Item | Value |
---|---|
geneid | 4134 |
ensemblid | ENSG00000047849.22 |
hgncid | 6862 |
symbol | MAP4 |
name | microtubule associated protein 4 |
refseq_nuc | NM_001385682.1 |
refseq_prot | NP_001372611.1 |
ensembl_nuc | ENST00000683076.1 |
ensembl_prot | ENSP00000507895.1 |
mane_status | MANE Select |
chr | chr3 |
start | 47850695 |
end | 48016416 |
strand | - |
ver | v1.2 |
region | chr3:47850695-48016416 |
region5000 | chr3:47845695-48021416 |
regionname0 | MAP4_chr3_47850695_48016416 |
regionname5000 | MAP4_chr3_47845695_48021416 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 2296 | 96 | 20 | 18 | 41 | 4 | 12 | 32 | MAP4_chr3_47845695_48021416 | MAP4 | MADLS others(2291): Show |
chr3 | 47845695 | 48021416 |
a0002 | 0/1 | 2296 | 68 | 11 | 16 | 36 | 2 | 2 | 30 | MAP4_chr3_47845695_48021416 | MAP4 | MADLS others(2291): Show |
chr3 | 47845695 | 48021416 |
a0003 | 0/0 | 2296 | 13 | 12 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | MADLS others(2291): Show |
chr3 | 47845695 | 48021416 |
a0004 | 0/0 | 2296 | 9 | 4 | 1 | 3 | 0 | 1 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | MADLS others(2291): Show |
chr3 | 47845695 | 48021416 |
a0005 | 0/0 | 2296 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | MADLS others(2291): Show |
chr3 | 47845695 | 48021416 |
a0006 | 0/0 | 2296 | 6 | 0 | 1 | 0 | 0 | 5 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | MADLS others(2291): Show |
chr3 | 47845695 | 48021416 |
a0007 | 0/0 | 2296 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | MADLS others(2291): Show |
chr3 | 47845695 | 48021416 |
a0008 | 0/0 | 2296 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | MADLS others(2291): Show |
chr3 | 47845695 | 48021416 |
a0009 | 0/0 | 2296 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | MADLS others(2291): Show |
chr3 | 47845695 | 48021416 |
a0010 | 0/0 | 2296 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | MADLS others(2291): Show |
chr3 | 47845695 | 48021416 |
a0011 | 0/0 | 2296 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | MADLS others(2291): Show |
chr3 | 47845695 | 48021416 |
a0012 | 0/0 | 2296 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | MADLS others(2291): Show |
chr3 | 47845695 | 48021416 |
a0013 | 0/0 | 2296 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | MAP4_chr3_47845695_48021416 | MAP4 | MADLS others(2291): Show |
chr3 | 47845695 | 48021416 |
a0014 | 0/0 | 2296 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | MADLS others(2291): Show |
chr3 | 47845695 | 48021416 |
a0015 | 0/0 | 2296 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | MADLS others(2291): Show |
chr3 | 47845695 | 48021416 |
a0016 | 0/0 | 2296 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | MADLS others(2291): Show |
chr3 | 47845695 | 48021416 |
a0017 | 0/0 | 2296 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | MADLS others(2291): Show |
chr3 | 47845695 | 48021416 |
a0018 | 0/0 | 2296 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | MADLS others(2291): Show |
chr3 | 47845695 | 48021416 |
a0019 | 0/0 | 2296 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | MADLS others(2291): Show |
chr3 | 47845695 | 48021416 |
a0020 | 0/0 | 2296 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | MADLS others(2291): Show |
chr3 | 47845695 | 48021416 |
a0021 | 0/0 | 2296 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | MADLS others(2291): Show |
chr3 | 47845695 | 48021416 |
a0022 | 0/0 | 2296 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | MADLS others(2291): Show |
chr3 | 47845695 | 48021416 |
a0023 | 0/0 | 2296 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | MADLS others(2291): Show |
chr3 | 47845695 | 48021416 |
a0024 | 0/0 | 2296 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | MADLS others(2291): Show |
chr3 | 47845695 | 48021416 |
a0025 | 0/0 | 2296 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | MADLS others(2291): Show |
chr3 | 47845695 | 48021416 |
a0026 | 0/0 | 2296 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | MADLS others(2291): Show |
chr3 | 47845695 | 48021416 |
a0027 | 0/0 | 2296 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | MADLS others(2291): Show |
chr3 | 47845695 | 48021416 |
a0028 | 0/0 | 2296 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | MADLS others(2291): Show |
chr3 | 47845695 | 48021416 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 6888 | 91 | 16 | 18 | 41 | 3 | 12 | MAP4_chr3_47845695_48021416 | MAP4 | ATGGC others(6883): Show |
chr3 | 47845695 | 48021416 | ||
a0001c0007 | 0/0 | 6888 | 4 | 4 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | ATGGC others(6883): Show |
chr3 | 47845695 | 48021416 | ||
a0001c0024 | 0/0 | 6888 | 1 | 0 | 0 | 0 | 1 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | ATGGC others(6883): Show |
chr3 | 47845695 | 48021416 | ||
a0002c0002 | 0/1 | 6888 | 65 | 10 | 14 | 36 | 2 | 2 | MAP4_chr3_47845695_48021416 | MAP4 | ATGGC others(6883): Show |
chr3 | 47845695 | 48021416 | ||
a0002c0011 | 0/0 | 6888 | 2 | 0 | 2 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | ATGGC others(6883): Show |
chr3 | 47845695 | 48021416 | ||
a0002c0020 | 0/0 | 6888 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | ATGGC others(6883): Show |
chr3 | 47845695 | 48021416 | ||
a0003c0003 | 0/0 | 6888 | 13 | 12 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | ATGGC others(6883): Show |
chr3 | 47845695 | 48021416 | ||
a0004c0004 | 0/0 | 6888 | 9 | 4 | 1 | 3 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | ATGGC others(6883): Show |
chr3 | 47845695 | 48021416 | ||
a0005c0005 | 0/0 | 6888 | 7 | 7 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | ATGGC others(6883): Show |
chr3 | 47845695 | 48021416 | ||
a0006c0006 | 0/0 | 6888 | 6 | 0 | 1 | 0 | 0 | 5 | MAP4_chr3_47845695_48021416 | MAP4 | ATGGC others(6883): Show |
chr3 | 47845695 | 48021416 | ||
a0007c0008 | 0/0 | 6888 | 4 | 4 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | ATGGC others(6883): Show |
chr3 | 47845695 | 48021416 | ||
a0008c0010 | 0/0 | 6888 | 3 | 2 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | ATGGC others(6883): Show |
chr3 | 47845695 | 48021416 | ||
a0009c0009 | 0/0 | 6888 | 3 | 3 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | ATGGC others(6883): Show |
chr3 | 47845695 | 48021416 | ||
a0010c0013 | 0/0 | 6888 | 2 | 2 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | ATGGC others(6883): Show |
chr3 | 47845695 | 48021416 | ||
a0011c0015 | 0/0 | 6888 | 2 | 2 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | ATGGC others(6883): Show |
chr3 | 47845695 | 48021416 | ||
a0012c0012 | 0/0 | 6888 | 2 | 0 | 0 | 0 | 0 | 2 | MAP4_chr3_47845695_48021416 | MAP4 | ATGGC others(6883): Show |
chr3 | 47845695 | 48021416 | ||
a0013c0014 | 0/0 | 6888 | 2 | 0 | 0 | 2 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | ATGGC others(6883): Show |
chr3 | 47845695 | 48021416 | ||
a0014c0025 | 0/0 | 6888 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | ATGGC others(6883): Show |
chr3 | 47845695 | 48021416 | ||
a0015c0021 | 0/0 | 6888 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | ATGGC others(6883): Show |
chr3 | 47845695 | 48021416 | ||
a0016c0027 | 0/0 | 6888 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | ATGGC others(6883): Show |
chr3 | 47845695 | 48021416 | ||
a0017c0026 | 0/0 | 6888 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | ATGGC others(6883): Show |
chr3 | 47845695 | 48021416 | ||
a0018c0016 | 0/0 | 6888 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | ATGGC others(6883): Show |
chr3 | 47845695 | 48021416 | ||
a0019c0018 | 0/0 | 6888 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | ATGGC others(6883): Show |
chr3 | 47845695 | 48021416 | ||
