | 6 | a0001c0006t0003g0025 a0001c0006t0003g0026 a0001c0006t0003g0027 others(3): Show |
6 | HG01099.hp2 HG01106.hp1 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.1809+748A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 14/46 | chr2 | 53924791 | |||||||
chr2:53924976 | T | C | 1 | a0001c0009t0001g0365 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1809+563A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 14/46 | chr2 | 53924976 | |||||||
chr2:53925281 | T | C | 1 | a0001c0001t0001g0232 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1809+258A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 14/46 | chr2 | 53925281 | |||||||
chr2:53925305 | T | C | 3 | a0001c0006t0003g0026 a0001c0006t0003g0027 a0001c0006t0003g0030 |
3 | HG01099.hp2 HG01106.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.1809+234A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 14/46 | chr2 | 53925305 | |||||||
chr2:53925361 | C | T | 1 | a0001c0006t0003g0159 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1809+178G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 14/46 | chr2 | 53925361 | |||||||
chr2:53925392 | T | G | 3 | a0001c0007t0001g0015 a0001c0007t0001g0017 a0001c0007t0001g0179 |
3 | HG01081.hp2 HG02451.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.1809+147A>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 14/46 | chr2 | 53925392 | |||||||
chr2:53925426 | T | C | 2 | a0001c0005t0009g0220 a0001c0005t0009g0221 |
2 | NA18968.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.1809+113A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 14/46 | chr2 | 53925426 | |||||||
chr2:53925448 | C | T | 2 | a0002c0003t0002g0060 a0002c0003t0002g0078 |
2 | HG03239.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.1809+91G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 14/46 | chr2 | 53925448 | |||||||
chr2:53925468 | T | C | 1 | a0001c0001t0001g0001 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1809+71A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 14/46 | chr2 | 53925468 | |||||||
chr2:53925790 | T | C | 140 | a0001c0001t0001g0228 a0001c0022t0016g0111 a0002c0002t0002g0022 others(137): Show |
140 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.1659-101A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 13/46 | chr2 | 53925790 | |||||||
chr2:53925822 | G | C | 1 | a0001c0005t0001g0373 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1659-133C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 13/46 | chr2 | 53925822 | |||||||
chr2:53925843 | G | A | 8 | a0002c0002t0002g0050 a0002c0002t0002g0084 a0002c0002t0002g0093 others(5): Show |
8 | HG00423.hp2 HG02015.hp1 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.1658+116C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 13/46 | chr2 | 53925843 | |||||||
chr2:53926044 | G | C | 6 | a0001c0001t0001g0053 a0001c0001t0001g0181 a0001c0001t0001g0191 others(3): Show |
6 | HG01255.hp2 HG02976.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1594-21C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 12/46 | chr2 | 53926044 | |||||||
chr2:53926147 | A | G | 5 | a0001c0001t0001g0035 a0001c0001t0001g0223 a0001c0001t0001g0233 others(2): Show |
5 | HG00280.hp1 HG01070.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.1594-124T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 12/46 | chr2 | 53926147 | |||||||
chr2:53926193 | A | G | 2 | a0002c0010t0002g0018 a0002c0010t0002g0056 |
2 | HG02572.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1594-170T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 12/46 | chr2 | 53926193 | |||||||
chr2:53926204 | T | C | 72 | a0001c0001t0001g0228 a0001c0022t0016g0111 a0002c0003t0001g0079 others(69): Show |
72 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.1594-181A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 12/46 | chr2 | 53926204 | |||||||
chr2:53926230 | A | T | 3 | a0001c0005t0001g0316 a0001c0005t0001g0318 a0001c0005t0001g0353 |
3 | HG01515.hp2 HG01517.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1594-207T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 12/46 | chr2 | 53926230 | |||||||
chr2:53926402 | T | TG | 45 | a0001c0001t0001g0173 a0001c0006t0003g0025 a0001c0006t0003g0026 others(42): Show |
45 | HG00099.hp2 HG00738.hp2 HG01074.hp1 others(42): Show |
intron_variant | MODIFIER | c.1594-380dupC | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 12/46 | chr2 | 53926402 | |||||||
chr2:53926416 | G | A | 13 | a0001c0001t0001g0180 a0001c0001t0001g0198 a0001c0001t0001g0199 others(10): Show |
13 | HG02486.hp2 HG02630.hp1 HG02896.hp1 others(10): Show |
intron_variant | MODIFIER | c.1594-393C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 12/46 | chr2 | 53926416 | |||||||
chr2:53926440 | G | A | 1 | a0002c0010t0002g0056 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1594-417C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 12/46 | chr2 | 53926440 | |||||||
chr2:53926545 | T | G | 140 | a0001c0001t0001g0228 a0001c0022t0016g0111 a0002c0002t0002g0022 others(137): Show |
140 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.1594-522A>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 12/46 | chr2 | 53926545 | |||||||
chr2:53926705 | G | A | 9 | a0001c0001t0001g0036 a0001c0001t0001g0189 a0001c0001t0001g0190 others(6): Show |
9 | HG00733.hp1 HG01261.hp2 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.1594-682C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 12/46 | chr2 | 53926705 | |||||||
chr2:53926707 | C | T | 140 | a0001c0001t0001g0228 a0001c0022t0016g0111 a0002c0002t0002g0022 others(137): Show |
140 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.1594-684G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 12/46 | chr2 | 53926707 | |||||||
chr2:53926716 | G | A | 2 | a0003c0004t0001g0192 a0003c0004t0001g0245 |
2 | HG02622.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1593+678C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 12/46 | chr2 | 53926716 | |||||||
chr2:53926743 | C | T | 42 | a0001c0001t0001g0173 a0001c0006t0003g0025 a0001c0006t0003g0026 others(39): Show |
42 | HG00099.hp2 HG00738.hp2 HG01074.hp1 others(39): Show |
intron_variant | MODIFIER | c.1593+651G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 12/46 | chr2 | 53926743 | |||||||
chr2:53926770 | C | T | 1 | a0014c0026t0001g0013 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1593+624G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 12/46 | chr2 | 53926770 | |||||||
chr2:53926835 | A | G | 140 | a0001c0001t0001g0228 a0001c0022t0016g0111 a0002c0002t0002g0022 others(137): Show |
140 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.1593+559T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 12/46 | chr2 | 53926835 | |||||||
chr2:53926923 | A | C | 1 | a0002c0003t0002g0049 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1593+471T>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 12/46 | chr2 | 53926923 | |||||||
chr2:53926979 | A | C | 1 | a0001c0009t0001g0370 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1593+415T>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 12/46 | chr2 | 53926979 | |||||||
chr2:53926982 | AG | A | 137 | a0001c0001t0001g0228 a0001c0022t0016g0111 a0002c0002t0002g0022 others(134): Show |
137 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.1593+411delC | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 12/46 | chr2 | 53926982 | |||||||
chr2:53926983 | G | A | 2 | a0002c0003t0002g0136 a0002c0003t0002g0150 |
2 | HG01123.hp2 HG01257.hp2 |
intron_variant | MODIFIER | c.1593+411C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 12/46 | chr2 | 53926983 | |||||||
chr2:53927038 | AAAATCTT others(8): Show |
A | 2 | a0003c0004t0001g0192 a0003c0004t0001g0245 |
2 | HG02622.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1593+341_1593+355d others(17): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 12/46 | chr2 | 53927038 | |||||||
chr2:53927043 | C | T | 1 | a0002c0003t0002g0066 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1593+351G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 12/46 | chr2 | 53927043 | |||||||
chr2:53927050 | C | A | 3 | a0002c0010t0002g0018 a0002c0010t0002g0051 a0002c0010t0002g0056 |
3 | HG02572.hp1 HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1593+344G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 12/46 | chr2 | 53927050 | |||||||
chr2:53927097 | T | C | 1 | a0002c0002t0002g0154 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1593+297A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 12/46 | chr2 | 53927097 | |||||||
chr2:53927118 | T | C | 3 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0270 |
3 | HG03209.hp2 NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1593+276A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 12/46 | chr2 | 53927118 | |||||||
chr2:53927575 | T | C | 1 | a0001c0001t0001g0188 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1504-92A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 11/46 | chr2 | 53927575 | |||||||
chr2:53927793 | G | A | 2 | a0001c0007t0006g0012 a0001c0007t0006g0014 |
2 | HG02559.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1504-310C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 11/46 | chr2 | 53927793 | |||||||
chr2:53927906 | C | T | 1 | a0002c0003t0002g0020 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1503+211G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 11/46 | chr2 | 53927906 | |||||||
chr2:53928051 | T | TGTGACTG others(7): Show |
6 | a0002c0002t0002g0050 a0002c0002t0002g0084 a0002c0002t0002g0093 others(3): Show |
6 | HG00423.hp2 HG02083.hp1 HG02129.hp2 others(3): Show |
intron_variant | MODIFIER | c.1503+65_1503+66ins others(14): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 11/46 | chr2 | 53928051 | |||||||
chr2:53928052 | T | A | 6 | a0002c0002t0002g0050 a0002c0002t0002g0084 a0002c0002t0002g0093 others(3): Show |
6 | HG00423.hp2 HG02083.hp1 HG02129.hp2 others(3): Show |
intron_variant | MODIFIER | c.1503+65A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 11/46 | chr2 | 53928052 | |||||||
chr2:53928103 | A | G | 142 | a0001c0001t0001g0228 a0001c0005t0001g0323 a0001c0022t0016g0111 others(139): Show |
142 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.1503+14T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 11/46 | chr2 | 53928103 | |||||||
chr2:53928520 | T | TCA | 243 | a0001c0001t0001g0173 a0001c0001t0001g0228 a0001c0005t0001g0182 others(240): Show |
243 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(240): Show |
intron_variant | MODIFIER | c.1317-218_1317-217i others(4): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 10/46 | chr2 | 53928520 | |||||||
chr2:53928901 | C | G | 2 | a0001c0006t0005g0003 a0001c0006t0005g0005 |
2 | HG02109.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1317-598G>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 10/46 | chr2 | 53928901 | |||||||
chr2:53928958 | G | A | 13 | a0003c0004t0001g0040 a0003c0004t0001g0257 a0003c0004t0001g0274 others(10): Show |
13 | HG02132.hp1 NA18959.hp2 NA18963.hp1 others(10): Show |
intron_variant | MODIFIER | c.1317-655C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 10/46 | chr2 | 53928958 | |||||||
chr2:53929038 | T | C | 1 | a0002c0003t0002g0133 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1317-735A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 10/46 | chr2 | 53929038 | |||||||
chr2:53929074 | G | C | 1 | a0002c0002t0002g0131 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1317-771C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 10/46 | chr2 | 53929074 | |||||||
chr2:53929165 | C | CA | 263 | a0001c0001t0001g0053 a0001c0001t0001g0173 a0001c0001t0001g0181 others(260): Show |
263 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(260): Show |
intron_variant | MODIFIER | c.1317-863dupT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 10/46 | chr2 | 53929165 | |||||||
chr2:53929186 | T | A | 1 | a0006c0012t0002g0057 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1317-883A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 10/46 | chr2 | 53929186 | |||||||
chr2:53929454 | G | A | 1 | a0002c0010t0002g0056 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1317-1151C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 10/46 | chr2 | 53929454 | |||||||
chr2:53929804 | G | A | 11 | a0001c0006t0003g0025 a0001c0006t0003g0026 a0001c0006t0003g0027 others(8): Show |
11 | HG00099.hp2 HG01099.hp2 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.1317-1501C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 10/46 | chr2 | 53929804 | |||||||
chr2:53930030 | TAATA | T | 4 | a0005c0011t0001g0362 a0005c0011t0001g0364 a0005c0011t0002g0363 others(1): Show |
4 | HG01243.hp1 HG01891.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1317-1731_1317-172 others(8): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 10/46 | chr2 | 53930030 | |||||||
chr2:53930131 | G | A | 2 | a0002c0003t0002g0104 a0002c0003t0002g0110 |
2 | HG00408.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.1316+1704C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 10/46 | chr2 | 53930131 | |||||||
chr2:53930148 | A | C | 1 | a0002c0002t0004g0064 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1316+1687T>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 10/46 | chr2 | 53930148 | |||||||
chr2:53930329 | A | G | 2 | a0002c0002t0002g0122 a0002c0002t0004g0123 |
2 | NA18975.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.1316+1506T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 10/46 | chr2 | 53930329 | |||||||
chr2:53930430 | G | A | 3 | a0001c0006t0003g0163 a0001c0006t0003g0165 a0001c0006t0003g0166 |
3 | NA18951.hp2 NA18973.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.1316+1405C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 10/46 | chr2 | 53930430 | |||||||
chr2:53930631 | G | C | 1 | a0002c0002t0002g0355 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1316+1204C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 10/46 | chr2 | 53930631 | |||||||
chr2:53930679 | C | G | 1 | a0002c0002t0002g0131 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1316+1156G>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 10/46 | chr2 | 53930679 | |||||||
chr2:53930688 | T | G | 1 | a0001c0009t0001g0370 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1316+1147A>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 10/46 | chr2 | 53930688 | |||||||
chr2:53930698 | G | C | 1 | a0002c0003t0002g0076 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1316+1137C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 10/46 | chr2 | 53930698 | |||||||
chr2:53930767 | G | A | 140 | a0001c0001t0001g0053 a0001c0001t0001g0228 a0001c0022t0016g0111 others(137): Show |
140 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.1316+1068C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 10/46 | chr2 | 53930767 | |||||||
chr2:53930830 | A | G | 1 | a0001c0001t0001g0236 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1316+1005T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 10/46 | chr2 | 53930830 | |||||||
chr2:53931105 | C | T | 1 | a0002c0003t0002g0049 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1316+730G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 10/46 | chr2 | 53931105 | |||||||
chr2:53931108 | T | C | 3 | a0001c0005t0001g0336 a0001c0005t0001g0341 a0001c0005t0001g0350 |
3 | NA18955.hp2 NA18986.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.1316+727A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 10/46 | chr2 | 53931108 | |||||||
chr2:53931214 | T | A | 3 | a0002c0010t0002g0018 a0002c0010t0002g0051 a0002c0010t0002g0056 |
3 | HG02572.hp1 HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1316+621A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 10/46 | chr2 | 53931214 | |||||||
chr2:53931330 | C | G | 1 | a0002c0015t0002g0359 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1316+505G>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 10/46 | chr2 | 53931330 | |||||||
chr2:53931429 | A | G | 2 | a0001c0006t0005g0003 a0001c0006t0005g0005 |
2 | HG02109.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1316+406T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 10/46 | chr2 | 53931429 | |||||||
chr2:53931548 | G | A | 1 | a0001c0001t0001g0267 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1316+287C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 10/46 | chr2 | 53931548 | |||||||
chr2:53931707 | C | T | 1 | a0001c0007t0001g0179 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1316+128G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 10/46 | chr2 | 53931707 | |||||||
chr2:53931820 | C | T | 138 | a0001c0001t0001g0053 a0001c0001t0001g0228 a0001c0022t0016g0111 others(135): Show |
138 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.1316+15G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 10/46 | chr2 | 53931820 | |||||||
chr2:53932174 | T | A | 3 | a0001c0007t0001g0015 a0001c0007t0001g0017 a0001c0007t0001g0179 |
3 | HG01081.hp2 HG02451.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.1051-74A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 9/46 | chr2 | 53932174 | |||||||
chr2:53932196 | A | G | 1 | a0002c0015t0002g0359 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1051-96T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 9/46 | chr2 | 53932196 | |||||||
chr2:53932335 | T | A | 1 | a0002c0003t0002g0011 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1051-235A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 9/46 | chr2 | 53932335 | |||||||
chr2:53932477 | T | A | 6 | a0003c0004t0001g0040 a0003c0004t0001g0257 a0003c0004t0001g0274 others(3): Show |
6 | NA18959.hp2 NA18969.hp2 NA18978.hp2 others(3): Show |
intron_variant | MODIFIER | c.1050+191A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 9/46 | chr2 | 53932477 | |||||||
chr2:53932635 | C | T | 2 | a0002c0003t0002g0112 a0002c0003t0002g0133 |
2 | HG01175.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.1050+33G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 9/46 | chr2 | 53932635 | |||||||
chr2:53932770 | T | C | 1 | a0002c0002t0002g0124 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.958-10A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53932770 | |||||||
chr2:53932850 | A | G | 1 | a0002c0003t0002g0069 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.958-90T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53932850 | |||||||
chr2:53932862 | G | A | 99 | a0001c0001t0001g0173 a0001c0005t0001g0311 a0001c0005t0001g0313 others(96): Show |
99 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.958-102C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53932862 | |||||||
chr2:53932922 | T | C | 55 | a0001c0005t0001g0311 a0001c0005t0001g0313 a0001c0005t0001g0314 others(52): Show |
55 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.958-162A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53932922 | |||||||
chr2:53933024 | A | G | 1 | a0014c0026t0001g0013 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.958-264T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933024 | |||||||
chr2:53933145 | A | G | 101 | a0001c0001t0001g0173 a0001c0005t0001g0311 a0001c0005t0001g0313 others(98): Show |
101 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.958-385T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933145 | |||||||
chr2:53933303 | G | A | 9 | a0002c0003t0002g0024 a0002c0003t0002g0136 a0002c0003t0002g0144 others(6): Show |
9 | HG00733.hp2 HG01123.hp2 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.958-543C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933303 | |||||||
chr2:53933308 | G | A | 44 | a0001c0001t0001g0173 a0001c0006t0003g0025 a0001c0006t0003g0026 others(41): Show |
44 | HG00099.hp2 HG00738.hp2 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.958-548C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933308 | |||||||
chr2:53933375 | C | CA | 12 | a0001c0001t0001g0038 a0001c0001t0001g0188 a0001c0001t0001g0205 others(9): Show |
12 | HG00597.hp2 HG01346.hp1 HG01358.hp2 others(9): Show |
intron_variant | MODIFIER | c.958-616dupT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933375 | |||||||
chr2:53933375 | C | CAAA | 10 | a0001c0001t0001g0180 a0001c0001t0001g0199 a0001c0001t0001g0204 others(7): Show |
10 | HG01243.hp2 HG02896.hp1 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.958-618_958-616dup others(3): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933375 | |||||||
chr2:53933375 | C | CAAAAAAA | 9 | a0001c0001t0001g0267 a0001c0006t0003g0163 a0001c0006t0003g0167 others(6): Show |
9 | HG01109.hp1 HG01884.hp1 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.958-622_958-616dup others(7): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933375 | |||||||
chr2:53933375 | C | CAAAAAAA others(1): Show |
13 | a0001c0001t0001g0173 a0001c0006t0003g0025 a0001c0006t0003g0026 others(10): Show |
13 | HG01074.hp1 HG01081.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.958-623_958-616dup others(8): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933375 | |||||||
chr2:53933375 | C | CAAAAAAA others(2): Show |
23 | a0001c0001t0001g0191 a0001c0006t0003g0030 a0001c0006t0003g0031 others(20): Show |
23 | HG00099.hp2 HG00558.hp2 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.958-624_958-616dup others(9): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933375 | |||||||
chr2:53933375 | C | CAAAAAAA others(3): Show |
6 | a0001c0006t0003g0155 a0001c0006t0003g0157 a0001c0009t0001g0369 others(3): Show |