a0020c0023 | 0/0 | 6888 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | ATGGC others(6883): Show |
chr3 | 47845695 | 48021416 | ||
a0021c0028 | 0/0 | 6888 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | ATGGC others(6883): Show |
chr3 | 47845695 | 48021416 | ||
a0022c0030 | 0/0 | 6888 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | ATGGC others(6883): Show |
chr3 | 47845695 | 48021416 | ||
a0023c0022 | 0/0 | 6888 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | ATGGC others(6883): Show |
chr3 | 47845695 | 48021416 | ||
a0024c0029 | 0/0 | 6888 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | ATGGC others(6883): Show |
chr3 | 47845695 | 48021416 | ||
a0025c0031 | 0/0 | 6888 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | ATGGC others(6883): Show |
chr3 | 47845695 | 48021416 | ||
a0026c0019 | 0/0 | 6888 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | ATGGC others(6883): Show |
chr3 | 47845695 | 48021416 | ||
a0027c0032 | 0/0 | 6888 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | ATGGC others(6883): Show |
chr3 | 47845695 | 48021416 | ||
a0028c0017 | 0/0 | 6888 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | ATGGC others(6883): Show |
chr3 | 47845695 | 48021416 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 9232 | 82 | 10 | 17 | 40 | 3 | 11 | MAP4_chr3_47845695_48021416 | MAP4 | ATTTG others(9227): Show |
chr3 | 47845695 | 48021416 |
a0001c0001t0002 | 0/0 | 9235 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | ATTTG others(9230): Show |
chr3 | 47845695 | 48021416 |
a0001c0001t0008 | 0/0 | 9232 | 2 | 2 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | ATTTG others(9227): Show |
chr3 | 47845695 | 48021416 |
a0001c0001t0009 | 0/0 | 9235 | 2 | 2 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | ATTTG others(9230): Show |
chr3 | 47845695 | 48021416 |
a0001c0001t0012 | 0/0 | 9232 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | ATTTG others(9227): Show |
chr3 | 47845695 | 48021416 |
a0001c0001t0016 | 0/0 | 9232 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | ATTTG others(9227): Show |
chr3 | 47845695 | 48021416 |
a0001c0001t0022 | 0/0 | 9232 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | ATTTG others(9227): Show |
chr3 | 47845695 | 48021416 |
a0001c0001t0024 | 0/0 | 9232 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | ATTTG others(9227): Show |
chr3 | 47845695 | 48021416 |
a0001c0007t0001 | 0/0 | 9232 | 4 | 4 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | ATTTG others(9227): Show |
chr3 | 47845695 | 48021416 |
a0001c0024t0001 | 0/0 | 9232 | 1 | 0 | 0 | 0 | 1 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | ATTTG others(9227): Show |
chr3 | 47845695 | 48021416 |
a0002c0002t0002 | 0/1 | 9235 | 51 | 9 | 12 | 26 | 2 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | ATTTG others(9230): Show |
chr3 | 47845695 | 48021416 |
a0002c0002t0004 | 0/0 | 9235 | 9 | 0 | 0 | 9 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | ATTTG others(9230): Show |
chr3 | 47845695 | 48021416 |
a0002c0002t0005 | 0/0 | 9235 | 3 | 1 | 2 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | ATTTG others(9230): Show |
chr3 | 47845695 | 48021416 |
a0002c0002t0013 | 0/0 | 9235 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | ATTTG others(9230): Show |
chr3 | 47845695 | 48021416 |
a0002c0002t0019 | 0/0 | 9235 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | ATTTG others(9230): Show |
chr3 | 47845695 | 48021416 |
a0002c0011t0002 | 0/0 | 9235 | 2 | 0 | 2 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | ATTTG others(9230): Show |
chr3 | 47845695 | 48021416 |
a0002c0020t0002 | 0/0 | 9235 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | ATTTG others(9230): Show |
chr3 | 47845695 | 48021416 |
a0003c0003t0003 | 0/0 | 9235 | 12 | 11 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | ATTTG others(9230): Show |
chr3 | 47845695 | 48021416 |
a0003c0003t0021 | 0/0 | 9235 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | ATTTG others(9230): Show |
chr3 | 47845695 | 48021416 |
a0004c0004t0002 | 0/0 | 9235 | 4 | 0 | 0 | 3 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | ATTTG others(9230): Show |
chr3 | 47845695 | 48021416 |
a0004c0004t0011 | 0/0 | 9235 | 2 | 2 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | ATTTG others(9230): Show |
chr3 | 47845695 | 48021416 |
a0004c0004t0017 | 0/0 | 9234 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | ATTTG others(9229): Show |
chr3 | 47845695 | 48021416 |
a0004c0004t0018 | 0/0 | 9234 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | ATTTG others(9229): Show |
chr3 | 47845695 | 48021416 |
a0004c0004t0020 | 0/0 | 9235 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | ATTTG others(9230): Show |
chr3 | 47845695 | 48021416 |
a0005c0005t0003 | 0/0 | 9235 | 7 | 7 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | ATTTG others(9230): Show |
chr3 | 47845695 | 48021416 |
a0006c0006t0002 | 0/0 | 9235 | 6 | 0 | 1 | 0 | 0 | 5 | MAP4_chr3_47845695_48021416 | MAP4 | ATTTG others(9230): Show |
chr3 | 47845695 | 48021416 |
a0007c0008t0006 | 0/0 | 9235 | 4 | 4 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | ATTTG others(9230): Show |
chr3 | 47845695 | 48021416 |
a0008c0010t0007 | 0/0 | 9235 | 3 | 2 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | ATTTG others(9230): Show |
chr3 | 47845695 | 48021416 |
a0009c0009t0002 | 0/0 | 9235 | 3 | 3 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | ATTTG others(9230): Show |
chr3 | 47845695 | 48021416 |
a0010c0013t0010 | 0/0 | 9235 | 2 | 2 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | ATTTG others(9230): Show |
chr3 | 47845695 | 48021416 |
a0011c0015t0003 | 0/0 | 9235 | 2 | 2 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | ATTTG others(9230): Show |
chr3 | 47845695 | 48021416 |
a0012c0012t0002 | 0/0 | 9235 | 2 | 0 | 0 | 0 | 0 | 2 | MAP4_chr3_47845695_48021416 | MAP4 | ATTTG others(9230): Show |
chr3 | 47845695 | 48021416 |
a0013c0014t0001 | 0/0 | 9232 | 2 | 0 | 0 | 2 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | ATTTG others(9227): Show |
chr3 | 47845695 | 48021416 |
a0014c0025t0001 | 0/0 | 9232 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | ATTTG others(9227): Show |
chr3 | 47845695 | 48021416 |
a0015c0021t0002 | 0/0 | 9235 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | ATTTG others(9230): Show |
chr3 | 47845695 | 48021416 |
a0016c0027t0001 | 0/0 | 9232 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | ATTTG others(9227): Show |
chr3 | 47845695 | 48021416 |
a0017c0026t0014 | 0/0 | 9232 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | ATTTG others(9227): Show |
chr3 | 47845695 | 48021416 |
a0018c0016t0005 | 0/0 | 9235 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | ATTTG others(9230): Show |
chr3 | 47845695 | 48021416 |
a0019c0018t0002 | 0/0 | 9235 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | ATTTG others(9230): Show |
chr3 | 47845695 | 48021416 |
a0020c0023t0002 | 0/0 | 9235 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | ATTTG others(9230): Show |
chr3 | 47845695 | 48021416 |
a0021c0028t0002 | 0/0 | 9235 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | ATTTG others(9230): Show |
chr3 | 47845695 | 48021416 |
a0022c0030t0023 | 0/0 | 9234 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | ATTTG others(9229): Show |
chr3 | 47845695 | 48021416 |
a0023c0022t0002 | 0/0 | 9235 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | ATTTG others(9230): Show |
chr3 | 47845695 | 48021416 |
a0024c0029t0015 | 0/0 | 9232 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | ATTTG others(9227): Show |
chr3 | 47845695 | 48021416 |
a0025c0031t0003 | 0/0 | 9235 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | ATTTG others(9230): Show |
chr3 | 47845695 | 48021416 |
a0026c0019t0002 | 0/0 | 9235 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | ATTTG others(9230): Show |
chr3 | 47845695 | 48021416 |
a0027c0032t0002 | 0/0 | 9235 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | ATTTG others(9230): Show |
chr3 | 47845695 | 48021416 |
a0028c0017t0002 | 0/0 | 9235 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | ATTTG others(9230): Show |
chr3 | 47845695 | 48021416 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0124 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0008g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0008g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0009g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0009g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0012g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0016g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0022g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0001t0024g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0007t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0007t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0007t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0007t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0001c0024t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0070 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0004g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0004g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0004g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0004g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0004g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0004g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0004g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0004g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0004g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0005g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0005g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0005g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0013g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0002t0019g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0011t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0011t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0002c0020t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0003c0003t0003g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0003c0003t0003g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0003c0003t0003g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0003c0003t0003g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0003c0003t0003g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0003c0003t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0003c0003t0003g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0003c0003t0003g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0003c0003t0003g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0003c0003t0003g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0003c0003t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0003c0003t0003g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0003c0003t0021g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0004c0004t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0004c0004t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0004c0004t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0004c0004t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0004c0004t0011g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0004c0004t0011g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0004c0004t0017g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0004c0004t0018g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0004c0004t0020g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0005c0005t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0005c0005t0003g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0005c0005t0003g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0005c0005t0003g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0005c0005t0003g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0005c0005t0003g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0005c0005t0003g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0006c0006t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0006c0006t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0006c0006t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0006c0006t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0006c0006t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0006c0006t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0007c0008t0006g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0007c0008t0006g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0007c0008t0006g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0007c0008t0006g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0008c0010t0007g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0008c0010t0007g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0008c0010t0007g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0009c0009t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0009c0009t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0009c0009t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0010c0013t0010g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0010c0013t0010g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0011c0015t0003g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0011c0015t0003g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0012c0012t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0012c0012t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0013c0014t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0013c0014t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0014c0025t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0015c0021t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0016c0027t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0017c0026t0014g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0018c0016t0005g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0019c0018t0002g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0020c0023t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0021c0028t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0022c0030t0023g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0023c0022t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0024c0029t0015g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0025c0031t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0026c0019t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0027c0032t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