6 | HG01891.hp1 HG02004.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.958-625_958-616dup others(10): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933375 | |||||||
chr2:53933375 | C | CAAAAAAA others(4): Show |
4 | a0001c0001t0001g0240 a0001c0006t0003g0172 a0001c0007t0006g0014 others(1): Show |
4 | HG02257.hp2 HG03209.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.958-626_958-616dup others(11): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933375 | |||||||
chr2:53933375 | C | CAAAAAAA others(5): Show |
5 | a0001c0001t0001g0181 a0001c0001t0001g0239 a0001c0007t0001g0361 others(2): Show |
5 | HG01255.hp2 HG02559.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.958-627_958-616dup others(12): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933375 | |||||||
chr2:53933375 | C | CAAAAAAA others(6): Show |
11 | a0003c0004t0001g0039 a0003c0004t0001g0193 a0003c0004t0001g0200 others(8): Show |
11 | HG01884.hp2 HG02622.hp2 NA18952.hp1 others(8): Show |
intron_variant | MODIFIER | c.958-628_958-616dup others(13): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933375 | |||||||
chr2:53933375 | C | CAAAAAAA others(7): Show |
8 | a0003c0004t0001g0042 a0003c0004t0001g0192 a0003c0004t0001g0250 others(5): Show |
8 | HG02280.hp1 HG02572.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.958-629_958-616dup others(14): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933375 | |||||||
chr2:53933375 | C | CAAAAAAA others(8): Show |
5 | a0003c0004t0001g0040 a0003c0004t0001g0254 a0003c0004t0001g0257 others(2): Show |
5 | HG02109.hp2 NA18959.hp2 NA18969.hp2 others(2): Show |
intron_variant | MODIFIER | c.958-630_958-616dup others(15): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933375 | |||||||
chr2:53933375 | C | CAAAAAAA others(9): Show |
1 | a0003c0004t0001g0306 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.958-631_958-616dup others(16): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933375 | |||||||
chr2:53933375 | C | CAAAAAAA others(11): Show |
1 | a0003c0004t0001g0271 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.958-633_958-616dup others(18): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933375 | |||||||
chr2:53933375 | C | CAAAAAAA others(13): Show |
1 | a0003c0004t0001g0302 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.958-635_958-616dup others(20): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933375 | |||||||
chr2:53933375 | C | CAAAAAAA others(14): Show |
4 | a0003c0004t0001g0033 a0003c0004t0001g0256 a0003c0004t0001g0301 others(1): Show |
4 | HG02027.hp2 HG02523.hp1 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.958-636_958-616dup others(21): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933375 | |||||||
chr2:53933375 | C | CAAAAAAA others(15): Show |
1 | a0003c0004t0001g0303 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.958-637_958-616dup others(22): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933375 | |||||||
chr2:53933375 | C | CAAAAAAA others(17): Show |
3 | a0001c0001t0001g0241 a0003c0004t0001g0195 a0003c0004t0001g0286 |
3 | HG03225.hp1 NA18747.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.958-639_958-616dup others(24): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933375 | |||||||
chr2:53933375 | C | CAAAAAAA others(18): Show |
3 | a0003c0004t0001g0248 a0003c0004t0001g0298 a0003c0004t0001g0300 |
3 | HG02015.hp2 HG02132.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.958-640_958-616dup others(25): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933375 | |||||||
chr2:53933375 | C | CAAAAAAA others(19): Show |
1 | a0003c0004t0001g0289 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.958-641_958-616dup others(26): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933375 | |||||||
chr2:53933375 | C | CAAAAAAA others(21): Show |
1 | a0003c0004t0001g0247 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.958-643_958-616dup others(28): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933375 | |||||||
chr2:53933375 | C | CAAAAAAA others(25): Show |
1 | a0003c0004t0001g0258 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.958-616_958-615ins others(32): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933375 | |||||||
chr2:53933375 | C | CAAAAAAA others(28): Show |
1 | a0008c0025t0001g0259 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.958-616_958-615ins others(35): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933375 | |||||||
chr2:53933375 | C | CAAAAAAA others(32): Show |
1 | a0003c0004t0001g0290 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.958-616_958-615ins others(39): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933375 | |||||||
chr2:53933375 | C | CAAAAAAA others(33): Show |
1 | a0003c0004t0001g0261 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.958-616_958-615ins others(40): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933375 | |||||||
chr2:53933375 | CA | C | 23 | a0001c0001t0001g0036 a0001c0001t0001g0189 a0001c0001t0001g0224 others(20): Show |
23 | HG00423.hp1 HG00733.hp1 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.958-616delT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933375 | |||||||
chr2:53933375 | CAA | C | 39 | a0001c0005t0001g0315 a0001c0005t0001g0316 a0001c0005t0001g0318 others(36): Show |
39 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.958-617_958-616del others(2): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933375 | |||||||
chr2:53933375 | CAAAAAAA others(2): Show |
C | 15 | a0002c0002t0002g0047 a0002c0002t0002g0097 a0002c0002t0002g0098 others(12): Show |
15 | HG03831.hp2 HG04199.hp2 HG04228.hp2 others(12): Show |
intron_variant | MODIFIER | c.958-624_958-616del others(9): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933375 | |||||||
chr2:53933375 | CAAAAAAA others(3): Show |
C | 131 | a0001c0001t0001g0053 a0001c0001t0001g0228 a0001c0022t0016g0111 others(128): Show |
131 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.958-625_958-616del others(10): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933375 | |||||||
chr2:53933375 | CAAAAAAA others(4): Show |
C | 3 | a0001c0006t0005g0002 a0001c0006t0005g0004 a0002c0003t0002g0149 |
3 | HG01256.hp2 HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.958-626_958-616del others(11): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933375 | |||||||
chr2:53933375 | CAAAAAAA others(5): Show |
C | 1 | a0014c0026t0001g0013 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.958-627_958-616del others(12): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933375 | |||||||
chr2:53933443 | A | T | 60 | a0001c0001t0001g0053 a0001c0001t0001g0228 a0001c0022t0016g0111 others(57): Show |
60 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.958-683T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933443 | |||||||
chr2:53933541 | G | A | 4 | a0001c0007t0006g0012 a0001c0007t0006g0014 a0001c0007t0006g0196 others(1): Show |
4 | HG02559.hp2 HG02965.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.958-781C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933541 | |||||||
chr2:53933630 | T | C | 141 | a0001c0001t0001g0053 a0001c0001t0001g0228 a0001c0022t0016g0111 others(138): Show |
141 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.958-870A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933630 | |||||||
chr2:53933681 | C | T | 139 | a0001c0001t0001g0053 a0001c0001t0001g0228 a0001c0022t0016g0111 others(136): Show |
139 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.958-921G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933681 | |||||||
chr2:53933686 | T | C | 56 | a0001c0005t0001g0311 a0001c0005t0001g0313 a0001c0005t0001g0314 others(53): Show |
56 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.957+919A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933686 | |||||||
chr2:53933912 | G | C | 3 | a0001c0007t0001g0015 a0001c0007t0001g0017 a0001c0007t0001g0179 |
3 | HG01081.hp2 HG02451.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.957+693C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933912 | |||||||
chr2:53933913 | G | T | 140 | a0001c0001t0001g0053 a0001c0001t0001g0228 a0001c0022t0016g0111 others(137): Show |
140 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.957+692C>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933913 | |||||||
chr2:53933922 | A | T | 4 | a0001c0005t0001g0320 a0001c0005t0001g0324 a0001c0005t0001g0332 others(1): Show |
4 | HG00621.hp1 HG02132.hp2 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.957+683T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933922 | |||||||
chr2:53933972 | A | C | 11 | a0001c0006t0003g0025 a0001c0006t0003g0026 a0001c0006t0003g0027 others(8): Show |
11 | HG00099.hp2 HG01099.hp2 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.957+633T>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53933972 | |||||||
chr2:53934061 | A | G | 3 | a0002c0002t0002g0356 a0002c0002t0002g0358 a0016c0024t0001g0312 |
3 | HG02615.hp2 HG03195.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.957+544T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53934061 | |||||||
chr2:53934226 | T | C | 43 | a0001c0001t0001g0173 a0001c0006t0003g0025 a0001c0006t0003g0026 others(40): Show |
43 | HG00099.hp2 HG00738.hp2 HG01074.hp1 others(40): Show |
intron_variant | MODIFIER | c.957+379A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53934226 | |||||||
chr2:53934307 | G | T | 1 | a0003c0004t0001g0207 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.957+298C>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53934307 | |||||||
chr2:53934368 | T | C | 1 | a0003c0004t0001g0269 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.957+237A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 8/46 | chr2 | 53934368 | |||||||
chr2:53934748 | G | T | 137 | a0001c0001t0001g0053 a0001c0001t0001g0228 a0001c0022t0016g0111 others(134): Show |
137 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.835-21C>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 7/46 | chr2 | 53934748 | |||||||
chr2:53934795 | C | T | 1 | a0001c0005t0001g0313 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.835-68G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 7/46 | chr2 | 53934795 | |||||||
chr2:53934829 | T | C | 1 | a0001c0001t0007g0222 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.835-102A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 7/46 | chr2 | 53934829 | |||||||
chr2:53934875 | C | T | 1 | a0002c0015t0002g0359 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.835-148G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 7/46 | chr2 | 53934875 | |||||||
chr2:53934885 | C | T | 239 | a0001c0001t0001g0053 a0001c0001t0001g0173 a0001c0001t0001g0228 others(236): Show |
239 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.835-158G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 7/46 | chr2 | 53934885 | |||||||
chr2:53934939 | G | C | 44 | a0001c0001t0001g0173 a0001c0006t0003g0025 a0001c0006t0003g0026 others(41): Show |
44 | HG00099.hp2 HG00738.hp2 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.835-212C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 7/46 | chr2 | 53934939 | |||||||
chr2:53935003 | G | C | 1 | a0001c0001t0001g0010 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.835-276C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 7/46 | chr2 | 53935003 | |||||||
chr2:53935088 | T | TCCTGAGC others(3): Show |
1 | a0002c0003t0002g0019 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.835-371_835-362dup others(10): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 7/46 | chr2 | 53935088 | |||||||
chr2:53935226 | T | C | 1 | a0001c0009t0001g0365 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.835-499A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 7/46 | chr2 | 53935226 | |||||||
chr2:53935317 | A | T | 252 | a0001c0001t0001g0053 a0001c0001t0001g0173 a0001c0001t0001g0228 others(249): Show |
252 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(249): Show |
intron_variant | MODIFIER | c.835-590T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 7/46 | chr2 | 53935317 | |||||||
chr2:53935324 | G | C | 1 | a0001c0006t0003g0371 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.835-597C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 7/46 | chr2 | 53935324 | |||||||
chr2:53935358 | C | A | 1 | a0003c0004t0001g0201 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.835-631G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 7/46 | chr2 | 53935358 | |||||||
chr2:53935718 | T | C | 4 | a0001c0001t0001g0035 a0001c0001t0001g0223 a0001c0001t0001g0233 others(1): Show |
4 | HG00280.hp1 HG01070.hp1 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.834+369A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 7/46 | chr2 | 53935718 | |||||||
chr2:53935874 | G | A | 3 | a0001c0007t0001g0015 a0001c0007t0001g0017 a0001c0007t0001g0179 |
3 | HG01081.hp2 HG02451.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.834+213C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 7/46 | chr2 | 53935874 | |||||||
chr2:53935897 | G | GT | 57 | a0001c0005t0001g0313 a0001c0005t0001g0314 a0001c0005t0001g0315 others(54): Show |
57 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.834+189dupA | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 7/46 | chr2 | 53935897 | |||||||
chr2:53936036 | G | A | 2 | a0002c0002t0002g0100 a0002c0002t0002g0126 |
2 | NA19011.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.834+51C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 7/46 | chr2 | 53936036 | |||||||
chr2:53936212 | A | T | 1 | a0002c0003t0002g0128 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.760-51T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 6/46 | chr2 | 53936212 | |||||||
chr2:53936382 | A | G | 1 | a0002c0003t0002g0076 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.760-221T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 6/46 | chr2 | 53936382 | |||||||
chr2:53936587 | C | CAAATA | 141 | a0001c0001t0001g0053 a0001c0001t0001g0228 a0001c0022t0016g0111 others(138): Show |
141 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.759+172_759+176dup others(5): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 6/46 | chr2 | 53936587 | |||||||
chr2:53936709 | G | A | 2 | a0002c0003t0002g0136 a0002c0003t0002g0150 |
2 | HG01123.hp2 HG01257.hp2 |
intron_variant | MODIFIER | c.759+55C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 6/46 | chr2 | 53936709 | |||||||
chr2:53936747 | G | C | 1 | a0001c0022t0016g0111 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.759+17C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 6/46 | chr2 | 53936747 | |||||||
chr2:53936931 | C | T | 2 | a0002c0003t0002g0077 a0002c0003t0002g0108 |
2 | HG01106.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.696-104G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 5/46 | chr2 | 53936931 | |||||||
chr2:53937169 | T | C | 1 | a0017c0014t0002g0067 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.695+222A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 5/46 | chr2 | 53937169 | |||||||
chr2:53937236 | G | A | 39 | a0001c0001t0001g0173 a0001c0006t0003g0025 a0001c0006t0003g0026 others(36): Show |
39 | HG00099.hp2 HG00738.hp2 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.695+155C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 5/46 | chr2 | 53937236 | |||||||
chr2:53937382 | C | T | 2 | a0001c0006t0005g0002 a0001c0006t0005g0004 |
2 | HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.695+9G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 5/46 | chr2 | 53937382 | |||||||
chr2:53937645 | T | C | 1 | a0001c0005t0001g0343 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.546-105A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 4/46 | chr2 | 53937645 | |||||||
chr2:53937711 | G | T | 196 | a0001c0001t0001g0053 a0001c0001t0001g0228 a0001c0005t0001g0311 others(193): Show |
196 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.546-171C>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 4/46 | chr2 | 53937711 | |||||||
chr2:53937724 | G | A | 1 | a0002c0010t0002g0051 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.546-184C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 4/46 | chr2 | 53937724 | |||||||
chr2:53937925 | G | A | 1 | a0001c0001t0001g0236 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.546-385C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 4/46 | chr2 | 53937925 | |||||||
chr2:53938163 | C | G | 1 | a0001c0007t0001g0179 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.546-623G>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 4/46 | chr2 | 53938163 | |||||||
chr2:53938474 | C | CT | 7 | a0001c0001t0001g0180 a0001c0001t0001g0212 a0001c0001t0001g0214 others(4): Show |
7 | HG00735.hp1 HG02257.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.546-935dupA | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 4/46 | chr2 | 53938474 | |||||||
chr2:53938474 | CT | C | 12 | a0001c0006t0003g0156 a0001c0007t0001g0179 a0002c0002t0002g0045 others(9): Show |
12 | HG01167.hp2 HG02451.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.546-935delA | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 4/46 | chr2 | 53938474 | |||||||
chr2:53938510 | G | C | 1 | a0001c0001t0001g0208 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.546-970C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 4/46 | chr2 | 53938510 | |||||||
chr2:53938546 | G | C | 1 | a0004c0008t0001g0382 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.546-1006C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 4/46 | chr2 | 53938546 | |||||||
chr2:53938572 | G | A | 1 | a0001c0001t0001g0282 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.546-1032C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 4/46 | chr2 | 53938572 | |||||||
chr2:53938635 | A | G | 103 | a0001c0001t0001g0173 a0001c0005t0001g0311 a0001c0005t0001g0313 others(100): Show |
103 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.546-1095T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 4/46 | chr2 | 53938635 | |||||||
chr2:53938709 | G | T | 235 | a0001c0001t0001g0053 a0001c0001t0001g0173 a0001c0001t0001g0228 others(232): Show |
235 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.546-1169C>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 4/46 | chr2 | 53938709 | |||||||
chr2:53938769 | C | A | 3 | a0001c0007t0001g0015 a0001c0007t0001g0017 a0001c0007t0001g0179 |
3 | HG01081.hp2 HG02451.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.545+1187G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 4/46 | chr2 | 53938769 | |||||||
chr2:53938795 | T | G | 1 | a0001c0001t0001g0001 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.545+1161A>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 4/46 | chr2 | 53938795 | |||||||
chr2:53938832 | T | C | 7 | a0001c0007t0001g0015 a0001c0007t0001g0017 a0001c0007t0001g0179 others(4): Show |
7 | HG01081.hp2 HG01243.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.545+1124A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 4/46 | chr2 | 53938832 | |||||||
chr2:53938846 | G | C | 5 | a0001c0007t0006g0012 a0001c0007t0006g0014 a0001c0007t0006g0196 others(2): Show |
5 | HG02559.hp2 HG02965.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.545+1110C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 4/46 | chr2 | 53938846 | |||||||
chr2:53938855 | G | A | 132 | a0001c0001t0001g0053 a0001c0001t0001g0228 a0001c0022t0016g0111 others(129): Show |
132 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.545+1101C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 4/46 | chr2 | 53938855 | |||||||
chr2:53939045 | A | C | 2 | a0001c0006t0005g0002 a0001c0006t0005g0004 |
2 | HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.545+911T>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 4/46 | chr2 | 53939045 | |||||||
chr2:53939184 | C | T | 56 | a0001c0005t0001g0311 a0001c0005t0001g0313 a0001c0005t0001g0314 others(53): Show |
56 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.545+772G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 4/46 | chr2 | 53939184 | |||||||
chr2:53939206 | C | T | 1 | a0001c0001t0001g0267 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.545+750G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 4/46 | chr2 | 53939206 | |||||||
chr2:53939265 | C | A | 1 | a0001c0001t0001g0282 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.545+691G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 4/46 | chr2 | 53939265 | |||||||
chr2:53939488 | G | A | 1 | a0001c0001t0001g0053 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.545+468C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 4/46 | chr2 | 53939488 | |||||||
chr2:53939526 | G | A | 64 | a0002c0002t0002g0022 a0002c0002t0002g0023 a0002c0002t0002g0043 others(61): Show |
64 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.545+430C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 4/46 | chr2 | 53939526 | |||||||
chr2:53939534 | C | T | 3 | a0002c0003t0002g0077 a0002c0003t0002g0108 a0009c0031t0002g0021 |
3 | HG01106.hp2 HG01261.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.545+422G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 4/46 | chr2 | 53939534 | |||||||
chr2:53939616 | G | A | 1 | a0001c0001t0001g0240 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.545+340C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 4/46 | chr2 | 53939616 | |||||||
chr2:53939663 | A | G | 3 | a0002c0003t0002g0077 a0002c0003t0002g0108 a0009c0031t0002g0021 |
3 | HG01106.hp2 HG01261.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.545+293T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 4/46 | chr2 | 53939663 | |||||||
chr2:53939756 | G | A | 1 | a0013c0030t0002g0310 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.545+200C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 4/46 | chr2 | 53939756 | |||||||
chr2:53940091 | C | T | 3 | a0001c0001t0001g0180 a0001c0001t0001g0214 a0001c0001t0001g0215 |
3 | HG02630.hp1 HG03130.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.501-91G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940091 | |||||||
chr2:53940461 | T | C | 2 | a0001c0006t0005g0003 a0001c0006t0005g0005 |
2 | HG02109.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.501-461A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940461 | |||||||
chr2:53940467 | C | T | 3 | a0002c0010t0002g0018 a0002c0010t0002g0051 a0002c0010t0002g0056 |
3 | HG02572.hp1 HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.501-467G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940467 | |||||||
chr2:53940636 | T | C | 12 | a0002c0002t0002g0023 a0002c0002t0002g0043 a0002c0002t0002g0054 others(9): Show |
12 | HG00280.hp2 HG00323.hp1 HG02155.hp1 others(9): Show |
intron_variant | MODIFIER | c.501-636A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940636 | |||||||
chr2:53940672 | G | A | 69 | a0001c0001t0001g0053 a0001c0001t0001g0228 a0001c0022t0016g0111 others(66): Show |
69 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.501-672C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940672 | |||||||
chr2:53940832 | C | T | 3 | a0001c0007t0001g0015 a0001c0007t0001g0017 a0001c0007t0001g0179 |
3 | HG01081.hp2 HG02451.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.501-832G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940832 | |||||||
chr2:53940862 | T | A | 1 | a0001c0019t0001g0037 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.501-862A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940862 | |||||||
chr2:53940865 | T | C | 2 | a0007c0013t0002g0046 a0007c0013t0002g0073 |
2 | NA19002.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.501-865A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940865 | |||||||
chr2:53940867 | T | C | 239 | a0001c0001t0001g0053 a0001c0001t0001g0173 a0001c0001t0001g0228 others(236): Show |
239 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.501-867A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940867 | |||||||
chr2:53940875 | A | AATATATA others(39): Show |
19 | a0002c0002t0002g0054 a0002c0002t0002g0063 a0002c0002t0002g0085 others(16): Show |
19 | HG00621.hp2 HG02027.hp1 HG02155.hp1 others(16): Show |
intron_variant | MODIFIER | c.501-921_501-876dup others(46): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940875 | |||||||
chr2:53940875 | A | AATATATA others(58): Show |
1 | a0002c0003t0002g0055 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.501-876_501-875ins others(65): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940875 | |||||||
chr2:53940875 | A | AATATATA others(60): Show |
11 | a0001c0001t0001g0053 a0002c0003t0002g0011 a0002c0003t0002g0052 others(8): Show |
11 | HG02809.hp1 HG02818.hp2 HG03041.hp1 others(8): Show |
intron_variant | MODIFIER | c.501-876_501-875ins others(67): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940875 | |||||||
chr2:53940875 | A | AATATATA others(129): Show |
1 | a0002c0003t0002g0019 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.501-876_501-875ins others(136): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940875 | |||||||
chr2:53940896 | A | AATATATA others(171): Show |
1 | a0002c0003t0002g0078 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.501-897_501-896ins others(178): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940896 | |||||||
chr2:53940896 | A | AATATATA others(127): Show |
2 | a0002c0003t0002g0112 a0002c0003t0002g0133 |
2 | HG01175.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.501-897_501-896ins others(134): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940896 | |||||||
chr2:53940896 | A | AATATATA others(83): Show |
2 | a0002c0003t0002g0070 a0017c0014t0002g0067 |
2 | NA18984.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.501-897_501-896ins others(90): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940896 | |||||||
chr2:53940896 | A | AATATATA others(129): Show |
1 | a0002c0003t0002g0106 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.501-897_501-896ins others(136): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940896 | |||||||
chr2:53940896 | A | AATATATA others(150): Show |
1 | a0002c0021t0002g0113 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.501-897_501-896ins others(157): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940896 | |||||||
chr2:53940896 | A | AATATATA others(131): Show |
1 | a0002c0003t0002g0104 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.501-897_501-896ins others(138): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940896 | |||||||
chr2:53940896 | AATATATA others(16): Show |
A | 4 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(1): Show |
4 | HG00738.hp1 HG01123.hp1 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.501-919_501-897del others(23): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940896 | |||||||
chr2:53940914 | T | A | 3 | a0001c0001t0001g0184 a0001c0001t0001g0212 a0001c0001t0001g0213 |
3 | HG01361.hp2 HG01952.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.501-914A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940914 | |||||||
chr2:53940917 | A | AAT | 155 | a0001c0001t0001g0173 a0001c0001t0001g0180 a0001c0001t0001g0181 others(152): Show |
155 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.501-919_501-918dup others(2): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940917 | |||||||
chr2:53940917 | A | AATATATA others(62): Show |
4 | a0002c0003t0002g0024 a0002c0003t0002g0136 a0002c0003t0002g0146 others(1): Show |
4 | HG01123.hp2 HG01168.hp2 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.501-918_501-917ins others(69): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940917 | |||||||
chr2:53940917 | AAT | A | 47 | a0001c0001t0001g0228 a0001c0006t0003g0155 a0001c0006t0003g0156 others(44): Show |
47 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.501-919_501-918del others(2): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940917 | |||||||
chr2:53940917 | AATATATA others(30): Show |
A | 3 | a0005c0011t0001g0362 a0005c0011t0001g0364 a0005c0011t0002g0363 |
3 | HG01243.hp1 HG01891.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.501-954_501-918del others(37): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940917 | |||||||
chr2:53940919 | T | TATATATA others(37): Show |
4 | a0002c0003t0002g0020 a0002c0003t0002g0077 a0002c0003t0002g0108 others(1): Show |
4 | HG01106.hp2 HG01192.hp2 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.501-920_501-919ins others(44): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940919 | |||||||
chr2:53940919 | T | TATATATA others(101): Show |
1 | a0002c0002t0002g0357 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.501-920_501-919ins others(108): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940919 | |||||||
chr2:53940921 | TATATATA others(24): Show |
T | 1 | a0001c0006t0003g0160 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.501-952_501-922del others(31): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940921 | |||||||
chr2:53940923 | TATATAAT others(10): Show |
T | 2 | a0001c0001t0001g0204 a0001c0001t0001g0238 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.501-940_501-924del others(17): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940923 | |||||||
chr2:53940927 | TAATACAT others(6): Show |
T | 1 | a0001c0001t0001g0212 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.501-940_501-928del others(13): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940927 | |||||||
chr2:53940928 | A | AT | 8 | a0002c0003t0002g0070 a0002c0003t0002g0078 a0002c0003t0002g0104 others(5): Show |
8 | HG01175.hp1 HG01943.hp2 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.501-929_501-928ins others(1): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940928 | |||||||
chr2:53940928 | A | ATAATACA others(61): Show |
2 | a0002c0002t0002g0097 a0002c0002t0002g0131 |
2 | HG02698.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.501-929_501-928ins others(68): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940928 | |||||||
chr2:53940932 | C | CATATTTA others(102): Show |
1 | a0002c0003t0002g0145 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.501-933_501-932ins others(109): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940932 | |||||||
chr2:53940934 | T | TATTTAAA others(92): Show |
1 | a0002c0003t0002g0080 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.501-935_501-934ins others(99): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940934 | |||||||
chr2:53940936 | T | TTTAA | 4 | a0001c0001t0001g0053 a0002c0003t0002g0019 a0002c0003t0002g0136 others(1): Show |
4 | HG01168.hp2 HG01257.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.501-937_501-936ins others(4): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940936 | |||||||
chr2:53940936 | T | TTTAAATA others(92): Show |
1 | a0002c0003t0002g0066 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.501-937_501-936ins others(99): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940936 | |||||||
chr2:53940936 | TATAAATA others(9): Show |
T | 1 | a0001c0001t0001g0184 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.501-952_501-937del others(16): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940936 | |||||||
chr2:53940937 | A | T | 113 | a0001c0001t0001g0213 a0001c0001t0001g0228 a0001c0006t0003g0155 others(110): Show |
113 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.501-937T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940937 | |||||||
chr2:53940938 | TAAATATA others(7): Show |
T | 1 | a0001c0001t0001g0213 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.501-952_501-939del others(14): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940938 | |||||||
chr2:53940940 | A | AAT | 16 | a0002c0002t0002g0054 a0002c0002t0002g0063 a0002c0002t0002g0085 others(13): Show |
16 | HG02027.hp1 HG02155.hp1 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.501-942_501-941dup others(2): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940940 | |||||||
chr2:53940940 | A | AATATATA others(88): Show |
1 | a0002c0003t0002g0076 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.501-941_501-940ins others(95): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940940 | |||||||
chr2:53940940 | A | C | 2 | a0001c0006t0005g0002 a0001c0006t0005g0004 |
2 | HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.501-940T>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940940 | |||||||
chr2:53940940 | A | T | 7 | a0001c0001t0001g0053 a0002c0003t0002g0019 a0002c0003t0002g0066 others(4): Show |
7 | HG00733.hp2 HG01168.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.501-940T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940940 | |||||||
chr2:53940940 | AATATATA others(9): Show |
A | 1 | a0013c0030t0002g0310 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.501-956_501-941del others(16): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940940 | |||||||
chr2:53940940 | AATATATA others(15): Show |
A | 2 | a0001c0005t0001g0314 a0001c0005t0009g0221 |
2 | NA18971.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.501-962_501-941del others(22): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940940 | |||||||
chr2:53940940 | AATATATA others(17): Show |
A | 55 | a0001c0005t0001g0311 a0001c0005t0001g0313 a0001c0005t0001g0315 others(52): Show |
55 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.501-964_501-941del others(24): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940940 | |||||||
chr2:53940942 | T | C | 1 | a0001c0001t0001g0212 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.501-942A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940942 | |||||||
chr2:53940942 | T | TATATATA others(57): Show |
7 | a0002c0002t0002g0047 a0002c0002t0002g0082 a0002c0002t0002g0092 others(4): Show |
7 | HG02040.hp2 HG02523.hp2 NA18612.hp1 others(4): Show |
intron_variant | MODIFIER | c.501-943_501-942ins others(64): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940942 | |||||||
chr2:53940942 | TATATATA others(3): Show |
T | 21 | a0001c0001t0001g0173 a0001c0006t0003g0025 a0001c0006t0003g0026 others(18): Show |
21 | HG01074.hp1 HG01099.hp2 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.501-952_501-943del others(10): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940942 | |||||||
chr2:53940944 | T | TATATAAT others(166): Show |
1 | a0001c0022t0016g0111 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.501-945_501-944ins others(173): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940944 | |||||||
chr2:53940944 | T | TATATAAT others(78): Show |
1 | a0002c0003t0002g0016 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.501-945_501-944ins others(85): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940944 | |||||||
chr2:53940944 | T | TATATAAT others(170): Show |
1 | a0002c0003t0002g0060 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.501-945_501-944ins others(177): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940944 | |||||||
chr2:53940944 | T | TATATAAT others(172): Show |
1 | a0002c0003t0002g0152 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.501-945_501-944ins others(179): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940944 | |||||||
chr2:53940944 | T | TATATAAT others(55): Show |
6 | a0002c0002t0002g0065 a0002c0002t0002g0068 a0002c0002t0002g0091 others(3): Show |
6 | NA18971.hp1 NA18986.hp1 NA18989.hp2 others(3): Show |
intron_variant | MODIFIER | c.501-945_501-944ins others(62): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940944 | |||||||
chr2:53940944 | T | TATATAAT others(151): Show |
1 | a0002c0003t0002g0299 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.501-945_501-944ins others(158): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940944 | |||||||
chr2:53940944 | T | TATATATA others(82): Show |
1 | a0002c0003t0002g0071 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.501-945_501-944ins others(89): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940944 | |||||||
chr2:53940944 | TATATATA others(1): Show |
T | 5 | a0001c0006t0005g0003 a0001c0006t0005g0005 a0001c0006t0014g0164 others(2): Show |
5 | HG00099.hp2 HG02109.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.501-952_501-945del others(8): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940944 | |||||||
chr2:53940946 | T | TATAATAC others(53): Show |
1 | a0002c0002t0002g0044 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.501-947_501-946ins others(60): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940946 | |||||||
chr2:53940946 | T | TATATATA others(82): Show |
1 | a0001c0001t0001g0228 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.501-947_501-946ins others(89): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940946 | |||||||
chr2:53940946 | TATATAC | T | 3 | a0001c0006t0003g0172 a0001c0006t0003g0175 a0001c0006t0003g0266 |
3 | HG01884.hp1 HG02257.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.501-952_501-947del others(6): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940946 | |||||||
chr2:53940947 | A | T | 1 | a0001c0001t0001g0212 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.501-947T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940947 | |||||||
chr2:53940948 | T | TA | 14 | a0002c0002t0002g0022 a0002c0002t0002g0050 a0002c0002t0002g0084 others(11): Show |
14 | HG00423.hp2 HG01255.hp1 HG02083.hp1 others(11): Show |
intron_variant | MODIFIER | c.501-949dupT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940948 | |||||||
chr2:53940948 | T | TAATACAT others(17): Show |
2 | a0002c0002t0002g0043 a0002c0002t0002g0086 |
2 | HG02602.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.501-949_501-948ins others(24): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940948 | |||||||
chr2:53940948 | T | TAATACAT others(51): Show |
2 | a0002c0002t0002g0096 a0002c0002t0002g0143 |
2 | HG02056.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.501-949_501-948ins others(58): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940948 | |||||||
chr2:53940948 | T | TAATACAT others(166): Show |
1 | a0002c0003t0002g0069 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.501-949_501-948ins others(173): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940948 | |||||||
chr2:53940948 | T | TAATACAT others(145): Show |
1 | a0002c0003t0001g0079 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.501-949_501-948ins others(152): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940948 | |||||||
chr2:53940948 | T | TAATACAT others(147): Show |
1 | a0002c0003t0002g0132 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.501-949_501-948ins others(154): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940948 | |||||||
chr2:53940948 | T | TAATACAT others(147): Show |
1 | a0002c0003t0002g0109 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.501-949_501-948ins others(154): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940948 | |||||||
chr2:53940948 | T | TATA | 4 | a0002c0003t0002g0020 a0002c0003t0002g0077 a0002c0003t0002g0108 others(1): Show |
4 | HG01106.hp2 HG01192.hp2 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.501-951_501-949dup others(3): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940948 | |||||||
chr2:53940948 | T | TATATA | 5 | a0001c0006t0003g0155 a0001c0006t0003g0156 a0001c0006t0003g0157 others(2): Show |
5 | HG01167.hp2 HG02886.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.501-949_501-948ins others(5): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940948 | |||||||
chr2:53940948 | T | TATATAAT others(78): Show |
2 | a0002c0003t0002g0137 a0002c0003t0002g0144 |
2 | HG03710.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.501-949_501-948ins others(85): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940948 | |||||||
chr2:53940948 | T | TATATAAT others(124): Show |
1 | a0002c0003t0002g0110 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.501-949_501-948ins others(131): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940948 | |||||||
chr2:53940948 | T | TATATAAT others(84): Show |
1 | a0002c0033t0002g0375 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.501-949_501-948ins others(91): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940948 | |||||||
chr2:53940948 | TATAC | T | 8 | a0001c0006t0003g0161 a0001c0006t0003g0178 a0001c0006t0003g0371 others(5): Show |
8 | HG00738.hp2 HG02559.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.501-952_501-949del others(4): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940948 | |||||||
chr2:53940949 | A | AATACATA others(72): Show |
2 | a0002c0003t0002g0059 a0002c0003t0002g0072 |
2 | NA18995.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.501-950_501-949ins others(79): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940949 | |||||||
chr2:53940949 | A | AATACATA others(47): Show |
6 | a0002c0002t0002g0023 a0002c0002t0002g0081 a0002c0002t0002g0083 others(3): Show |
6 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(3): Show |
intron_variant | MODIFIER | c.501-950_501-949ins others(54): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940949 | |||||||
chr2:53940949 | A | AATACATA others(143): Show |
1 | a0002c0003t0002g0297 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.501-950_501-949ins others(150): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940949 | |||||||
chr2:53940949 | A | ATATAATA others(74): Show |
2 | a0002c0003t0002g0049 a0002c0003t0004g0340 |
2 | HG03041.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.501-950_501-949ins others(81): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940949 | |||||||
chr2:53940949 | A | ATATAATA others(76): Show |
2 | a0007c0013t0002g0046 a0007c0013t0002g0073 |
2 | NA19002.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.501-950_501-949ins others(83): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940949 | |||||||
chr2:53940949 | A | ATATAATA others(120): Show |
5 | a0002c0003t0002g0105 a0002c0003t0002g0134 a0002c0003t0002g0135 others(2): Show |
5 | HG00735.hp1 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.501-950_501-949ins others(127): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940949 | |||||||
chr2:53940949 | A | ATATATAA others(76): Show |
1 | a0002c0003t0002g0107 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.501-950_501-949ins others(83): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940949 | |||||||
chr2:53940950 | T | TATAATAC others(76): Show |
2 | a0002c0003t0002g0075 a0002c0003t0002g0114 |
2 | HG00558.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.501-951_501-950ins others(83): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940950 | |||||||
chr2:53940950 | T | TATAATAC others(78): Show |
2 | a0002c0003t0002g0128 a0006c0012t0002g0057 |
2 | HG02083.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.501-951_501-950ins others(85): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940950 | |||||||
chr2:53940950 | T | TATAATAC others(122): Show |
2 | a0002c0003t0002g0139 a0002c0003t0002g0148 |
2 | HG01928.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.501-951_501-950ins others(129): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940950 | |||||||
chr2:53940950 | T | TATAATAC others(76): Show |