a0028c0017t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0194 | EUR | GBR | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG00099 | hp2 | a0002 | c0002 | t0002 | g0025 | EUR | GBR | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG00280 | hp1 | a0001 | c0024 | t0001 | g0133 | EUR | FIN | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG00280 | hp2 | a0002 | c0002 | t0002 | g0063 | EUR | FIN | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG00544 | hp1 | a0014 | c0025 | t0001 | g0215 | EAS | CHS | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG00544 | hp2 | a0002 | c0002 | t0002 | g0029 | EAS | CHS | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | CHS | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG00597 | hp2 | a0015 | c0021 | t0002 | g0011 | EAS | CHS | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | CHS | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | CHS | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG00639 | hp1 | a0002 | c0002 | t0002 | g0123 | AMR | PUR | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | CHS | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG00673 | hp2 | a0002 | c0002 | t0002 | g0022 | EAS | CHS | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG00733 | hp1 | a0002 | c0011 | t0002 | g0073 | AMR | PUR | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG00735 | hp1 | a0002 | c0002 | t0002 | g0012 | AMR | PUR | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG00735 | hp2 | a0016 | c0027 | t0001 | g0175 | AMR | PUR | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG00738 | hp1 | a0008 | c0010 | t0007 | g0113 | AMR | PUR | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG00741 | hp2 | a0002 | c0002 | t0002 | g0231 | AMR | PUR | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG01074 | hp2 | a0002 | c0002 | t0005 | g0040 | AMR | PUR | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG01099 | hp1 | a0002 | c0002 | t0002 | g0068 | AMR | PUR | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG01109 | hp2 | a0003 | c0003 | t0003 | g0095 | AMR | PUR | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG01169 | hp2 | a0002 | c0002 | t0002 | g0061 | AMR | PUR | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | CLM | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG01255 | hp2 | a0002 | c0011 | t0002 | g0087 | AMR | CLM | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG01257 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | CLM | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | CLM | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | CLM | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG01258 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | CLM | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG01346 | hp1 | a0017 | c0026 | t0014 | g0148 | AMR | CLM | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG01346 | hp2 | a0018 | c0016 | t0005 | g0031 | AMR | CLM | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG01496 | hp1 | a0002 | c0002 | t0005 | g0028 | AMR | CLM | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG01496 | hp2 | a0019 | c0018 | t0002 | g0023 | AMR | CLM | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0067 | EUR | IBS | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0158 | EUR | IBS | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG01884 | hp1 | a0005 | c0005 | t0003 | g0117 | AFR | ACB | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | ACB | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG01891 | hp1 | a0007 | c0008 | t0006 | g0149 | AFR | ACB | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG01891 | hp2 | a0009 | c0009 | t0002 | g0047 | AFR | ACB | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG01934 | hp1 | a0004 | c0004 | t0020 | g0080 | AMR | PEL | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | PEL | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG01943 | hp1 | a0002 | c0002 | t0002 | g0021 | AMR | PEL | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PEL | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG01981 | hp2 | a0002 | c0002 | t0002 | g0066 | AMR | PEL | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02015 | hp2 | a0002 | c0002 | t0002 | g0052 | EAS | KHV | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02040 | hp1 | a0002 | c0002 | t0019 | g0064 | EAS | KHV | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02040 | hp2 | a0004 | c0004 | t0002 | g0223 | EAS | KHV | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | ACB | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02055 | hp2 | a0003 | c0003 | t0003 | g0107 | AFR | ACB | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | KHV | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02071 | hp2 | a0020 | c0023 | t0002 | g0053 | EAS | KHV | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02083 | hp2 | a0004 | c0004 | t0002 | g0083 | EAS | KHV | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02135 | hp1 | a0002 | c0002 | t0002 | g0039 | EAS | KHV | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | KHV | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02145 | hp1 | a0002 | c0002 | t0002 | g0130 | AFR | ACB | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02145 | hp2 | a0021 | c0028 | t0002 | g0224 | AFR | ACB | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02148 | hp2 | a0002 | c0002 | t0002 | g0024 | AMR | PEL | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02258 | hp1 | a0009 | c0009 | t0002 | g0048 | AFR | ACB | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02258 | hp2 | a0001 | c0001 | t0008 | g0167 | AFR | ACB | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02273 | hp1 | a0002 | c0002 | t0002 | g0010 | AMR | PEL | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0150 | AMR | PEL | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02280 | hp1 | a0001 | c0001 | t0009 | g0205 | AFR | ACB | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02280 | hp2 | a0005 | c0005 | t0003 | g0115 | AFR | ACB | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02300 | hp1 | a0002 | c0002 | t0002 | g0051 | AMR | PEL | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | PEL | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02451 | hp1 | a0001 | c0007 | t0001 | g0221 | AFR | ACB | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02451 | hp2 | a0010 | c0013 | t0010 | g0002 | AFR | ACB | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02572 | hp1 | a0001 | c0007 | t0001 | g0219 | AFR | GWD | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02572 | hp2 | a0002 | c0002 | t0002 | g0056 | AFR | GWD | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02602 | hp1 | a0006 | c0006 | t0002 | g0075 | SAS | PJL | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02602 | hp2 | a0001 | c0001 | t0012 | g0204 | SAS | PJL | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02615 | hp2 | a0002 | c0002 | t0002 | g0069 | AFR | GWD | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02630 | hp1 | a0003 | c0003 | t0003 | g0098 | AFR | GWD | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | GWD | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02647 | hp1 | a0023 | c0022 | t0002 | g0088 | AFR | GWD | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02647 | hp2 | a0001 | c0007 | t0001 | g0220 | AFR | GWD | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02698 | hp2 | a0006 | c0006 | t0002 | g0062 | SAS | PJL | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | GWD | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02717 | hp2 | a0011 | c0015 | t0003 | g0096 | AFR | GWD | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02723 | hp1 | a0005 | c0005 | t0003 | g0121 | AFR | GWD | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02723 | hp2 | a0002 | c0020 | t0002 | g0054 | AFR | GWD | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02735 | hp1 | a0002 | c0002 | t0002 | g0032 | SAS | PJL | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02735 | hp2 | a0024 | c0029 | t0015 | g0155 | SAS | PJL | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02738 | hp2 | a0006 | c0006 | t0002 | g0076 | SAS | PJL | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02886 | hp1 | a0005 | c0005 | t0003 | g0119 | AFR | GWD | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02886 | hp2 | a0011 | c0015 | t0003 | g0097 | AFR | GWD | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02922 | hp1 | a0003 | c0003 | t0003 | g0110 | AFR | ESN | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02922 | hp2 | a0010 | c0013 | t0010 | g0222 | AFR | ESN | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | ESN | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02965 | hp2 | a0003 | c0003 | t0003 | g0104 | AFR | ESN | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02970 | hp1 | a0007 | c0008 | t0006 | g0152 | AFR | ESN | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02970 | hp2 | a0025 | c0031 | t0003 | g0109 | AFR | ESN | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02976 | hp1 | a0003 | c0003 | t0003 | g0101 | AFR | ESN | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02976 | hp2 | a0002 | c0002 | t0002 | g0125 | AFR | ESN | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG03041 | hp1 | a0003 | c0003 | t0003 | g0100 | AFR | GWD | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG03041 | hp2 | a0004 | c0004 | t0011 | g0049 | AFR | GWD | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG03098 | hp1 | a0002 | c0002 | t0002 | g0055 | AFR | MSL | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG03098 | hp2 | a0009 | c0009 | t0002 | g0046 | AFR | MSL | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | ESN | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG03139 | hp2 | a0003 | c0003 | t0003 | g0102 | AFR | ESN | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG03225 | hp1 | a0005 | c0005 | t0003 | g0114 | AFR | MSL | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG03225 | hp2 | a0003 | c0003 | t0003 | g0099 | AFR | MSL | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG03453 | hp1 | a0004 | c0004 | t0011 | g0050 | AFR | MSL | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG03453 | hp2 | a0004 | c0004 | t0017 | g0086 | AFR | MSL | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG03486 | hp1 | a0003 | c0003 | t0003 | g0103 | AFR | MSL | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG03486 | hp2 | a0008 | c0010 | t0007 | g0112 | AFR | MSL | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG03491 | hp1 | a0004 | c0004 | t0002 | g0084 | SAS | PJL | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG03516 | hp1 | a0003 | c0003 | t0003 | g0108 | AFR | ESN | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG03516 | hp2 | a0001 | c0001 | t0024 | g0165 | AFR | ESN | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG03540 | hp1 | a0002 | c0002 | t0002 | g0045 | AFR | GWD | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG03540 | hp2 | a0001 | c0007 | t0001 | g0218 | AFR | GWD | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG03579 | hp1 | a0002 | c0002 | t0002 | g0058 | AFR | MSL | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG03579 | hp2 | a0003 | c0003 | t0003 | g0106 | AFR | MSL | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0156 | SAS | BEB | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG03831 | hp2 | a0006 | c0006 | t0002 | g0074 | SAS | BEB | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG03834 | hp1 | a0006 | c0006 | t0002 | g0079 | SAS | BEB | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | BEB | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | BEB | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG03927 | hp2 | a0002 | c0002 | t0013 | g0065 | SAS | BEB | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0191 | SAS | STU | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG04115 | hp2 | a0012 | c0012 | t0002 | g0078 | SAS | STU | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG04204 | hp1 | a0026 | c0019 | t0002 | g0077 | SAS | STU | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0192 | SAS | STU | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0193 | SAS | STU | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG04228 | hp2 | a0012 | c0012 | t0002 | g0071 | SAS | STU | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA18522 | hp1 | a0027 | c0032 | t0002 | g0059 | AFR | YRI | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA18522 | hp2 | a0001 | c0001 | t0016 | g0135 | AFR | YRI | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA18747 | hp1 | a0002 | c0002 | t0002 | g0118 | EAS | CHB | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | CHB | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA18940 | hp1 | a0002 | c0002 | t0002 | g0035 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA18941 | hp1 | a0002 | c0002 | t0002 | g0091 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA18942 | hp2 | a0002 | c0002 | t0004 | g0003 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA18943 | hp2 | a0002 | c0002 | t0002 | g0089 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA18946 | hp1 | a0002 | c0002 | t0002 | g0037 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA18952 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA18953 | hp1 | a0002 | c0002 | t0004 | g0019 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA18956 | hp1 | a0002 | c0002 | t0004 | g0017 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA18961 | hp1 | a0002 | c0002 | t0004 | g0007 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA18963 | hp2 | a0002 | c0002 | t0002 | g0033 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA18967 | hp2 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA18969 | hp2 | a0028 | c0017 | t0002 | g0038 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA18970 | hp2 | a0002 | c0002 | t0002 | g0092 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA18973 | hp1 | a0002 | c0002 | t0002 | g0036 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA18998 | hp1 | a0002 | c0002 | t0002 | g0090 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA18999 | hp2 | a0002 | c0002 | t0004 | g0008 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA19000 | hp1 | a0004 | c0004 | t0002 | g0085 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA19000 | hp2 | a0002 | c0002 | t0002 | g0030 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA19004 | hp1 | a0002 | c0002 | t0002 | g0014 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA19005 | hp2 | a0002 | c0002 | t0004 | g0015 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA19006 | hp1 | a0002 | c0002 | t0002 | g0120 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA19006 | hp2 | a0001 | c0001 | t0022 | g0213 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA19007 | hp1 | a0013 | c0014 | t0001 | g0143 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA19007 | hp2 | a0002 | c0002 | t0004 | g0016 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA19012 | hp1 | a0002 | c0002 | t0002 | g0013 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA19030 | hp1 | a0001 | c0001 | t0009 | g0178 | AFR | LWK | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA19030 | hp2 | a0002 | c0002 | t0005 | g0026 | AFR | LWK | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | LWK | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA19043 | hp2 | a0002 | c0002 | t0002 | g0082 | AFR | LWK | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA19058 | hp2 | a0002 | c0002 | t0002 | g0072 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA19065 | hp2 | a0002 | c0002 | t0002 | g0027 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA19067 | hp2 | a0002 | c0002 | t0002 | g0018 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA19079 | hp1 | a0002 | c0002 | t0002 | g0034 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA19082 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA19086 | hp2 | a0002 | c0002 | t0002 | g0093 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA19087 | hp1 | a0002 | c0002 | t0002 | g0094 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA19088 | hp1 | a0002 | c0002 | t0004 | g0009 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA19091 | hp1 | a0013 | c0014 | t0001 | g0142 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA19091 | hp2 | a0002 | c0002 | t0004 | g0006 | EAS | JPT | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA19240 | hp1 | a0007 | c0008 | t0006 | g0226 | AFR | YRI | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | YRI | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA20129 | hp1 | a0003 | c0003 | t0021 | g0105 | AFR | ASW | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA20129 | hp2 | a0008 | c0010 | t0007 | g0111 | AFR | ASW | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | CLM | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG01123 | hp2 | a0006 | c0006 | t0002 | g0081 | AMR | CLM | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02486 | hp1 | a0022 | c0030 | t0023 | g0044 | AFR | ACB | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02486 | hp2 | a0004 | c0004 | t0018 | g0060 | AFR | ACB | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02559 | hp1 | a0002 | c0002 | t0002 | g0057 | AFR | ACB | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | ACB | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG03471 | hp1 | a0001 | c0001 | t0008 | g0166 | AFR | MSL | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
HG03471 | hp2 | a0005 | c0005 | t0003 | g0116 | AFR | MSL | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA20300 | hp1 | a0007 | c0008 | t0006 | g0131 | AFR | USA | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
NA20300 | hp2 | a0005 | c0005 | t0003 | g0122 | AFR | USA | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
homoSapiens | chm13v2 | a0002 | c0002 | t0002 | g0070 | REF | REF | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0124 | REF | REF | MAP4_chr3_47845695_48021416 | MAP4 | chr3 | 47845695 | 48021416 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:47877426 | C | A | 1 | a0025 | 1 | HG02970.hp2 | missense_variant | MODERATE | c.5532G>T | p.Lys1844Asn | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 11/21 | 5634/9232 | 5532/6891 | 1844/2296 | chr3 | 47877426 | |||
chr3:47909184 | G | C | 1 | a0009 | 3 | HG01891.hp2 HG02258.hp1 HG03098.hp2 |
missense_variant | MODERATE | c.5237C>G | p.Pro1746Arg | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/21 | 5339/9232 | 5237/6891 | 1746/2296 | chr3 | 47909184 | |||
chr3:47909809 | T | C | 1 | a0028 | 1 | NA18969.hp2 | missense_variant | MODERATE | c.4612A>G | p.Lys1538Glu | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/21 | 4714/9232 | 4612/6891 | 1538/2296 | chr3 | 47909809 | |||
chr3:47909913 | G | A | 1 | a0019 | 1 | HG01496.hp2 | missense_variant | MODERATE | c.4508C>T | p.Thr1503Ile | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/21 | 4610/9232 | 4508/6891 | 1503/2296 | chr3 | 47909913 | |||
chr3:47910180 | A | G | 1 | a0009 | 3 | HG01891.hp2 HG02258.hp1 HG03098.hp2 |
missense_variant | MODERATE | c.4241T>C | p.Ile1414Thr | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/21 | 4343/9232 | 4241/6891 | 1414/2296 | chr3 | 47910180 | |||
chr3:47910484 | T | C | 1 | a0026 | 1 | HG04204.hp1 | missense_variant | MODERATE | c.3937A>G | p.Thr1313Ala | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/21 | 4039/9232 | 3937/6891 | 1313/2296 | chr3 | 47910484 | |||
chr3:47910660 | G | A | 1 | a0008 | 3 | HG00738.hp1 HG03486.hp2 NA20129.hp2 |
missense_variant | MODERATE | c.3761C>T | p.Pro1254Leu | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/21 | 3863/9232 | 3761/6891 | 1254/2296 | chr3 | 47910660 | |||
chr3:47910864 | T | C | 1 | a0015 | 1 | HG00597.hp2 | missense_variant | MODERATE | c.3557A>G | p.Asn1186Ser | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/21 | 3659/9232 | 3557/6891 | 1186/2296 | chr3 | 47910864 | |||
chr3:47911004 | C | T | 1 | a0007 | 4 | HG01891.hp1 HG02970.hp1 NA19240.hp1 others(1): Show |
missense_variant | MODERATE | c.3417G>A | p.Met1139Ile | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/21 | 3519/9232 | 3417/6891 | 1139/2296 | chr3 | 47911004 | |||
chr3:47911145 | C | G | 1 | a0013 | 2 | NA19007.hp1 NA19091.hp1 |
missense_variant | MODERATE | c.3276G>C | p.Lys1092Asn | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/21 | 3378/9232 | 3276/6891 | 1092/2296 | chr3 | 47911145 | |||
chr3:47911353 | T | C | 1 | a0003 | 13 | HG01109.hp2 HG02055.hp2 HG02630.hp1 others(10): Show |
missense_variant | MODERATE | c.3068A>G | p.Asn1023Ser | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/21 | 3170/9232 | 3068/6891 | 1023/2296 | chr3 | 47911353 | |||
chr3:47911716 | T | G | 1 | a0012 | 2 | HG04115.hp2 HG04228.hp2 |
missense_variant | MODERATE | c.2705A>C | p.Lys902Thr | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/21 | 2807/9232 | 2705/6891 | 902/2296 | chr3 | 47911716 | |||
chr3:47911750 | G | C | 1 | a0020 | 1 | HG02071.hp2 | missense_variant | MODERATE | c.2671C>G | p.Gln891Glu | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/21 | 2773/9232 | 2671/6891 | 891/2296 | chr3 | 47911750 | |||
chr3:47911915 | A | C | 21 | a0002 a0003 a0004 others(18): Show |
125 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(122): Show |
missense_variant | MODERATE | c.2506T>G | p.Leu836Val | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/21 | 2608/9232 | 2506/6891 | 836/2296 | chr3 | 47911915 | |||
chr3:47912067 | G | A | 1 | a0014 | 1 | HG00544.hp1 | missense_variant | MODERATE | c.2354C>T | p.Ala785Val | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/21 | 2456/9232 | 2354/6891 | 785/2296 | chr3 | 47912067 | |||
chr3:47912151 | T | A | 1 | a0023 | 1 | HG02647.hp1 | missense_variant | MODERATE | c.2270A>T | p.Glu757Val | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/21 | 2372/9232 | 2270/6891 | 757/2296 | chr3 | 47912151 | |||
chr3:47912243 | C | A | 11 | a0002 a0004 a0006 others(8): Show |
91 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(88): Show |
missense_variant | MODERATE | c.2178G>T | p.Trp726Cys | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/21 | 2280/9232 | 2178/6891 | 726/2296 | chr3 | 47912243 | |||
chr3:47912274 | A | G | 1 | a0018 | 1 | HG01346.hp2 | missense_variant | MODERATE | c.2147T>C | p.Leu716Pro | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/21 | 2249/9232 | 2147/6891 | 716/2296 | chr3 | 47912274 | |||
chr3:47912323 | G | A | 1 | a0011 | 2 | HG02717.hp2 HG02886.hp2 |
missense_variant | MODERATE | c.2098C>T | p.Pro700Ser | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/21 | 2200/9232 | 2098/6891 | 700/2296 | chr3 | 47912323 | |||
chr3:47914894 | T | C | 1 | a0017 | 1 | HG01346.hp1 | missense_variant | MODERATE | c.1922A>G | p.Glu641Gly | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 8/21 | 2024/9232 | 1922/6891 | 641/2296 | chr3 | 47914894 | |||
chr3:47914934 | C | T | 18 | a0002 a0003 a0004 others(15): Show |
121 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(118): Show |
missense_variant | MODERATE | c.1882G>A | p.Val628Ile | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 8/21 | 1984/9232 | 1882/6891 | 628/2296 | chr3 | 47914934 | |||
chr3:47915990 | C | T | 1 | a0021 | 1 | HG02145.hp2 | missense_variant | MODERATE | c.1837G>A | p.Val613Met | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 7/21 | 1939/9232 | 1837/6891 | 613/2296 | chr3 | 47915990 | |||
chr3:47916106 | T | G | 1 | a0016 | 1 | HG00735.hp2 | missense_variant | MODERATE | c.1721A>C | p.Lys574Thr | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 7/21 | 1823/9232 | 1721/6891 | 574/2296 | chr3 | 47916106 | |||
chr3:47916227 | C | T | 1 | a0022 | 1 | HG02486.hp1 | missense_variant | MODERATE | c.1600G>A | p.Val534Ile | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 7/21 | 1702/9232 | 1600/6891 | 534/2296 | chr3 | 47916227 | |||