1 | a0002c0003t0002g0149 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.501-951_501-950ins others(83): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940950 | |||||||
chr2:53940950 | T | TATAATAC others(82): Show |
1 | a0002c0003t0011g0009 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.501-951_501-950ins others(89): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940950 | |||||||
chr2:53940950 | TAC | T | 8 | a0001c0006t0003g0167 a0001c0006t0003g0168 a0001c0006t0003g0170 others(5): Show |
8 | HG02630.hp2 HG02896.hp2 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.501-952_501-951del others(2): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940950 | |||||||
chr2:53940952 | C | A | 19 | a0002c0002t0002g0023 a0002c0002t0002g0081 a0002c0002t0002g0083 others(16): Show |
19 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(16): Show |
intron_variant | MODIFIER | c.501-952G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940952 | |||||||
chr2:53940952 | C | CATATATA others(7): Show |
1 | a0001c0001t0001g0244 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.501-966_501-953dup others(14): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940952 | |||||||
chr2:53940952 | C | CATATTT | 14 | a0001c0001t0001g0190 a0001c0001t0001g0225 a0001c0001t0001g0226 others(11): Show |
14 | HG00438.hp2 HG00733.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.501-953_501-952ins others(6): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940952 | |||||||
chr2:53940952 | C | CATATTTA others(11): Show |
1 | a0001c0007t0001g0179 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.501-953_501-952ins others(18): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940952 | |||||||
chr2:53940952 | C | CATATTTA others(48): Show |
1 | a0002c0015t0002g0359 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.501-953_501-952ins others(55): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940952 | |||||||
chr2:53940952 | C | CATATTTA others(54): Show |
1 | a0002c0002t0002g0103 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.501-953_501-952ins others(61): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940952 | |||||||
chr2:53940952 | C | CATATTTA others(56): Show |
1 | a0002c0002t0002g0045 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.501-953_501-952ins others(63): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940952 | |||||||
chr2:53940952 | C | CATATTTA others(1): Show |
21 | a0001c0001t0001g0224 a0001c0001t0001g0227 a0001c0001t0001g0234 others(18): Show |
21 | HG00558.hp2 HG01346.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.501-953_501-952ins others(8): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940952 | |||||||
chr2:53940952 | C | CATATTTA others(3): Show |
3 | a0003c0004t0001g0252 a0003c0004t0001g0291 a0003c0004t0001g0303 |
3 | HG01884.hp2 NA18940.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.501-953_501-952ins others(10): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940952 | |||||||
chr2:53940952 | C | CATATTTA others(7): Show |
1 | a0003c0004t0001g0251 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.501-953_501-952ins others(14): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940952 | |||||||
chr2:53940952 | C | CATATTTA others(9): Show |
2 | a0001c0001t0001g0036 a0001c0001t0001g0189 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.501-953_501-952ins others(16): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940952 | |||||||
chr2:53940952 | C | CATATTTT others(7): Show |
1 | a0001c0001t0001g0211 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.501-953_501-952ins others(14): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940952 | |||||||
chr2:53940952 | C | T | 71 | a0001c0001t0001g0212 a0001c0001t0001g0228 a0001c0022t0016g0111 others(68): Show |
71 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.501-952G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940952 | |||||||
chr2:53940952 | CAT | C | 8 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0188 others(5): Show |
8 | HG00738.hp1 HG01358.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.501-954_501-953del others(2): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940952 | |||||||
chr2:53940952 | CATAT | C | 5 | a0001c0001t0001g0191 a0001c0001t0001g0198 a0001c0001t0001g0199 others(2): Show |
5 | HG02976.hp1 HG03209.hp2 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.501-956_501-953del others(4): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940952 | |||||||
chr2:53940952 | CATATAT | C | 3 | a0001c0001t0001g0181 a0001c0001t0001g0241 a0001c0009t0013g0292 |
3 | HG01255.hp2 HG03225.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.501-958_501-953del others(6): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940952 | |||||||
chr2:53940953 | A | ATATT | 18 | a0001c0001t0001g0223 a0001c0001t0001g0233 a0001c0001t0001g0277 others(15): Show |
18 | HG01070.hp1 HG01071.hp1 HG02004.hp2 others(15): Show |
intron_variant | MODIFIER | c.501-954_501-953ins others(4): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940953 | |||||||
chr2:53940953 | A | T | 1 | a0001c0001t0001g0184 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.501-953T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940953 | |||||||
chr2:53940954 | T | C | 8 | a0002c0002t0002g0140 a0002c0002t0002g0141 a0002c0002t0002g0142 others(5): Show |
8 | HG00621.hp2 HG01123.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.501-954A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940954 | |||||||
chr2:53940954 | T | TACATATT others(3): Show |
2 | a0002c0003t0002g0052 a0002c0003t0002g0061 |
2 | NA19070.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.501-955_501-954ins others(10): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940954 | |||||||
chr2:53940954 | T | TATACATA others(5): Show |
3 | a0002c0003t0002g0127 a0002c0003t0010g0006 a0006c0012t0002g0062 |
3 | HG02809.hp1 HG02818.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.501-955_501-954ins others(12): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940954 | |||||||
chr2:53940954 | T | TATTTAA | 5 | a0002c0002t0002g0085 a0002c0002t0002g0088 a0002c0002t0002g0121 others(2): Show |
5 | HG02895.hp2 HG02897.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.501-955_501-954ins others(6): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940954 | |||||||
chr2:53940954 | T | TATTTAAA others(44): Show |
1 | a0002c0002t0002g0084 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.501-955_501-954ins others(51): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940954 | |||||||
chr2:53940955 | A | ACATATT | 3 | a0002c0003t0002g0011 a0002c0003t0002g0024 a0002c0003t0002g0055 |
3 | HG02735.hp2 HG02970.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.501-956_501-955ins others(6): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940955 | |||||||
chr2:53940955 | A | ATT | 22 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0038 others(19): Show |
23 | HG00597.hp2 HG00609.hp2 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.501-956_501-955ins others(2): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940955 | |||||||
chr2:53940955 | A | ATTTAAAT others(40): Show |
1 | a0002c0002t0002g0153 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.501-956_501-955ins others(47): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940955 | |||||||
chr2:53940956 | T | C | 6 | a0001c0006t0003g0167 a0001c0006t0003g0168 a0001c0006t0003g0170 others(3): Show |
6 | HG02630.hp2 HG02896.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.501-956A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940956 | |||||||
chr2:53940956 | T | TTTAA | 13 | a0001c0001t0001g0053 a0001c0007t0001g0015 a0002c0002t0002g0022 others(10): Show |
13 | HG01081.hp2 HG01106.hp2 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.501-957_501-956ins others(4): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940956 | |||||||
chr2:53940956 | T | TTTAAATA others(42): Show |
8 | a0002c0002t0002g0050 a0002c0002t0002g0093 a0002c0002t0002g0102 others(5): Show |
8 | HG00423.hp2 HG02129.hp2 NA18945.hp2 others(5): Show |
intron_variant | MODIFIER | c.501-957_501-956ins others(49): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940956 | |||||||
chr2:53940957 | A | T | 35 | a0001c0001t0001g0035 a0001c0001t0001g0180 a0001c0001t0001g0187 others(32): Show |
35 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(32): Show |
intron_variant | MODIFIER | c.501-957T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940957 | |||||||
chr2:53940958 | T | A | 4 | a0002c0002t0002g0153 a0002c0003t0002g0011 a0002c0003t0002g0024 others(1): Show |
4 | HG02735.hp2 HG02970.hp1 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.501-958A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940958 | |||||||
chr2:53940958 | T | C | 9 | a0001c0006t0003g0161 a0001c0006t0003g0178 a0001c0006t0003g0371 others(6): Show |
9 | HG00738.hp2 HG02559.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.501-958A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940958 | |||||||
chr2:53940958 | T | TTTAA | 7 | a0002c0002t0002g0140 a0002c0002t0002g0141 a0002c0002t0002g0142 others(4): Show |
7 | HG00621.hp2 HG01123.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.501-959_501-958ins others(4): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940958 | |||||||
chr2:53940959 | A | T | 6 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0188 others(3): Show |
6 | HG00738.hp1 HG01358.hp2 HG02293.hp2 others(3): Show |
intron_variant | MODIFIER | c.501-959T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940959 | |||||||
chr2:53940960 | T | A | 22 | a0001c0001t0001g0204 a0001c0001t0001g0238 a0001c0006t0003g0155 others(19): Show |
22 | HG01167.hp2 HG01168.hp2 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.501-960A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940960 | |||||||
chr2:53940960 | T | C | 5 | a0001c0006t0003g0172 a0001c0006t0003g0175 a0001c0006t0003g0266 others(2): Show |
5 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.501-960A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940960 | |||||||
chr2:53940961 | A | T | 10 | a0001c0001t0001g0191 a0001c0001t0001g0198 a0001c0001t0001g0199 others(7): Show |
10 | HG02630.hp2 HG02896.hp2 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.501-961T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940961 | |||||||
chr2:53940962 | T | A | 1 | a0014c0026t0001g0013 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.501-962A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940962 | |||||||
chr2:53940962 | T | C | 5 | a0001c0006t0005g0003 a0001c0006t0005g0005 a0001c0006t0014g0164 others(2): Show |
5 | HG00099.hp2 HG02109.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.501-962A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940962 | |||||||
chr2:53940963 | A | T | 11 | a0001c0001t0001g0181 a0001c0001t0001g0241 a0001c0006t0003g0161 others(8): Show |
11 | HG00738.hp2 HG01255.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.501-963T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940963 | |||||||
chr2:53940964 | T | A | 6 | a0001c0006t0003g0167 a0001c0006t0003g0168 a0001c0006t0003g0170 others(3): Show |
6 | HG02630.hp2 HG02896.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.501-964A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940964 | |||||||
chr2:53940964 | T | C | 22 | a0001c0001t0001g0173 a0001c0006t0003g0025 a0001c0006t0003g0026 others(19): Show |
22 | HG01074.hp1 HG01099.hp2 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.501-964A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940964 | |||||||
chr2:53940965 | A | T | 6 | a0001c0001t0001g0239 a0001c0006t0003g0172 a0001c0006t0003g0175 others(3): Show |
6 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.501-965T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940965 | |||||||
chr2:53940966 | T | A | 9 | a0001c0006t0003g0161 a0001c0006t0003g0178 a0001c0006t0003g0371 others(6): Show |
9 | HG00738.hp2 HG02559.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.501-966A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940966 | |||||||
chr2:53940966 | T | TAATACAT others(41): Show |
1 | a0002c0002t0002g0022 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.501-967_501-966ins others(48): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940966 | |||||||
chr2:53940967 | A | T | 5 | a0001c0006t0005g0003 a0001c0006t0005g0005 a0001c0006t0014g0164 others(2): Show |
5 | HG00099.hp2 HG02109.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.501-967T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940967 | |||||||
chr2:53940968 | T | A | 5 | a0001c0006t0003g0172 a0001c0006t0003g0175 a0001c0006t0003g0266 others(2): Show |
5 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.501-968A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940968 | |||||||
chr2:53940968 | T | TATAATAC others(30): Show |
3 | a0002c0010t0002g0018 a0002c0010t0002g0051 a0002c0010t0002g0056 |
3 | HG02572.hp1 HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.501-969_501-968ins others(37): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940968 | |||||||
chr2:53940969 | A | T | 22 | a0001c0001t0001g0173 a0001c0006t0003g0025 a0001c0006t0003g0026 others(19): Show |
22 | HG01074.hp1 HG01099.hp2 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.501-969T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940969 | |||||||
chr2:53940969 | AT | A | 3 | a0005c0011t0001g0362 a0005c0011t0001g0364 a0005c0011t0002g0363 |
3 | HG01243.hp1 HG01891.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.501-970delA | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940969 | |||||||
chr2:53940970 | T | A | 5 | a0001c0006t0005g0003 a0001c0006t0005g0005 a0001c0006t0014g0164 others(2): Show |
5 | HG00099.hp2 HG02109.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.501-970A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940970 | |||||||
chr2:53940970 | T | C | 1 | a0013c0030t0002g0310 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.501-970A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940970 | |||||||
chr2:53940972 | T | A | 22 | a0001c0001t0001g0173 a0001c0006t0003g0025 a0001c0006t0003g0026 others(19): Show |
22 | HG01074.hp1 HG01099.hp2 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.501-972A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940972 | |||||||
chr2:53940972 | T | C | 6 | a0001c0001t0001g0204 a0001c0001t0001g0238 a0002c0003t0002g0020 others(3): Show |
6 | HG01106.hp2 HG01192.hp2 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.501-972A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940972 | |||||||
chr2:53940972 | T | TACATATT others(3): Show |
6 | a0001c0006t0003g0155 a0001c0006t0003g0156 a0001c0006t0003g0157 others(3): Show |
6 | HG01167.hp2 HG02602.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.501-973_501-972ins others(10): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940972 | |||||||
chr2:53940974 | T | A | 2 | a0002c0002t0002g0100 a0002c0002t0002g0126 |
2 | NA19011.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.501-974A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940974 | |||||||
chr2:53940974 | T | C | 4 | a0002c0002t0002g0043 a0005c0011t0001g0362 a0005c0011t0001g0364 others(1): Show |
4 | HG01243.hp1 HG01891.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.501-974A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940974 | |||||||
chr2:53940975 | A | T | 1 | a0013c0030t0002g0310 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.501-975T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940975 | |||||||
chr2:53940976 | T | C | 2 | a0001c0005t0001g0314 a0001c0005t0009g0221 |
2 | NA18971.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.501-976A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940976 | |||||||
chr2:53940977 | A | T | 6 | a0001c0001t0001g0204 a0001c0001t0001g0238 a0002c0003t0002g0020 others(3): Show |
6 | HG01106.hp2 HG01192.hp2 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.501-977T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940977 | |||||||
chr2:53940978 | T | A | 1 | a0013c0030t0002g0310 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.501-978A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940978 | |||||||
chr2:53940978 | T | C | 55 | a0001c0005t0001g0311 a0001c0005t0001g0313 a0001c0005t0001g0315 others(52): Show |
55 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.501-978A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940978 | |||||||
chr2:53940979 | A | T | 1 | a0002c0002t0002g0043 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.501-979T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940979 | |||||||
chr2:53940980 | T | A | 4 | a0002c0003t0002g0020 a0002c0003t0002g0077 a0002c0003t0002g0108 others(1): Show |
4 | HG01106.hp2 HG01192.hp2 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.501-980A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940980 | |||||||
chr2:53940981 | A | T | 2 | a0001c0005t0001g0314 a0001c0005t0009g0221 |
2 | NA18971.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.501-981T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940981 | |||||||
chr2:53940982 | T | A | 4 | a0002c0002t0002g0043 a0005c0011t0001g0362 a0005c0011t0001g0364 others(1): Show |
4 | HG01243.hp1 HG01891.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.501-982A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940982 | |||||||
chr2:53940983 | A | T | 55 | a0001c0005t0001g0311 a0001c0005t0001g0313 a0001c0005t0001g0315 others(52): Show |
55 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.501-983T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940983 | |||||||
chr2:53940986 | T | TACATATT others(3): Show |
2 | a0002c0002t0002g0100 a0002c0002t0002g0126 |
2 | NA19011.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.501-987_501-986ins others(10): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940986 | |||||||
chr2:53940994 | T | C | 7 | a0002c0002t0002g0044 a0002c0002t0002g0065 a0002c0002t0002g0098 others(4): Show |
7 | HG02056.hp1 NA18971.hp1 NA18978.hp1 others(4): Show |
intron_variant | MODIFIER | c.501-994A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940994 | |||||||
chr2:53940997 | A | G | 6 | a0002c0003t0002g0019 a0002c0003t0002g0069 a0002c0003t0002g0112 others(3): Show |
6 | HG00438.hp1 HG01175.hp1 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.501-997T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940997 | |||||||
chr2:53940998 | T | A | 6 | a0002c0003t0002g0019 a0002c0003t0002g0069 a0002c0003t0002g0112 others(3): Show |
6 | HG00438.hp1 HG01175.hp1 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.501-998A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940998 | |||||||
chr2:53940998 | T | TGA | 16 | a0001c0022t0016g0111 a0002c0003t0001g0079 a0002c0003t0002g0060 others(13): Show |
16 | HG00408.hp2 HG00735.hp1 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.501-999_501-998ins others(2): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940998 | |||||||
chr2:53940999 | A | G | 1 | a0002c0003t0002g0055 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.501-999T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53940999 | |||||||
chr2:53941098 | T | C | 1 | a0001c0001t0001g0267 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.501-1098A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53941098 | |||||||
chr2:53941175 | A | G | 136 | a0001c0001t0001g0053 a0001c0001t0001g0228 a0001c0022t0016g0111 others(133): Show |
136 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.501-1175T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53941175 | |||||||
chr2:53941354 | T | C | 1 | a0001c0001t0001g0215 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.501-1354A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53941354 | |||||||
chr2:53941468 | C | T | 1 | a0002c0002t0004g0118 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.501-1468G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53941468 | |||||||
chr2:53941477 | C | T | 2 | a0001c0006t0005g0002 a0001c0006t0005g0004 |
2 | HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.501-1477G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53941477 | |||||||
chr2:53941512 | G | C | 2 | a0001c0006t0005g0003 a0001c0006t0005g0005 |
2 | HG02109.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.501-1512C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53941512 | |||||||
chr2:53941744 | A | G | 54 | a0001c0001t0001g0173 a0001c0006t0003g0025 a0001c0006t0003g0026 others(51): Show |
54 | HG00099.hp2 HG00738.hp2 HG01074.hp1 others(51): Show |
intron_variant | MODIFIER | c.501-1744T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53941744 | |||||||
chr2:53941772 | A | G | 1 | a0002c0010t0002g0051 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.501-1772T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53941772 | |||||||
chr2:53941988 | G | A | 1 | a0002c0002t0002g0086 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.501-1988C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53941988 | |||||||
chr2:53942199 | C | G | 1 | a0002c0003t0002g0127 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.501-2199G>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53942199 | |||||||
chr2:53942253 | G | T | 1 | a0002c0002t0001g0235 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.501-2253C>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53942253 | |||||||
chr2:53942367 | G | GT | 6 | a0001c0001t0001g0211 a0002c0003t0002g0052 a0002c0003t0002g0075 others(3): Show |
6 | HG00558.hp1 HG02965.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.501-2368dupA | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53942367 | |||||||
chr2:53942379 | A | T | 89 | a0001c0001t0001g0053 a0001c0001t0001g0180 a0001c0001t0001g0198 others(86): Show |
89 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.501-2379T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53942379 | |||||||
chr2:53942483 | G | A | 1 | a0001c0007t0001g0361 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.501-2483C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53942483 | |||||||
chr2:53942567 | T | C | 7 | a0001c0001t0001g0181 a0001c0001t0001g0191 a0001c0001t0001g0216 others(4): Show |
7 | HG01255.hp2 HG02717.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.501-2567A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53942567 | |||||||
chr2:53942653 | G | A | 2 | a0001c0005t0001g0336 a0001c0005t0001g0350 |
2 | NA18955.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.501-2653C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53942653 | |||||||
chr2:53942812 | C | G | 4 | a0005c0011t0001g0362 a0005c0011t0001g0364 a0005c0011t0002g0363 others(1): Show |
4 | HG01243.hp1 HG01891.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.501-2812G>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53942812 | |||||||
chr2:53942898 | G | T | 134 | a0001c0001t0001g0053 a0001c0001t0001g0228 a0001c0022t0016g0111 others(131): Show |
134 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.501-2898C>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53942898 | |||||||
chr2:53943093 | T | C | 63 | a0002c0002t0002g0022 a0002c0002t0002g0023 a0002c0002t0002g0043 others(60): Show |
63 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.501-3093A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53943093 | |||||||
chr2:53943095 | T | C | 1 | a0001c0006t0003g0157 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.501-3095A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53943095 | |||||||
chr2:53943146 | G | A | 1 | a0001c0005t0001g0315 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.501-3146C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53943146 | |||||||
chr2:53943202 | A | G | 54 | a0001c0001t0001g0173 a0001c0006t0003g0025 a0001c0006t0003g0026 others(51): Show |
54 | HG00099.hp2 HG00738.hp2 HG01074.hp1 others(51): Show |
intron_variant | MODIFIER | c.501-3202T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53943202 | |||||||
chr2:53943295 | C | T | 2 | a0001c0005t0001g0315 a0001c0005t0001g0319 |
2 | HG01358.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.501-3295G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53943295 | |||||||
chr2:53943321 | T | A | 2 | a0001c0005t0001g0311 a0001c0005t0001g0337 |
2 | NA19000.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.501-3321A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53943321 | |||||||
chr2:53943333 | C | G | 251 | a0001c0001t0001g0053 a0001c0001t0001g0173 a0001c0001t0001g0228 others(248): Show |
251 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(248): Show |
intron_variant | MODIFIER | c.501-3333G>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53943333 | |||||||
chr2:53943359 | T | C | 6 | a0003c0004t0001g0042 a0003c0004t0001g0192 a0003c0004t0001g0245 others(3): Show |
6 | HG01884.hp2 HG02109.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.501-3359A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53943359 | |||||||
chr2:53943513 | C | G | 2 | a0001c0001t0001g0001 a0001c0019t0001g0037 |
3 | HG01168.hp1 HG01169.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.501-3513G>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53943513 | |||||||
chr2:53943750 | A | G | 249 | a0001c0001t0001g0053 a0001c0001t0001g0173 a0001c0001t0001g0228 others(246): Show |
249 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(246): Show |
intron_variant | MODIFIER | c.501-3750T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53943750 | |||||||
chr2:53943764 | C | T | 5 | a0002c0003t0002g0019 a0002c0003t0002g0069 a0002c0003t0002g0132 others(2): Show |
5 | HG00438.hp1 NA18948.hp1 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.501-3764G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53943764 | |||||||
chr2:53943846 | C | CA | 12 | a0001c0001t0001g0038 a0001c0005t0001g0311 a0001c0005t0001g0314 others(9): Show |
12 | HG02738.hp2 HG03831.hp2 NA18959.hp2 others(9): Show |
intron_variant | MODIFIER | c.501-3847dupT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53943846 | |||||||
chr2:53943846 | CA | C | 48 | a0001c0001t0001g0010 a0001c0001t0001g0173 a0001c0001t0001g0211 others(45): Show |
48 | HG00323.hp1 HG00621.hp1 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.501-3847delT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53943846 | |||||||
chr2:53943846 | CAAA | C | 67 | a0001c0001t0001g0228 a0001c0007t0001g0015 a0001c0007t0001g0017 others(64): Show |
67 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.501-3849_501-3847d others(5): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53943846 | |||||||
chr2:53943846 | CAAAA | C | 7 | a0001c0001t0001g0053 a0002c0003t0002g0049 a0002c0003t0002g0055 others(4): Show |
7 | HG01167.hp1 HG02809.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.501-3850_501-3847d others(6): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53943846 | |||||||
chr2:53943956 | G | T | 250 | a0001c0001t0001g0053 a0001c0001t0001g0173 a0001c0001t0001g0228 others(247): Show |
250 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(247): Show |
intron_variant | MODIFIER | c.501-3956C>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53943956 | |||||||
chr2:53944010 | C | T | 1 | a0005c0011t0001g0364 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.501-4010G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53944010 | |||||||
chr2:53944068 | T | G | 2 | a0003c0004t0001g0033 a0003c0004t0001g0256 |
2 | HG02027.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.501-4068A>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53944068 | |||||||
chr2:53944163 | AT | A | 7 | a0001c0005t0001g0338 a0001c0006t0005g0002 a0001c0006t0005g0004 others(4): Show |
7 | HG01243.hp1 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.501-4164delA | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53944163 | |||||||
chr2:53944388 | G | A | 1 | a0001c0001t0001g0278 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.500+4033C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53944388 | |||||||
chr2:53944516 | A | C | 2 | a0001c0006t0005g0002 a0001c0006t0005g0004 |
2 | HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.500+3905T>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53944516 | |||||||
chr2:53944530 | C | G | 1 | a0010c0027t0003g0162 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.500+3891G>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53944530 | |||||||
chr2:53944593 | T | C | 1 | a0001c0009t0001g0369 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.500+3828A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53944593 | |||||||
chr2:53944759 | T | C | 1 | a0001c0007t0006g0014 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.500+3662A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53944759 | |||||||
chr2:53945080 | T | C | 3 | a0002c0002t0002g0087 a0002c0002t0002g0088 a0002c0002t0002g0121 |
3 | HG02622.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.500+3341A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53945080 | |||||||
chr2:53945334 | G | A | 1 | a0005c0011t0002g0363 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.500+3087C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53945334 | |||||||
chr2:53945359 | C | G | 9 | a0001c0001t0001g0036 a0001c0001t0001g0189 a0001c0001t0001g0190 others(6): Show |
9 | HG00733.hp1 HG01261.hp2 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.500+3062G>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53945359 | |||||||
chr2:53945372 | ACTT | A | 3 | a0002c0010t0002g0018 a0002c0010t0002g0051 a0002c0010t0002g0056 |
3 | HG02572.hp1 HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.500+3046_500+3048d others(5): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53945372 | |||||||
chr2:53945512 | A | C | 1 | a0005c0011t0001g0362 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.500+2909T>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53945512 | |||||||
chr2:53945548 | G | T | 2 | a0007c0013t0002g0046 a0007c0013t0002g0073 |
2 | NA19002.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.500+2873C>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53945548 | |||||||
chr2:53945733 | T | C | 6 | a0002c0002t0002g0023 a0002c0002t0002g0063 a0002c0002t0002g0089 others(3): Show |
6 | NA18954.hp1 NA18975.hp1 NA18982.hp2 others(3): Show |
intron_variant | MODIFIER | c.500+2688A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53945733 | |||||||
chr2:53945754 | T | C | 1 | a0002c0003t0002g0055 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.500+2667A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53945754 | |||||||
chr2:53945755 | A | C | 1 | a0013c0030t0002g0310 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.500+2666T>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53945755 | |||||||
chr2:53945855 | T | G | 1 | a0001c0001t0001g0267 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.500+2566A>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53945855 | |||||||
chr2:53945930 | G | C | 60 | a0002c0002t0002g0022 a0002c0002t0002g0023 a0002c0002t0002g0043 others(57): Show |
60 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.500+2491C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53945930 | |||||||
chr2:53946087 | A | C | 2 | a0001c0006t0005g0003 a0001c0006t0005g0005 |
2 | HG02109.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.500+2334T>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53946087 | |||||||
chr2:53946396 | T | C | 2 | a0002c0003t0002g0134 a0002c0003t0002g0135 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.500+2025A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53946396 | |||||||
chr2:53946438 | G | C | 1 | a0002c0002t0001g0235 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.500+1983C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53946438 | |||||||
chr2:53946569 | T | A | 250 | a0001c0001t0001g0053 a0001c0001t0001g0173 a0001c0005t0001g0311 others(247): Show |
250 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(247): Show |
intron_variant | MODIFIER | c.500+1852A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53946569 | |||||||
chr2:53946866 | A | C | 1 | a0001c0009t0013g0292 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.500+1555T>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53946866 | |||||||
chr2:53946904 | C | A | 10 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0204 others(7): Show |
10 | HG01243.hp2 HG02486.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.500+1517G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53946904 | |||||||
chr2:53947121 | A | G | 56 | a0001c0005t0001g0311 a0001c0005t0001g0313 a0001c0005t0001g0314 others(53): Show |
56 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.500+1300T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53947121 | |||||||
chr2:53947248 | A | T | 1 | a0002c0002t0004g0048 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.500+1173T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53947248 | |||||||
chr2:53947290 | A | G | 3 | a0002c0002t0002g0116 a0002c0002t0002g0117 a0002c0002t0002g0140 |
3 | HG02027.hp1 NA18990.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.500+1131T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53947290 | |||||||
chr2:53947556 | A | G | 48 | a0001c0001t0001g0173 a0001c0006t0003g0025 a0001c0006t0003g0026 others(45): Show |
48 | HG00099.hp2 HG00738.hp2 HG01074.hp1 others(45): Show |
intron_variant | MODIFIER | c.500+865T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53947556 | |||||||
chr2:53947619 | C | T | 249 | a0001c0001t0001g0053 a0001c0001t0001g0173 a0001c0005t0001g0311 others(246): Show |
249 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(246): Show |
intron_variant | MODIFIER | c.500+802G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53947619 | |||||||
chr2:53947704 | T | TCAAAACA others(3): Show |
247 | a0001c0001t0001g0053 a0001c0001t0001g0173 a0001c0005t0001g0311 others(244): Show |
247 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(244): Show |
intron_variant | MODIFIER | c.500+707_500+716dup others(10): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53947704 | |||||||
chr2:53947711 | A | AAAACAAA others(3): Show |
2 | a0001c0007t0001g0361 a0016c0024t0001g0312 |
2 | HG03139.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.500+709_500+710ins others(10): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53947711 | |||||||
chr2:53947926 | G | A | 1 | a0002c0002t0002g0047 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.500+495C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53947926 | |||||||
chr2:53947992 | A | G | 2 | a0001c0006t0005g0002 a0001c0006t0005g0004 |
2 | HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.500+429T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53947992 | |||||||
chr2:53948303 | T | C | 24 | a0001c0022t0016g0111 a0002c0003t0001g0079 a0002c0003t0002g0019 others(21): Show |
24 | HG00408.hp2 HG00438.hp1 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.500+118A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53948303 | |||||||
chr2:53948309 | C | T | 5 | a0001c0001t0001g0181 a0001c0001t0001g0191 a0001c0001t0001g0239 others(2): Show |
5 | HG01255.hp2 HG02976.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.500+112G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53948309 | |||||||
chr2:53948369 | C | A | 2 | a0003c0004t0001g0032 a0003c0004t0001g0268 |
2 | NA18945.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.500+52G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53948369 | |||||||
chr2:53948380 | C | G | 1 | a0002c0002t0002g0151 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.500+41G>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53948380 | |||||||
chr2:53948383 | A | G | 1 | a0002c0003t0002g0072 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.500+38T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 3/46 | chr2 | 53948383 | |||||||
chr2:53948626 | T | C | 64 | a0002c0002t0002g0022 a0002c0002t0002g0023 a0002c0002t0002g0043 others(61): Show |
64 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.384-89A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 2/46 | chr2 | 53948626 | |||||||
chr2:53948652 | T | A | 1 | a0001c0009t0013g0292 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.384-115A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 2/46 | chr2 | 53948652 | |||||||
chr2:53948765 | T | C | 1 | a0002c0003t0002g0011 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.384-228A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 2/46 | chr2 | 53948765 | |||||||
chr2:53948768 | G | C | 68 | a0001c0001t0001g0053 a0001c0022t0016g0111 a0002c0003t0001g0079 others(65): Show |
68 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.384-231C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 2/46 | chr2 | 53948768 | |||||||
chr2:53948849 | CAGG | C | 4 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0001g0295 others(1): Show |
4 | HG00099.hp1 HG01081.hp1 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.383+291_383+293del others(3): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 2/46 | chr2 | 53948849 | |||||||
chr2:53949078 | C | A | 7 | a0001c0006t0005g0002 a0001c0006t0005g0004 a0003c0004t0003g0218 others(4): Show |
7 | HG01109.hp1 HG01243.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.383+65G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 2/46 | chr2 | 53949078 | |||||||
chr2:53949114 | T | C | 1 | a0017c0014t0002g0067 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.383+29A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 2/46 | chr2 | 53949114 | |||||||
chr2:53949321 | T | C | 1 | a0001c0001t0001g0010 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.243-38A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53949321 | |||||||
chr2:53949337 | T | C | 1 | a0001c0006t0005g0003 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.243-54A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53949337 | |||||||
chr2:53949356 | C | T | 1 | a0001c0005t0001g0317 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.243-73G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53949356 | |||||||
chr2:53949448 | C | CT | 58 | a0002c0002t0002g0022 a0002c0002t0002g0023 a0002c0002t0002g0043 others(55): Show |
58 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.243-166dupA | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53949448 | |||||||
chr2:53949448 | CT | C | 72 | a0001c0001t0001g0053 a0001c0005t0001g0313 a0001c0005t0001g0323 others(69): Show |
72 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.243-166delA | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53949448 | |||||||
chr2:53949490 | G | C | 1 | a0001c0001t0001g0236 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.243-207C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53949490 | |||||||
chr2:53949541 | A | G | 1 | a0010c0027t0003g0162 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.243-258T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53949541 | |||||||
chr2:53949596 | C | A | 3 | a0001c0007t0001g0015 a0001c0007t0001g0017 a0001c0007t0001g0179 |
3 | HG01081.hp2 HG02451.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.243-313G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53949596 | |||||||
chr2:53949740 | T | C | 1 | a0001c0009t0001g0360 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.243-457A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53949740 | |||||||
chr2:53949824 | T | C | 1 | a0002c0003t0002g0128 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.243-541A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53949824 | |||||||
chr2:53949979 | T | C | 1 | a0014c0026t0001g0013 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.243-696A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53949979 | |||||||
chr2:53949993 | G | T | 71 | a0001c0001t0001g0053 a0001c0022t0016g0111 a0002c0003t0001g0079 others(68): Show |
71 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.243-710C>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53949993 | |||||||
chr2:53949994 | G | A | 1 | a0002c0003t0002g0128 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.243-711C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53949994 | |||||||
chr2:53950055 | A | G | 131 | a0001c0001t0001g0053 a0001c0001t0001g0173 a0001c0006t0003g0025 others(128): Show |
131 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.243-772T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53950055 | |||||||
chr2:53950094 | G | C | 3 | a0001c0006t0003g0161 a0001c0006t0003g0178 a0001c0006t0003g0266 |
3 | HG00738.hp2 HG01884.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.243-811C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53950094 | |||||||
chr2:53950121 | A | G | 4 | a0005c0011t0001g0362 a0005c0011t0001g0364 a0005c0011t0002g0363 others(1): Show |
4 | HG01243.hp1 HG01891.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.243-838T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53950121 | |||||||
chr2:53950263 | G | A | 62 | a0002c0002t0002g0022 a0002c0002t0002g0023 a0002c0002t0002g0043 others(59): Show |
62 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.243-980C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53950263 | |||||||
chr2:53950275 | T | G | 1 | a0001c0009t0001g0365 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.243-992A>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53950275 | |||||||
chr2:53950285 | C | CA | 81 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0053 others(78): Show |
81 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.243-1003dupT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53950285 | |||||||
chr2:53950286 | A | C | 1 | a0003c0004t0001g0200 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.243-1003T>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53950286 | |||||||
chr2:53950311 | A | G | 1 | a0001c0005t0001g0323 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.243-1028T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53950311 | |||||||
chr2:53950398 | T | C | 50 | a0001c0001t0001g0173 a0001c0006t0003g0025 a0001c0006t0003g0026 others(47): Show |
50 | HG00099.hp2 HG00738.hp2 HG01074.hp1 others(47): Show |
intron_variant | MODIFIER | c.243-1115A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53950398 | |||||||
chr2:53950520 | G | T | 1 | a0001c0009t0013g0292 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.243-1237C>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53950520 | |||||||
chr2:53950550 | G | A | 1 | a0001c0005t0001g0351 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.243-1267C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53950550 | |||||||
chr2:53950552 | G | A | 1 | a0001c0009t0013g0292 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.243-1269C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53950552 | |||||||
chr2:53950570 | AGTGGCTC others(3481): Show |