chr3:47916506 | C | G | 1 | a0006 | 6 | HG01123.hp2 HG02602.hp1 HG02698.hp2 others(3): Show |
missense_variant | MODERATE | c.1321G>C | p.Glu441Gln | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 7/21 | 1423/9232 | 1321/6891 | 441/2296 | chr3 | 47916506 | |||
chr3:47916511 | G | A | 1 | a0024 | 1 | HG02735.hp2 | missense_variant | MODERATE | c.1316C>T | p.Ser439Phe | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 7/21 | 1418/9232 | 1316/6891 | 439/2296 | chr3 | 47916511 | |||
chr3:47916547 | G | T | 9 | a0002 a0006 a0012 others(6): Show |
81 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(78): Show |
missense_variant | MODERATE | c.1280C>A | p.Ser427Tyr | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 7/21 | 1382/9232 | 1280/6891 | 427/2296 | chr3 | 47916547 | |||
chr3:47917084 | G | C | 1 | a0022 | 1 | HG02486.hp1 | missense_variant | MODERATE | c.743C>G | p.Thr248Ser | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 7/21 | 845/9232 | 743/6891 | 248/2296 | chr3 | 47917084 | |||
chr3:47998684 | G | C | 1 | a0027 | 1 | NA18522.hp1 | missense_variant | MODERATE | c.177C>G | p.Asn59Lys | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/21 | 279/9232 | 177/6891 | 59/2296 | chr3 | 47998684 | |||
chr3:47998793 | C | T | 1 | a0006 | 6 | HG01123.hp2 HG02602.hp1 HG02698.hp2 others(3): Show |
missense_variant | MODERATE | c.68G>A | p.Arg23Gln | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/21 | 170/9232 | 68/6891 | 23/2296 | chr3 | 47998793 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:47872008 | C | T | 1 | a0002c0011 | 2 | HG00733.hp1 HG01255.hp2 |
synonymous_variant | LOW | c.5850G>A | p.Gln1950Gln | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 13/21 | 5952/9232 | 5850/6891 | 1950/2296 | chr3 | 47872008 | |||
chr3:47909144 | T | C | 1 | a0023c0022 | 1 | HG02647.hp1 | synonymous_variant | LOW | c.5277A>G | p.Glu1759Glu | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/21 | 5379/9232 | 5277/6891 | 1759/2296 | chr3 | 47909144 | |||
chr3:47910509 | G | A | 1 | a0002c0020 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.3912C>T | p.Asn1304Asn | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/21 | 4014/9232 | 3912/6891 | 1304/2296 | chr3 | 47910509 | |||
chr3:47911019 | C | T | 1 | a0001c0024 | 1 | HG00280.hp1 | synonymous_variant | LOW | c.3402G>A | p.Thr1134Thr | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/21 | 3504/9232 | 3402/6891 | 1134/2296 | chr3 | 47911019 | |||
chr3:47916180 | G | A | 1 | a0021c0028 | 1 | HG02145.hp2 | synonymous_variant | LOW | c.1647C>T | p.Val549Val | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 7/21 | 1749/9232 | 1647/6891 | 549/2296 | chr3 | 47916180 | |||
chr3:47928244 | G | A | 5 | a0003c0003 a0005c0005 a0008c0010 others(2): Show |
26 | HG00738.hp1 HG01109.hp2 HG01884.hp1 others(23): Show |
synonymous_variant | LOW | c.399C>T | p.Val133Val | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 4/21 | 501/9232 | 399/6891 | 133/2296 | chr3 | 47928244 | |||
chr3:47998750 | A | G | 1 | a0001c0007 | 4 | HG02451.hp1 HG02572.hp1 HG02647.hp2 others(1): Show |
synonymous_variant | LOW | c.111T>C | p.Val37Val | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/21 | 213/9232 | 111/6891 | 37/2296 | chr3 | 47998750 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:47850746 | G | C | 1 | a0002c0002t0019 | 1 | HG02040.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2188C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 21/21 | 2188 | chr3 | 47850746 | ||||||
chr3:47850886 | C | CCTT | 34 | a0001c0001t0002 a0001c0001t0009 a0002c0002t0002 others(31): Show |
128 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(125): Show |
3_prime_UTR_variant | MODIFIER | c.*2045_*2047dupAAG | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 21/21 | 2047 | chr3 | 47850886 | ||||||
chr3:47850893 | G | A | 6 | a0003c0003t0003 a0003c0003t0021 a0005c0005t0003 others(3): Show |
26 | HG00738.hp1 HG01109.hp2 HG01884.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*2041C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 21/21 | 2041 | chr3 | 47850893 | ||||||
chr3:47850932 | G | A | 1 | a0002c0002t0013 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2002C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 21/21 | 2002 | chr3 | 47850932 | ||||||
chr3:47850941 | G | T | 1 | a0017c0026t0014 | 1 | HG01346.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1993C>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 21/21 | 1993 | chr3 | 47850941 | ||||||
chr3:47851024 | A | AGAC | 1 | a0007c0008t0006 | 4 | HG01891.hp1 HG02970.hp1 NA19240.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1907_*1909dupGTC | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 21/21 | 1909 | chr3 | 47851024 | ||||||
chr3:47851084 | A | T | 1 | a0001c0001t0008 | 2 | HG02258.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1850T>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 21/21 | 1850 | chr3 | 47851084 | ||||||
chr3:47851089 | G | C | 33 | a0001c0001t0002 a0002c0002t0002 a0002c0002t0004 others(30): Show |
126 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(123): Show |
3_prime_UTR_variant | MODIFIER | c.*1845C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 21/21 | 1845 | chr3 | 47851089 | ||||||
chr3:47851293 | G | A | 1 | a0004c0004t0017 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1641C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 21/21 | 1641 | chr3 | 47851293 | ||||||
chr3:47851365 | C | T | 2 | a0002c0002t0005 a0018c0016t0005 |
4 | HG01074.hp2 HG01346.hp2 HG01496.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1569G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 21/21 | 1569 | chr3 | 47851365 | ||||||
chr3:47851438 | G | A | 1 | a0008c0010t0007 | 3 | HG00738.hp1 HG03486.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1496C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 21/21 | 1496 | chr3 | 47851438 | ||||||
chr3:47851453 | T | C | 1 | a0022c0030t0023 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1481A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 21/21 | 1481 | chr3 | 47851453 | ||||||
chr3:47851764 | T | G | 2 | a0004c0004t0018 a0004c0004t0020 |
2 | HG01934.hp1 HG02486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1170A>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 21/21 | 1170 | chr3 | 47851764 | ||||||
chr3:47852373 | A | G | 1 | a0002c0002t0004 | 9 | NA18942.hp2 NA18953.hp1 NA18956.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*561T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 21/21 | 561 | chr3 | 47852373 | ||||||
chr3:47852378 | GA | G | 3 | a0004c0004t0017 a0004c0004t0018 a0022c0030t0023 |
3 | HG02486.hp1 HG02486.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*555delT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 21/21 | 555 | chr3 | 47852378 | ||||||
chr3:47852379 | A | G | 5 | a0004c0004t0002 a0004c0004t0011 a0004c0004t0020 others(2): Show |
9 | HG01934.hp1 HG02040.hp2 HG02071.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*555T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 21/21 | 555 | chr3 | 47852379 | ||||||
chr3:47852380 | G | C | 1 | a0004c0004t0011 | 2 | HG03041.hp2 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*554C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 21/21 | 554 | chr3 | 47852380 | ||||||
chr3:47852381 | G | A | 1 | a0003c0003t0021 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*553C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 21/21 | 553 | chr3 | 47852381 | ||||||
chr3:47852442 | T | A | 1 | a0001c0001t0022 | 1 | NA19006.hp2 | 3_prime_UTR_variant | MODIFIER | c.*492A>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 21/21 | 492 | chr3 | 47852442 | ||||||