A | 1 | a0003c0004t0001g0194 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.243-4775_243-1288d others(2): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53950570 | |||||||
chr2:53950618 | G | C | 7 | a0002c0002t0002g0044 a0002c0002t0002g0065 a0002c0002t0002g0097 others(4): Show |
7 | HG02056.hp1 NA18971.hp1 NA18972.hp2 others(4): Show |
intron_variant | MODIFIER | c.243-1335C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53950618 | |||||||
chr2:53950628 | G | C | 1 | a0002c0010t0002g0056 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.243-1345C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53950628 | |||||||
chr2:53950653 | C | T | 2 | a0003c0004t0001g0033 a0003c0004t0001g0256 |
2 | HG02027.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.243-1370G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53950653 | |||||||
chr2:53950668 | C | A | 1 | a0002c0015t0002g0359 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.243-1385G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53950668 | |||||||
chr2:53950794 | G | A | 1 | a0002c0002t0002g0357 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.243-1511C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53950794 | |||||||
chr2:53950841 | C | CA | 17 | a0001c0001t0001g0036 a0001c0001t0001g0189 a0001c0001t0001g0190 others(14): Show |
17 | HG00323.hp2 HG00733.hp1 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.243-1559dupT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53950841 | |||||||
chr2:53950929 | T | C | 3 | a0001c0006t0005g0002 a0001c0006t0005g0004 a0003c0004t0003g0218 |
3 | HG01109.hp1 HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.243-1646A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53950929 | |||||||
chr2:53950981 | T | C | 1 | a0012c0023t0003g0028 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.243-1698A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53950981 | |||||||
chr2:53950995 | T | G | 68 | a0001c0001t0001g0053 a0001c0022t0016g0111 a0002c0003t0001g0079 others(65): Show |
68 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.243-1712A>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53950995 | |||||||
chr2:53951086 | CTT | C | 5 | a0002c0002t0002g0043 a0002c0002t0002g0054 a0002c0002t0002g0081 others(2): Show |
5 | HG00280.hp2 HG00323.hp1 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.243-1805_243-1804d others(4): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53951086 | |||||||
chr2:53951149 | C | G | 7 | a0003c0004t0001g0040 a0003c0004t0001g0257 a0003c0004t0001g0274 others(4): Show |
7 | NA18959.hp2 NA18969.hp2 NA18978.hp2 others(4): Show |
intron_variant | MODIFIER | c.243-1866G>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53951149 | |||||||
chr2:53951309 | C | T | 4 | a0005c0011t0001g0362 a0005c0011t0001g0364 a0005c0011t0002g0363 others(1): Show |
4 | HG01243.hp1 HG01891.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.243-2026G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53951309 | |||||||
chr2:53951484 | G | A | 1 | a0001c0001t0001g0267 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.243-2201C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53951484 | |||||||
chr2:53951620 | T | A | 1 | a0001c0005t0001g0347 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.243-2337A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53951620 | |||||||
chr2:53951763 | C | G | 1 | a0002c0010t0002g0056 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.243-2480G>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53951763 | |||||||
chr2:53951772 | T | C | 249 | a0001c0001t0001g0053 a0001c0001t0001g0173 a0001c0005t0001g0311 others(246): Show |
249 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(246): Show |
intron_variant | MODIFIER | c.243-2489A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53951772 | |||||||
chr2:53951881 | C | T | 118 | a0001c0005t0001g0311 a0001c0005t0001g0313 a0001c0005t0001g0314 others(115): Show |
118 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.243-2598G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53951881 | |||||||
chr2:53951899 | G | A | 1 | a0001c0009t0013g0292 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.243-2616C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53951899 | |||||||
chr2:53951913 | C | T | 62 | a0002c0002t0002g0022 a0002c0002t0002g0023 a0002c0002t0002g0043 others(59): Show |
62 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.243-2630G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53951913 | |||||||
chr2:53952085 | CA | C | 49 | a0001c0001t0001g0173 a0001c0006t0003g0025 a0001c0006t0003g0026 others(46): Show |
49 | HG00099.hp2 HG00738.hp2 HG01074.hp1 others(46): Show |
intron_variant | MODIFIER | c.243-2803delT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53952085 | |||||||
chr2:53952150 | T | C | 1 | a0003c0004t0001g0254 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.243-2867A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53952150 | |||||||
chr2:53952161 | C | T | 1 | a0002c0002t0004g0118 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.243-2878G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53952161 | |||||||
chr2:53952232 | T | G | 1 | a0002c0003t0002g0127 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.243-2949A>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53952232 | |||||||
chr2:53952269 | T | C | 1 | a0001c0001t0001g0038 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.243-2986A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53952269 | |||||||
chr2:53952413 | G | A | 49 | a0001c0001t0001g0173 a0001c0006t0003g0025 a0001c0006t0003g0026 others(46): Show |
49 | HG00099.hp2 HG00738.hp2 HG01074.hp1 others(46): Show |
intron_variant | MODIFIER | c.243-3130C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53952413 | |||||||
chr2:53952491 | C | T | 3 | a0001c0001t0001g0173 a0001c0006t0003g0174 a0001c0006t0003g0217 |
3 | HG02258.hp2 HG02451.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.243-3208G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53952491 | |||||||
chr2:53952721 | G | C | 1 | a0013c0030t0002g0310 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.243-3438C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53952721 | |||||||
chr2:53952744 | T | G | 1 | a0003c0004t0003g0218 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.243-3461A>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53952744 | |||||||
chr2:53953224 | T | C | 1 | a0014c0026t0001g0013 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.243-3941A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53953224 | |||||||
chr2:53953378 | G | T | 1 | a0001c0007t0001g0179 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.243-4095C>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53953378 | |||||||
chr2:53953381 | G | C | 1 | a0016c0024t0001g0312 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.243-4098C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53953381 | |||||||
chr2:53953487 | TA | T | 238 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0035 others(235): Show |
239 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.243-4205delT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53953487 | |||||||
chr2:53953487 | TAA | T | 133 | a0001c0001t0001g0053 a0001c0001t0001g0173 a0001c0001t0001g0180 others(130): Show |
133 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.243-4206_243-4205d others(4): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53953487 | |||||||
chr2:53953504 | A | G | 3 | a0002c0003t0002g0016 a0002c0003t0002g0059 a0002c0003t0002g0072 |
3 | NA18991.hp1 NA18995.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.243-4221T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53953504 | |||||||
chr2:53953509 | A | G | 1 | a0001c0005t0001g0354 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.243-4226T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53953509 | |||||||
chr2:53953570 | A | G | 42 | a0001c0001t0001g0173 a0001c0006t0003g0025 a0001c0006t0003g0026 others(39): Show |
42 | HG00099.hp2 HG00738.hp2 HG01074.hp1 others(39): Show |
intron_variant | MODIFIER | c.243-4287T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53953570 | |||||||
chr2:53953597 | T | C | 1 | a0002c0002t0002g0153 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.243-4314A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53953597 | |||||||
chr2:53953601 | C | CT | 70 | a0001c0001t0001g0053 a0001c0007t0001g0015 a0001c0007t0001g0017 others(67): Show |
70 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.243-4319dupA | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53953601 | |||||||
chr2:53953601 | CT | C | 9 | a0001c0005t0001g0335 a0001c0006t0005g0002 a0001c0006t0005g0004 others(6): Show |
9 | HG02145.hp1 HG02559.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.243-4319delA | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53953601 | |||||||
chr2:53953713 | C | A | 1 | a0001c0005t0001g0332 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.243-4430G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53953713 | |||||||
chr2:53953844 | C | T | 1 | a0003c0004t0001g0206 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.243-4561G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53953844 | |||||||
chr2:53953845 | G | A | 5 | a0001c0006t0003g0167 a0001c0006t0003g0168 a0001c0006t0003g0170 others(2): Show |
5 | HG02630.hp2 HG02896.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.243-4562C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53953845 | |||||||
chr2:53953881 | C | T | 1 | a0002c0002t0002g0142 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.243-4598G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53953881 | |||||||
chr2:53953955 | A | C | 4 | a0003c0004t0001g0262 a0003c0004t0001g0263 a0003c0004t0001g0264 others(1): Show |
4 | NA18983.hp2 NA19004.hp1 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.243-4672T>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53953955 | |||||||
chr2:53953998 | G | A | 3 | a0002c0002t0002g0096 a0002c0002t0004g0095 a0002c0002t0004g0118 |
3 | HG00621.hp2 HG02523.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.243-4715C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53953998 | |||||||
chr2:53954096 | G | A | 1 | a0001c0001t0001g0267 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.243-4813C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53954096 | |||||||
chr2:53954122 | G | T | 2 | a0001c0006t0005g0002 a0001c0006t0005g0004 |
2 | HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.243-4839C>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53954122 | |||||||
chr2:53954126 | G | A | 4 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0270 others(1): Show |
4 | HG01175.hp2 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.243-4843C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53954126 | |||||||
chr2:53954185 | G | A | 2 | a0003c0004t0001g0033 a0003c0004t0001g0256 |
2 | HG02027.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.243-4902C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53954185 | |||||||
chr2:53954221 | G | A | 4 | a0003c0004t0001g0262 a0003c0004t0001g0263 a0003c0004t0001g0264 others(1): Show |
4 | NA18983.hp2 NA19004.hp1 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.243-4938C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53954221 | |||||||
chr2:53954247 | G | C | 1 | a0001c0001t0001g0038 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.243-4964C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53954247 | |||||||
chr2:53954326 | T | C | 126 | a0001c0005t0001g0311 a0001c0005t0001g0313 a0001c0005t0001g0314 others(123): Show |
126 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.243-5043A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53954326 | |||||||
chr2:53954366 | G | A | 1 | a0001c0001t0012g0041 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.243-5083C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53954366 | |||||||
chr2:53954392 | C | T | 68 | a0001c0001t0001g0053 a0001c0022t0016g0111 a0002c0003t0001g0079 others(65): Show |
68 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.243-5109G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53954392 | |||||||
chr2:53954480 | T | C | 1 | a0001c0005t0001g0314 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.243-5197A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53954480 | |||||||
chr2:53954733 | T | A | 1 | a0001c0001t0001g0237 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.243-5450A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53954733 | |||||||
chr2:53954809 | C | G | 1 | a0001c0005t0001g0341 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.243-5526G>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53954809 | |||||||
chr2:53954900 | C | T | 1 | a0001c0001t0001g0001 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.243-5617G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53954900 | |||||||
chr2:53954928 | C | G | 1 | a0013c0030t0002g0310 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.243-5645G>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53954928 | |||||||
chr2:53954972 | G | A | 5 | a0001c0001t0001g0181 a0001c0001t0001g0191 a0001c0001t0001g0239 others(2): Show |
5 | HG01255.hp2 HG02976.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.243-5689C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53954972 | |||||||
chr2:53955041 | C | A | 2 | a0001c0001t0001g0204 a0001c0001t0001g0238 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.243-5758G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53955041 | |||||||
chr2:53955142 | G | C | 1 | a0001c0005t0001g0347 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.243-5859C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53955142 | |||||||
chr2:53955242 | A | G | 1 | a0002c0029t0002g0307 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.243-5959T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53955242 | |||||||
chr2:53955342 | C | T | 4 | a0002c0003t0002g0070 a0002c0003t0002g0071 a0002c0003t0002g0080 others(1): Show |
4 | NA18970.hp1 NA18984.hp1 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.243-6059G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53955342 | |||||||
chr2:53955361 | A | C | 1 | a0001c0005t0001g0342 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.243-6078T>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53955361 | |||||||
chr2:53955410 | C | T | 1 | a0001c0001t0012g0041 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.243-6127G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53955410 | |||||||
chr2:53955411 | G | A | 2 | a0002c0003t0002g0019 a0013c0030t0002g0310 |
2 | HG02717.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.243-6128C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53955411 | |||||||
chr2:53955479 | C | T | 2 | a0001c0006t0005g0002 a0001c0006t0005g0004 |
2 | HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.243-6196G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53955479 | |||||||
chr2:53955578 | C | G | 64 | a0001c0001t0001g0053 a0001c0007t0001g0015 a0001c0007t0001g0017 others(61): Show |
64 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.243-6295G>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53955578 | |||||||
chr2:53955610 | A | C | 1 | a0002c0002t0002g0093 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.243-6327T>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53955610 | |||||||
chr2:53955761 | G | C | 253 | a0001c0001t0001g0053 a0001c0001t0001g0173 a0001c0005t0001g0311 others(250): Show |
253 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.243-6478C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53955761 | |||||||
chr2:53955836 | T | A | 2 | a0001c0007t0001g0015 a0001c0007t0001g0017 |
2 | HG01081.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.243-6553A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53955836 | |||||||
chr2:53955890 | C | G | 3 | a0001c0006t0005g0002 a0001c0006t0005g0004 a0002c0003t0010g0006 |
3 | HG02145.hp1 HG02809.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.243-6607G>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53955890 | |||||||
chr2:53955922 | A | C | 1 | a0001c0006t0003g0155 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.243-6639T>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53955922 | |||||||
chr2:53955927 | A | C | 1 | a0002c0010t0002g0051 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.243-6644T>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53955927 | |||||||
chr2:53955929 | C | A | 1 | a0001c0001t0001g0282 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.243-6646G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53955929 | |||||||
chr2:53955987 | A | T | 1 | a0002c0002t0002g0358 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.243-6704T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53955987 | |||||||
chr2:53955990 | T | G | 1 | a0003c0004t0001g0039 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.243-6707A>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53955990 | |||||||
chr2:53956083 | G | A | 1 | a0002c0003t0002g0060 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.243-6800C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53956083 | |||||||
chr2:53956094 | G | C | 1 | a0011c0016t0001g0339 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.243-6811C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53956094 | |||||||
chr2:53956358 | G | A | 5 | a0002c0002t0002g0047 a0002c0002t0002g0068 a0002c0002t0002g0091 others(2): Show |
5 | HG02040.hp2 NA18965.hp2 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.243-7075C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53956358 | |||||||
chr2:53956390 | C | A | 1 | a0002c0002t0002g0093 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.243-7107G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53956390 | |||||||
chr2:53956445 | G | A | 5 | a0001c0006t0003g0155 a0001c0006t0003g0156 a0001c0006t0003g0157 others(2): Show |
5 | HG01167.hp2 HG02886.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.243-7162C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53956445 | |||||||
chr2:53956617 | A | T | 1 | a0001c0005t0001g0341 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.243-7334T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53956617 | |||||||
chr2:53956671 | T | G | 11 | a0003c0004t0001g0183 a0003c0004t0001g0195 a0003c0004t0001g0258 others(8): Show |
11 | HG00558.hp2 HG00735.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.243-7388A>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53956671 | |||||||
chr2:53956860 | T | C | 1 | a0002c0002t0002g0153 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.243-7577A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53956860 | |||||||
chr2:53957116 | T | A | 1 | a0001c0001t0001g0275 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.243-7833A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53957116 | |||||||
chr2:53957162 | G | A | 1 | a0005c0011t0001g0364 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.243-7879C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53957162 | |||||||
chr2:53957392 | A | C | 1 | a0001c0005t0001g0348 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.243-8109T>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53957392 | |||||||
chr2:53957408 | T | C | 72 | a0001c0001t0001g0053 a0001c0007t0001g0015 a0001c0007t0001g0017 others(69): Show |
72 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.243-8125A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53957408 | |||||||
chr2:53957415 | G | A | 1 | a0002c0002t0002g0355 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.243-8132C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53957415 | |||||||
chr2:53957436 | T | C | 1 | a0002c0010t0002g0018 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.243-8153A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53957436 | |||||||
chr2:53957665 | A | G | 3 | a0001c0001t0001g0181 a0001c0001t0001g0239 a0001c0001t0001g0240 |
3 | HG01255.hp2 HG03486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.243-8382T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53957665 | |||||||
chr2:53957845 | A | G | 1 | a0016c0024t0001g0312 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.243-8562T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53957845 | |||||||
chr2:53957849 | T | C | 1 | a0001c0001t0012g0041 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.243-8566A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53957849 | |||||||
chr2:53957891 | C | A | 2 | a0001c0006t0003g0172 a0001c0006t0003g0175 |
2 | HG02257.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.243-8608G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53957891 | |||||||
chr2:53957893 | T | A | 2 | a0001c0006t0003g0172 a0001c0006t0003g0175 |
2 | HG02257.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.243-8610A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53957893 | |||||||
chr2:53958004 | A | G | 252 | a0001c0001t0001g0053 a0001c0001t0001g0173 a0001c0005t0001g0311 others(249): Show |
252 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(249): Show |
intron_variant | MODIFIER | c.243-8721T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53958004 | |||||||
chr2:53958099 | T | A | 2 | a0002c0003t0002g0134 a0002c0003t0002g0135 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.243-8816A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53958099 | |||||||
chr2:53958155 | C | T | 1 | a0003c0004t0001g0291 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.243-8872G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53958155 | |||||||
chr2:53958183 | C | CA | 35 | a0001c0001t0001g0038 a0001c0001t0001g0053 a0001c0001t0001g0181 others(32): Show |
35 | HG00438.hp1 HG00597.hp2 HG01192.hp1 others(32): Show |
intron_variant | MODIFIER | c.243-8901dupT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53958183 | |||||||
chr2:53958183 | CA | C | 12 | a0001c0001t0001g0214 a0001c0001t0001g0223 a0001c0001t0007g0222 others(9): Show |
12 | HG01069.hp2 HG01070.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.243-8901delT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53958183 | |||||||
chr2:53958183 | CAAAAAAA | C | 8 | a0002c0003t0002g0024 a0002c0003t0002g0136 a0002c0003t0002g0144 others(5): Show |
8 | HG00733.hp2 HG01123.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.243-8907_243-8901d others(9): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53958183 | |||||||
chr2:53958328 | G | T | 1 | a0001c0001t0001g0010 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.243-9045C>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53958328 | |||||||
chr2:53958356 | AAAAAAAA others(1): Show |
A | 65 | a0001c0001t0001g0053 a0001c0022t0016g0111 a0002c0003t0001g0079 others(62): Show |
65 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.243-9081_243-9074d others(10): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53958356 | |||||||
chr2:53958467 | A | C | 2 | a0002c0003t0002g0134 a0002c0003t0002g0135 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.243-9184T>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53958467 | |||||||
chr2:53958510 | C | T | 48 | a0001c0001t0001g0173 a0001c0006t0003g0025 a0001c0006t0003g0026 others(45): Show |
48 | HG00099.hp2 HG00738.hp2 HG01074.hp1 others(45): Show |
intron_variant | MODIFIER | c.243-9227G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53958510 | |||||||
chr2:53958604 | A | G | 1 | a0001c0001t0001g0267 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.243-9321T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53958604 | |||||||
chr2:53958607 | T | C | 5 | a0001c0006t0005g0002 a0001c0006t0005g0004 a0002c0003t0010g0006 others(2): Show |
5 | HG01109.hp1 HG02145.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.243-9324A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53958607 | |||||||
chr2:53958726 | G | C | 1 | a0003c0004t0001g0257 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.243-9443C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53958726 | |||||||
chr2:53958818 | T | TA | 12 | a0001c0005t0001g0329 a0003c0004t0001g0183 a0003c0004t0001g0195 others(9): Show |
12 | HG00558.hp2 HG00735.hp2 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.243-9536dupT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53958818 | |||||||
chr2:53958818 | TA | T | 9 | a0001c0005t0001g0319 a0001c0006t0005g0002 a0001c0006t0005g0004 others(6): Show |
9 | HG01109.hp1 HG01256.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.243-9536delT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53958818 | |||||||
chr2:53958834 | G | A | 1 | a0002c0003t0002g0019 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.243-9551C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53958834 | |||||||
chr2:53958899 | C | T | 2 | a0003c0004t0001g0192 a0003c0004t0001g0245 |
2 | HG02622.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.243-9616G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53958899 | |||||||
chr2:53958916 | A | G | 253 | a0001c0001t0001g0053 a0001c0001t0001g0173 a0001c0005t0001g0311 others(250): Show |
253 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.243-9633T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53958916 | |||||||
chr2:53959053 | C | T | 1 | a0002c0003t0002g0049 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.243-9770G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53959053 | |||||||
chr2:53959107 | A | G | 3 | a0001c0005t0001g0316 a0001c0005t0001g0318 a0001c0005t0001g0353 |
3 | HG01515.hp2 HG01517.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.243-9824T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53959107 | |||||||
chr2:53959122 | G | C | 1 | a0001c0009t0013g0292 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.243-9839C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53959122 | |||||||
chr2:53959128 | G | C | 1 | a0001c0009t0013g0292 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.243-9845C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53959128 | |||||||
chr2:53959268 | G | C | 1 | a0016c0024t0001g0312 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.243-9985C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53959268 | |||||||
chr2:53959343 | T | A | 66 | a0001c0001t0001g0053 a0001c0022t0016g0111 a0002c0003t0001g0079 others(63): Show |
66 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.243-10060A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53959343 | |||||||
chr2:53959399 | C | T | 66 | a0001c0001t0001g0053 a0001c0022t0016g0111 a0002c0003t0001g0079 others(63): Show |
66 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.243-10116G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53959399 | |||||||
chr2:53959470 | C | T | 1 | a0003c0004t0001g0183 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.243-10187G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53959470 | |||||||
chr2:53959532 | A | G | 1 | a0001c0007t0001g0361 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.243-10249T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53959532 | |||||||
chr2:53959745 | A | C | 1 | a0013c0030t0002g0310 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.243-10462T>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53959745 | |||||||
chr2:53959863 | G | C | 4 | a0001c0001t0001g0181 a0001c0001t0001g0239 a0001c0001t0001g0240 others(1): Show |
4 | HG01255.hp2 HG03225.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.243-10580C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53959863 | |||||||
chr2:53959869 | C | A | 1 | a0002c0002t0002g0094 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.243-10586G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53959869 | |||||||
chr2:53959876 | C | T | 1 | a0003c0004t0001g0269 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.243-10593G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53959876 | |||||||
chr2:53959891 | G | A | 2 | a0001c0005t0001g0352 a0002c0003t0004g0340 |
2 | NA19055.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.243-10608C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53959891 | |||||||
chr2:53959922 | C | T | 1 | a0001c0001t0001g0035 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.242+10621G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53959922 | |||||||
chr2:53960169 | G | T | 1 | a0001c0001t0001g0267 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.242+10374C>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53960169 | |||||||
chr2:53960206 | C | T | 1 | a0002c0002t0002g0115 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.242+10337G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53960206 | |||||||
chr2:53960215 | C | A | 1 | a0001c0009t0013g0292 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.242+10328G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53960215 | |||||||
chr2:53960216 | A | T | 1 | a0001c0009t0013g0292 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.242+10327T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53960216 | |||||||
chr2:53960221 | G | A | 5 | a0001c0009t0001g0360 a0001c0009t0001g0366 a0001c0009t0001g0367 others(2): Show |
5 | HG02717.hp1 HG02818.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.242+10322C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53960221 | |||||||
chr2:53960269 | G | T | 1 | a0013c0030t0002g0310 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.242+10274C>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53960269 | |||||||
chr2:53960381 | A | G | 1 | a0002c0002t0002g0115 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.242+10162T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53960381 | |||||||
chr2:53960398 | C | CA | 8 | a0001c0001t0001g0241 a0001c0005t0001g0344 a0001c0006t0003g0172 others(5): Show |
8 | HG00735.hp2 HG02145.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.242+10144dupT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53960398 | |||||||
chr2:53960480 | A | G | 50 | a0001c0001t0001g0173 a0001c0006t0003g0025 a0001c0006t0003g0026 others(47): Show |
50 | HG00099.hp2 HG00738.hp2 HG01074.hp1 others(47): Show |
intron_variant | MODIFIER | c.242+10063T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53960480 | |||||||
chr2:53960507 | C | T | 4 | a0001c0001t0001g0180 a0001c0001t0001g0214 a0001c0001t0001g0215 others(1): Show |
4 | HG02630.hp1 HG03130.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.242+10036G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53960507 | |||||||
chr2:53960523 | T | C | 1 | a0001c0007t0001g0361 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.242+10020A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53960523 | |||||||
chr2:53960585 | C | G | 3 | a0002c0010t0002g0018 a0002c0010t0002g0051 a0002c0010t0002g0056 |
3 | HG02572.hp1 HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.242+9958G>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53960585 | |||||||
chr2:53960709 | C | T | 377 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0035 others(374): Show |
378 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(375): Show |
intron_variant | MODIFIER | c.242+9834G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53960709 | |||||||
chr2:53960731 | T | G | 58 | a0002c0029t0002g0307 a0003c0004t0001g0032 a0003c0004t0001g0033 others(55): Show |
58 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.242+9812A>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53960731 | |||||||
chr2:53960750 | G | A | 1 | a0001c0009t0013g0292 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.242+9793C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53960750 | |||||||
chr2:53960826 | G | A | 1 | a0003c0004t0001g0291 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.242+9717C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53960826 | |||||||
chr2:53960889 | C | T | 7 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0186 others(4): Show |
7 | HG00738.hp1 HG01123.hp1 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.242+9654G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53960889 | |||||||
chr2:53960906 | G | C | 2 | a0002c0002t0002g0096 a0002c0002t0004g0095 |
2 | HG02523.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.242+9637C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53960906 | |||||||
chr2:53961159 | A | G | 5 | a0001c0007t0006g0012 a0001c0007t0006g0014 a0001c0007t0006g0196 others(2): Show |
5 | HG02559.hp2 HG02965.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.242+9384T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53961159 | |||||||
chr2:53961257 | T | A | 2 | a0001c0007t0001g0015 a0001c0007t0001g0017 |
2 | HG01081.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.242+9286A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53961257 | |||||||
chr2:53961434 | C | T | 1 | a0001c0001t0001g0211 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.242+9109G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53961434 | |||||||
chr2:53961514 | T | C | 1 | a0006c0012t0002g0062 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.242+9029A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53961514 | |||||||
chr2:53961583 | T | C | 1 | a0001c0001t0001g0001 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.242+8960A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53961583 | |||||||
chr2:53961672 | T | C | 5 | a0001c0007t0006g0012 a0001c0007t0006g0014 a0001c0007t0006g0196 others(2): Show |
5 | HG02559.hp2 HG02965.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.242+8871A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53961672 | |||||||
chr2:53961673 | C | A | 5 | a0001c0007t0006g0012 a0001c0007t0006g0014 a0001c0007t0006g0196 others(2): Show |
5 | HG02559.hp2 HG02965.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.242+8870G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53961673 | |||||||
chr2:53961932 | C | T | 60 | a0001c0001t0001g0053 a0001c0022t0016g0111 a0002c0003t0001g0079 others(57): Show |
60 | HG00408.hp2 HG00558.hp1 HG00733.hp2 others(57): Show |
intron_variant | MODIFIER | c.242+8611G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53961932 | |||||||
chr2:53962059 | C | T | 1 | a0003c0004t0001g0298 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.242+8484G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53962059 | |||||||
chr2:53962121 | G | T | 2 | a0001c0006t0005g0002 a0001c0006t0005g0004 |
2 | HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.242+8422C>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53962121 | |||||||
chr2:53962140 | T | C | 13 | a0001c0001t0001g0273 a0001c0001t0012g0041 a0002c0002t0002g0044 others(10): Show |
13 | HG00323.hp2 HG00544.hp1 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.242+8403A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53962140 | |||||||
chr2:53962147 | C | G | 2 | a0002c0003t0002g0144 a0016c0024t0001g0312 |
2 | HG03579.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.242+8396G>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53962147 | |||||||
chr2:53962150 | C | T | 2 | a0002c0003t0002g0144 a0016c0024t0001g0312 |
2 | HG03579.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.242+8393G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53962150 | |||||||
chr2:53962157 | G | T | 1 | a0002c0003t0002g0069 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.242+8386C>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53962157 | |||||||
chr2:53962240 | T | C | 4 | a0001c0005t0001g0341 a0002c0002t0002g0100 a0002c0002t0002g0126 others(1): Show |
4 | HG02572.hp2 NA19002.hp2 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.242+8303A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53962240 | |||||||
chr2:53962375 | G | T | 2 | a0001c0001t0001g0267 a0001c0006t0003g0266 |
2 | HG01884.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.242+8168C>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53962375 | |||||||
chr2:53962589 | C | A | 1 | a0001c0005t0001g0182 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.242+7954G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53962589 | |||||||
chr2:53962650 | T | C | 1 | a0001c0007t0001g0361 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.242+7893A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53962650 | |||||||
chr2:53962700 | T | C | 1 | a0001c0005t0001g0372 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.242+7843A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53962700 | |||||||
chr2:53962826 | T | A | 1 | a0002c0003t0002g0127 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.242+7717A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53962826 | |||||||
chr2:53962876 | T | C | 1 | a0002c0003t0002g0148 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.242+7667A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53962876 | |||||||
chr2:53962941 | T | C | 1 | a0002c0003t0002g0011 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.242+7602A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53962941 | |||||||
chr2:53962966 | C | T | 1 | a0001c0007t0006g0014 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.242+7577G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53962966 | |||||||
chr2:53962967 | G | C | 1 | a0001c0007t0001g0361 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.242+7576C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53962967 | |||||||
chr2:53963009 | C | CA | 7 | a0001c0001t0001g0205 a0001c0001t0001g0267 a0001c0005t0001g0342 others(4): Show |
7 | HG00597.hp2 HG01884.hp1 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.242+7533dupT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53963009 | |||||||
chr2:53963009 | CA | C | 12 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0210 others(9): Show |
12 | HG02145.hp2 HG02258.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.242+7533delT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53963009 | |||||||
chr2:53963025 | A | G | 3 | a0001c0006t0005g0002 a0001c0006t0005g0004 a0002c0003t0010g0006 |
3 | HG02145.hp1 HG02809.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.242+7518T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53963025 | |||||||
chr2:53963102 | G | A | 1 | a0002c0003t0002g0127 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.242+7441C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53963102 | |||||||
chr2:53963190 | G | A | 1 | a0014c0026t0001g0013 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.242+7353C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53963190 | |||||||
chr2:53963237 | G | A | 3 | a0001c0006t0005g0002 a0001c0006t0005g0004 a0002c0003t0010g0006 |
3 | HG02145.hp1 HG02809.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.242+7306C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53963237 | |||||||
chr2:53963284 | G | A | 1 | a0001c0006t0003g0172 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.242+7259C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53963284 | |||||||
chr2:53963396 | A | C | 3 | a0001c0005t0001g0316 a0001c0005t0001g0318 a0001c0005t0001g0353 |
3 | HG01515.hp2 HG01517.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.242+7147T>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53963396 | |||||||
chr2:53963449 | T | A | 3 | a0001c0006t0005g0002 a0001c0006t0005g0004 a0002c0003t0010g0006 |
3 | HG02145.hp1 HG02809.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.242+7094A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53963449 | |||||||
chr2:53963485 | A | G | 1 | a0001c0006t0003g0172 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.242+7058T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53963485 | |||||||
chr2:53963613 | A | T | 5 | a0003c0004t0001g0032 a0003c0004t0001g0034 a0003c0004t0001g0206 others(2): Show |
5 | NA18945.hp1 NA18955.hp1 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.242+6930T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53963613 | |||||||
chr2:53963663 | A | G | 1 | a0002c0032t0004g0374 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.242+6880T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53963663 | |||||||
chr2:53963832 | C | T | 1 | a0001c0006t0003g0167 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.242+6711G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53963832 | |||||||
chr2:53963839 | T | A | 1 | a0010c0027t0003g0162 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.242+6704A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53963839 | |||||||
chr2:53964110 | T | C | 1 | a0001c0006t0015g0169 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.242+6433A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53964110 | |||||||
chr2:53964325 | G | A | 3 | a0002c0010t0002g0018 a0002c0010t0002g0051 a0002c0010t0002g0056 |
3 | HG02572.hp1 HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.242+6218C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53964325 | |||||||
chr2:53964337 | T | G | 1 | a0001c0009t0013g0292 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.242+6206A>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53964337 | |||||||
chr2:53964370 | T | C | 1 | a0001c0001t0001g0184 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.242+6173A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53964370 | |||||||
chr2:53964657 | C | T | 9 | a0001c0005t0001g0317 a0001c0005t0001g0325 a0001c0005t0001g0326 others(6): Show |
9 | HG00597.hp1 HG02129.hp1 NA18943.hp1 others(6): Show |
intron_variant | MODIFIER | c.242+5886G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53964657 | |||||||
chr2:53964858 | G | C | 1 | a0012c0023t0003g0028 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.242+5685C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53964858 | |||||||
chr2:53964862 | A | G | 1 | a0010c0027t0003g0162 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.242+5681T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53964862 | |||||||
chr2:53965020 | G | A | 245 | a0001c0001t0001g0053 a0001c0001t0001g0173 a0001c0001t0001g0293 others(242): Show |
245 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.242+5523C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53965020 | |||||||
chr2:53965068 | A | C | 5 | a0001c0006t0005g0002 a0001c0006t0005g0003 a0001c0006t0005g0004 others(2): Show |
5 | HG02109.hp1 HG02145.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.242+5475T>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53965068 | |||||||
chr2:53965095 | A | G | 3 | a0001c0006t0003g0163 a0001c0006t0003g0165 a0001c0006t0003g0166 |
3 | NA18951.hp2 NA18973.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.242+5448T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53965095 | |||||||
chr2:53965102 | G | GAC | 3 | a0001c0007t0006g0012 a0001c0007t0006g0014 a0014c0026t0001g0013 |
3 | HG02559.hp2 HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.242+5439_242+5440d others(4): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53965102 | |||||||
chr2:53965175 | T | G | 1 | a0002c0029t0002g0307 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.242+5368A>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53965175 | |||||||
chr2:53965246 | A | AT | 19 | a0001c0001t0001g0173 a0001c0001t0001g0184 a0001c0001t0001g0204 others(16): Show |
19 | HG00597.hp1 HG00597.hp2 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.242+5296dupA | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53965246 | |||||||
chr2:53965246 | AT | A | 130 | a0001c0001t0001g0053 a0001c0006t0003g0371 a0001c0006t0005g0002 others(127): Show |
130 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.242+5296delA | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53965246 | |||||||
chr2:53965328 | A | G | 1 | a0002c0029t0002g0307 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.242+5215T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53965328 | |||||||
chr2:53965525 | G | A | 4 | a0002c0002t0002g0356 a0002c0002t0002g0357 a0002c0002t0002g0358 others(1): Show |
4 | HG01255.hp1 HG02615.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.242+5018C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53965525 | |||||||
chr2:53965554 | TGAG | T | 125 | a0001c0001t0001g0053 a0001c0022t0016g0111 a0002c0002t0002g0022 others(122): Show |
125 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.242+4986_242+4988d others(5): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53965554 | |||||||
chr2:53965622 | C | T | 1 | a0003c0004t0001g0271 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.242+4921G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53965622 | |||||||
chr2:53965659 | T | C | 2 | a0003c0004t0001g0032 a0003c0004t0001g0268 |
2 | NA18945.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.242+4884A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53965659 | |||||||
chr2:53965663 | T | A | 1 | a0010c0027t0003g0162 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.242+4880A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53965663 | |||||||
chr2:53965670 | G | GT | 224 | a0001c0001t0001g0053 a0001c0001t0001g0173 a0001c0001t0001g0293 others(221): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(221): Show |
intron_variant | MODIFIER | c.242+4872dupA | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53965670 | |||||||
chr2:53965670 | G | GTT | 9 | a0001c0006t0003g0167 a0001c0006t0003g0168 a0001c0006t0003g0170 others(6): Show |
9 | HG00438.hp1 HG02630.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.242+4871_242+4872d others(4): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53965670 | |||||||
chr2:53965690 | G | A | 1 | a0003c0004t0001g0269 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.242+4853C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53965690 | |||||||
chr2:53965792 | C | T | 4 | a0001c0006t0005g0002 a0001c0006t0005g0003 a0001c0006t0005g0004 others(1): Show |
4 | HG02109.hp1 HG02145.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.242+4751G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53965792 | |||||||
chr2:53965810 | C | A | 1 | a0001c0007t0001g0015 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.242+4733G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53965810 | |||||||
chr2:53965962 | A | G | 245 | a0001c0001t0001g0053 a0001c0001t0001g0173 a0001c0001t0001g0293 others(242): Show |
245 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.242+4581T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53965962 | |||||||
chr2:53966056 | T | C | 248 | a0001c0001t0001g0053 a0001c0001t0001g0173 a0001c0001t0001g0198 others(245): Show |
248 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.242+4487A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53966056 | |||||||
chr2:53966088 | C | A | 1 | a0002c0003t0002g0128 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.242+4455G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53966088 | |||||||
chr2:53966237 | T | C | 4 | a0001c0006t0005g0002 a0001c0006t0005g0003 a0001c0006t0005g0004 others(1): Show |
4 | HG02109.hp1 HG02145.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.242+4306A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53966237 | |||||||
chr2:53966430 | G | A | 5 | a0002c0002t0002g0045 a0002c0002t0002g0102 a0002c0002t0002g0103 others(2): Show |
5 | NA18941.hp1 NA18961.hp1 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.242+4113C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53966430 | |||||||
chr2:53966443 | T | C | 1 | a0016c0024t0001g0312 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.242+4100A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53966443 | |||||||
chr2:53966528 | G | A | 5 | a0001c0006t0003g0167 a0001c0006t0003g0168 a0001c0006t0003g0170 others(2): Show |
5 | HG02630.hp2 HG02896.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.242+4015C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53966528 | |||||||
chr2:53966554 | C | T | 3 | a0003c0004t0001g0200 a0003c0004t0001g0201 a0003c0004t0001g0202 |
3 | NA18948.hp2 NA18952.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.242+3989G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53966554 | |||||||
chr2:53966659 | T | A | 1 | a0001c0005t0001g0343 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.242+3884A>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53966659 | |||||||
chr2:53966659 | T | C | 1 | a0002c0002t0002g0131 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.242+3884A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53966659 | |||||||
chr2:53966703 | G | T | 1 | a0001c0005t0001g0344 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.242+3840C>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53966703 | |||||||
chr2:53966716 | T | C | 7 | a0001c0006t0003g0371 a0001c0009t0001g0360 a0001c0009t0001g0366 others(4): Show |
7 | HG01074.hp1 HG02647.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.242+3827A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53966716 | |||||||
chr2:53966751 | G | A | 128 | a0001c0001t0001g0053 a0001c0005t0001g0324 a0001c0007t0001g0015 others(125): Show |
128 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.242+3792C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53966751 | |||||||
chr2:53966830 | G | C | 1 | a0001c0007t0001g0015 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.242+3713C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53966830 | |||||||
chr2:53966920 | G | A | 1 | a0001c0006t0003g0159 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.242+3623C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53966920 | |||||||
chr2:53966934 | G | A | 239 | a0001c0001t0001g0053 a0001c0001t0001g0173 a0001c0005t0001g0311 others(236): Show |
239 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.242+3609C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53966934 | |||||||
chr2:53966950 | G | A | 1 | a0001c0001t0001g0010 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.242+3593C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53966950 | |||||||
chr2:53967044 | G | A | 1 | a0003c0004t0001g0271 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.242+3499C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53967044 | |||||||
chr2:53967199 | C | T | 1 | a0002c0003t0002g0055 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.242+3344G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53967199 | |||||||
chr2:53967241 | C | T | 1 | a0001c0007t0001g0361 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.242+3302G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53967241 | |||||||
chr2:53967280 | T | C | 2 | a0001c0001t0001g0272 a0001c0001t0001g0273 |
2 | HG00323.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.242+3263A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53967280 | |||||||
chr2:53967294 | C | T | 123 | a0001c0001t0001g0053 a0001c0022t0016g0111 a0002c0002t0002g0022 others(120): Show |
123 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.242+3249G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53967294 | |||||||
chr2:53967314 | C | T | 1 | a0002c0003t0002g0066 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.242+3229G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53967314 | |||||||
chr2:53967449 | C | T | 4 | a0001c0006t0005g0002 a0001c0006t0005g0003 a0001c0006t0005g0004 others(1): Show |
4 | HG02109.hp1 HG02145.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.242+3094G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53967449 | |||||||
chr2:53967583 | G | A | 3 | a0001c0006t0003g0031 a0001c0006t0003g0176 a0001c0006t0003g0177 |
3 | HG02615.hp1 HG02970.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.242+2960C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53967583 | |||||||
chr2:53967611 | A | G | 240 | a0001c0001t0001g0053 a0001c0001t0001g0173 a0001c0005t0001g0311 others(237): Show |
240 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.242+2932T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53967611 | |||||||
chr2:53967649 | C | CA | 35 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0038 others(32): Show |
35 | HG00099.hp1 HG00438.hp2 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.242+2893dupT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53967649 | |||||||
chr2:53967649 | C | CAA | 12 | a0001c0001t0012g0041 a0002c0002t0002g0357 a0002c0003t0002g0297 others(9): Show |
12 | HG02132.hp1 HG02572.hp2 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.242+2892_242+2893d others(4): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53967649 | |||||||
chr2:53967649 | C | CAAAA | 7 | a0001c0001t0001g0053 a0001c0009t0001g0365 a0002c0002t0002g0054 others(4): Show |
7 | HG01255.hp1 HG02155.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.242+2890_242+2893d others(6): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53967649 | |||||||
chr2:53967649 | C | CAAAAA | 17 | a0001c0006t0003g0025 a0001c0006t0003g0026 a0001c0006t0003g0027 others(14): Show |
17 | HG00099.hp2 HG01099.hp2 HG01516.hp2 others(14): Show |
intron_variant | MODIFIER | c.242+2889_242+2893d others(7): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53967649 | |||||||
chr2:53967649 | C | CAAAAAA | 61 | a0001c0005t0001g0315 a0001c0006t0003g0029 a0001c0006t0003g0030 others(58): Show |
61 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.242+2888_242+2893d others(8): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53967649 | |||||||
chr2:53967649 | C | CAAAAAAA | 54 | a0001c0005t0001g0316 a0001c0005t0001g0317 a0001c0005t0001g0318 others(51): Show |
54 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.242+2887_242+2893d others(9): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53967649 | |||||||
chr2:53967649 | C | CAAAAAAA others(1): Show |
40 | a0001c0005t0001g0326 a0001c0005t0001g0327 a0001c0005t0001g0328 others(37): Show |
40 | HG00438.hp1 HG00597.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.242+2886_242+2893d others(10): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53967649 | |||||||
chr2:53967649 | C | CAAAAAAA others(2): Show |
23 | a0001c0001t0001g0173 a0001c0005t0001g0311 a0001c0005t0001g0344 others(20): Show |
23 | HG00423.hp1 HG00609.hp1 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.242+2885_242+2893d others(11): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53967649 | |||||||
chr2:53967649 | C | CAAAAAAA others(3): Show |
5 | a0001c0005t0001g0353 a0001c0006t0003g0177 a0002c0002t0002g0151 others(2): Show |
5 | HG01123.hp2 HG01256.hp2 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.242+2884_242+2893d others(12): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53967649 | |||||||
chr2:53967649 | C | CAAAAAAA others(4): Show |
2 | a0001c0006t0003g0031 a0001c0006t0003g0178 |
2 | HG02559.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.242+2883_242+2893d others(13): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53967649 | |||||||
chr2:53967649 | C | CAAAAAAA others(5): Show |
1 | a0001c0005t0001g0354 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.242+2882_242+2893d others(14): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53967649 | |||||||
chr2:53967649 | C | CAAAAAAA others(30): Show |
1 | a0001c0005t0001g0325 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.242+2893_242+2894i others(39): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53967649 | |||||||
chr2:53967649 | CA | C | 12 | a0001c0001t0001g0180 a0001c0001t0001g0189 a0001c0001t0001g0190 others(9): Show |
12 | HG01361.hp1 HG01516.hp1 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.242+2893delT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53967649 | |||||||
chr2:53967649 | CAAAAAAA others(1): Show |
C | 6 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0186 others(3): Show |
6 | HG00738.hp1 HG01123.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.242+2886_242+2893d others(10): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53967649 | |||||||
chr2:53967649 | CAAAAAAA others(5): Show |
C | 1 | a0001c0009t0001g0360 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.242+2882_242+2893d others(14): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53967649 | |||||||
chr2:53967649 | CAAAAAAA others(6): Show |
C | 5 | a0001c0006t0003g0155 a0001c0006t0003g0156 a0001c0006t0003g0157 others(2): Show |
5 | HG01167.hp2 HG02886.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.242+2881_242+2893d others(15): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53967649 | |||||||
chr2:53967649 | CAAAAAAA others(8): Show |
C | 1 | a0014c0026t0001g0013 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.242+2879_242+2893d others(17): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53967649 | |||||||
chr2:53967649 | CAAAAAAA others(10): Show |
C | 1 | a0003c0004t0001g0183 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.242+2877_242+2893d others(19): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53967649 | |||||||
chr2:53967649 | CAAAAAAA others(12): Show |
C | 1 | a0001c0005t0001g0182 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.242+2875_242+2893d others(21): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53967649 | |||||||
chr2:53967679 | A | G | 2 | a0001c0006t0005g0002 a0001c0006t0005g0003 |
2 | HG02976.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.242+2864T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53967679 | |||||||
chr2:53967797 | C | G | 240 | a0001c0001t0001g0053 a0001c0001t0001g0173 a0001c0005t0001g0311 others(237): Show |
240 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.242+2746G>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53967797 | |||||||
chr2:53967848 | T | C | 1 | a0002c0002t0002g0355 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.242+2695A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53967848 | |||||||
chr2:53967908 | A | G | 4 | a0002c0002t0002g0356 a0002c0002t0002g0357 a0002c0002t0002g0358 others(1): Show |
4 | HG01255.hp1 HG02615.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.242+2635T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53967908 | |||||||
chr2:53967934 | T | C | 1 | a0001c0005t0001g0373 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.242+2609A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53967934 | |||||||
chr2:53968139 | G | C | 1 | a0002c0003t0002g0152 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.242+2404C>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53968139 | |||||||
chr2:53968147 | C | T | 55 | a0001c0005t0001g0311 a0001c0005t0001g0313 a0001c0005t0001g0314 others(52): Show |
55 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.242+2396G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53968147 | |||||||
chr2:53968274 | C | CA | 121 | a0001c0001t0001g0053 a0001c0001t0001g0305 a0001c0022t0016g0111 others(118): Show |
121 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.242+2268dupT | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53968274 | |||||||
chr2:53968334 | T | C | 1 | a0001c0007t0001g0179 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.242+2209A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53968334 | |||||||
chr2:53968424 | G | T | 1 | a0016c0024t0001g0312 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.242+2119C>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53968424 | |||||||
chr2:53968616 | T | C | 5 | a0001c0006t0005g0002 a0001c0006t0005g0003 a0001c0006t0005g0004 others(2): Show |
5 | HG02109.hp1 HG02145.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.242+1927A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53968616 | |||||||
chr2:53968877 | T | C | 240 | a0001c0001t0001g0053 a0001c0001t0001g0173 a0001c0005t0001g0311 others(237): Show |
240 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.242+1666A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53968877 | |||||||
chr2:53969013 | T | C | 1 | a0002c0002t0002g0153 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.242+1530A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53969013 | |||||||
chr2:53969101 | G | A | 127 | a0001c0001t0001g0053 a0001c0007t0001g0015 a0001c0007t0001g0017 others(124): Show |
127 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.242+1442C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53969101 | |||||||
chr2:53969149 | T | C | 1 | a0004c0008t0001g0383 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.242+1394A>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53969149 | |||||||
chr2:53969247 | A | C | 1 | a0001c0001t0001g0181 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.242+1296T>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53969247 | |||||||
chr2:53969410 | G | A | 1 | a0001c0001t0001g0308 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.242+1133C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53969410 | |||||||
chr2:53969412 | G | A | 1 | a0001c0001t0001g0308 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.242+1131C>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53969412 | |||||||
chr2:53969435 | A | G | 1 | a0001c0001t0001g0180 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.242+1108T>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53969435 | |||||||
chr2:53969635 | T | G | 73 | a0001c0005t0001g0311 a0001c0005t0001g0313 a0001c0005t0001g0314 others(70): Show |
73 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.242+908A>C | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53969635 | |||||||
chr2:53969660 | CT | C | 235 | a0001c0001t0001g0053 a0001c0001t0001g0173 a0001c0005t0001g0311 others(232): Show |
235 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.242+882delA | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53969660 | |||||||
chr2:53969672 | A | C | 32 | a0001c0001t0001g0173 a0001c0006t0003g0025 a0001c0006t0003g0026 others(29): Show |
32 | HG00099.hp2 HG00738.hp2 HG01099.hp2 others(29): Show |
intron_variant | MODIFIER | c.242+871T>G | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53969672 | |||||||
chr2:53969673 | C | A | 2 | a0001c0005t0001g0372 a0001c0005t0001g0373 |
2 | HG00408.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.242+870G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53969673 | |||||||
chr2:53969687 | G | GT | 136 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0038 others(133): Show |
136 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.242+855dupA | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53969687 | |||||||
chr2:53969687 | G | GTT | 11 | a0001c0007t0001g0015 a0001c0007t0001g0017 a0001c0007t0006g0012 others(8): Show |
11 | HG01081.hp2 HG01192.hp2 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.242+854_242+855dup others(2): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53969687 | |||||||
chr2:53969687 | G | T | 1 | a0002c0002t0002g0154 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.242+856C>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53969687 | |||||||
chr2:53969687 | GT | G | 74 | a0001c0005t0001g0313 a0001c0005t0001g0314 a0001c0005t0001g0315 others(71): Show |
74 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.242+855delA | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53969687 | |||||||
chr2:53969749 | A | T | 3 | a0001c0007t0006g0012 a0001c0007t0006g0014 a0014c0026t0001g0013 |
3 | HG02559.hp2 HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.242+794T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53969749 | |||||||
chr2:53969808 | C | T | 1 | a0002c0003t0002g0011 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.242+735G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53969808 | |||||||
chr2:53969916 | C | CTTAAGAT others(2): Show |
4 | a0001c0006t0005g0002 a0001c0006t0005g0003 a0001c0006t0005g0004 others(1): Show |
4 | HG02109.hp1 HG02145.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.242+626_242+627ins others(9): Show |
PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53969916 | |||||||
chr2:53969917 | A | T | 4 | a0001c0006t0005g0002 a0001c0006t0005g0003 a0001c0006t0005g0004 others(1): Show |
4 | HG02109.hp1 HG02145.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.242+626T>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53969917 | |||||||
chr2:53969989 | C | A | 72 | a0001c0005t0001g0311 a0001c0005t0001g0313 a0001c0005t0001g0314 others(69): Show |
72 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.242+554G>T | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53969989 | |||||||
chr2:53970390 | C | T | 1 | a0001c0001t0001g0010 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.242+153G>A | PSME4 | ENSG00000068878.15 | transcript | ENST00000404125.6 | protein_coding | 1/46 | chr2 | 53970390 |