chr3:47852451 | C | T | 1 | a0001c0001t0016 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*483G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 21/21 | 483 | chr3 | 47852451 | ||||||
chr3:47852556 | T | G | 1 | a0022c0030t0023 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*378A>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 21/21 | 378 | chr3 | 47852556 | ||||||
chr3:47852611 | C | T | 2 | a0017c0026t0014 a0024c0029t0015 |
2 | HG01346.hp1 HG02735.hp2 |
3_prime_UTR_variant | MODIFIER | c.*323G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 21/21 | 323 | chr3 | 47852611 | ||||||
chr3:47852661 | G | A | 2 | a0004c0004t0011 a0010c0013t0010 |
4 | HG02451.hp2 HG02922.hp2 HG03041.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*273C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 21/21 | 273 | chr3 | 47852661 | ||||||
chr3:47852728 | C | T | 2 | a0001c0001t0012 a0002c0002t0013 |
2 | HG02602.hp2 HG03927.hp2 |
3_prime_UTR_variant | MODIFIER | c.*206G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 21/21 | 206 | chr3 | 47852728 | ||||||
chr3:47852877 | T | A | 1 | a0001c0001t0024 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*57A>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 21/21 | 57 | chr3 | 47852877 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:47852998 | G | C | 1 | a0001c0001t0001g0172 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.6887-60C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 20/20 | chr3 | 47852998 | |||||||
chr3:47853391 | CGAG | C | 26 | a0002c0002t0002g0001 a0002c0002t0002g0037 a0002c0002t0002g0039 others(23): Show |
27 | HG00280.hp2 HG00741.hp2 HG01099.hp1 others(24): Show |
intron_variant | MODIFIER | c.6697-42_6697-40del others(3): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 19/20 | chr3 | 47853391 | |||||||
chr3:47853393 | A | G | 6 | a0006c0006t0002g0062 a0006c0006t0002g0074 a0006c0006t0002g0075 others(3): Show |
6 | HG01123.hp2 HG02602.hp1 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.6697-41T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 19/20 | chr3 | 47853393 | |||||||
chr3:47853394 | G | T | 35 | a0003c0003t0003g0095 a0003c0003t0003g0098 a0003c0003t0003g0099 others(32): Show |
35 | HG00738.hp1 HG01109.hp2 HG01884.hp1 others(32): Show |
intron_variant | MODIFIER | c.6697-42C>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 19/20 | chr3 | 47853394 | |||||||
chr3:47853396 | G | C | 1 | a0022c0030t0023g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.6697-44C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 19/20 | chr3 | 47853396 | |||||||
chr3:47853478 | C | T | 1 | a0001c0001t0009g0178 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.6697-126G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 19/20 | chr3 | 47853478 | |||||||
chr3:47853510 | G | A | 1 | a0028c0017t0002g0038 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.6697-158C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 19/20 | chr3 | 47853510 | |||||||
chr3:47853542 | G | A | 1 | a0023c0022t0002g0088 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.6697-190C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 19/20 | chr3 | 47853542 | |||||||
chr3:47853549 | G | A | 2 | a0002c0002t0002g0092 a0002c0002t0002g0093 |
2 | NA18970.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.6697-197C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 19/20 | chr3 | 47853549 | |||||||
chr3:47853851 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.6697-499C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 19/20 | chr3 | 47853851 | |||||||
chr3:47853913 | C | A | 16 | a0002c0002t0002g0004 a0002c0002t0002g0005 a0002c0002t0002g0012 others(13): Show |
16 | HG00099.hp2 HG00673.hp2 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.6697-561G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 19/20 | chr3 | 47853913 | |||||||
chr3:47854215 | C | T | 2 | a0002c0002t0002g0069 a0002c0002t0002g0231 |
2 | HG00741.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.6697-863G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 19/20 | chr3 | 47854215 | |||||||
chr3:47854312 | C | T | 2 | a0004c0004t0011g0049 a0004c0004t0011g0050 |
2 | HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.6696+936G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 19/20 | chr3 | 47854312 | |||||||
chr3:47854324 | C | T | 1 | a0004c0004t0002g0223 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.6696+924G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 19/20 | chr3 | 47854324 | |||||||
chr3:47854344 | C | T | 16 | a0003c0003t0003g0095 a0003c0003t0003g0098 a0003c0003t0003g0099 others(13): Show |
16 | HG01109.hp2 HG02055.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.6696+904G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 19/20 | chr3 | 47854344 | |||||||
chr3:47854465 | C | T | 4 | a0005c0005t0003g0114 a0005c0005t0003g0115 a0005c0005t0003g0116 others(1): Show |
4 | HG01884.hp1 HG02280.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.6696+783G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 19/20 | chr3 | 47854465 | |||||||
chr3:47854559 | A | G | 3 | a0010c0013t0010g0002 a0010c0013t0010g0222 a0021c0028t0002g0224 |
3 | HG02145.hp2 HG02451.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.6696+689T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 19/20 | chr3 | 47854559 | |||||||
chr3:47854680 | C | T | 1 | a0001c0007t0001g0219 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.6696+568G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 19/20 | chr3 | 47854680 | |||||||
chr3:47854720 | A | AGCCCTGC others(19): Show |
2 | a0007c0008t0006g0149 a0007c0008t0006g0152 |
2 | HG01891.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.6696+502_6696+527d others(28): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 19/20 | chr3 | 47854720 | |||||||
chr3:47854720 | AGCCCTGC others(19): Show |
A | 124 | a0002c0002t0002g0001 a0002c0002t0002g0004 a0002c0002t0002g0005 others(121): Show |
125 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.6696+502_6696+527d others(28): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 19/20 | chr3 | 47854720 | |||||||
chr3:47854899 | C | G | 1 | a0002c0002t0004g0009 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.6696+349G>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 19/20 | chr3 | 47854899 | |||||||
chr3:47854935 | C | G | 1 | a0001c0001t0001g0201 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.6696+313G>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 19/20 | chr3 | 47854935 | |||||||
chr3:47855036 | A | G | 1 | a0002c0002t0002g0022 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.6696+212T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 19/20 | chr3 | 47855036 | |||||||
chr3:47855877 | G | C | 1 | a0002c0002t0002g0231 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.6584-517C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 18/20 | chr3 | 47855877 | |||||||
chr3:47856379 | A | G | 1 | a0004c0004t0011g0049 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.6584-1019T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 18/20 | chr3 | 47856379 | |||||||
chr3:47856696 | G | A | 1 | a0002c0002t0002g0123 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.6583+735C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 18/20 | chr3 | 47856696 | |||||||
chr3:47856817 | A | G | 93 | a0002c0002t0002g0001 a0002c0002t0002g0027 a0002c0002t0002g0029 others(90): Show |
94 | HG00280.hp2 HG00544.hp2 HG00639.hp1 others(91): Show |
intron_variant | MODIFIER | c.6583+614T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 18/20 | chr3 | 47856817 | |||||||
chr3:47856982 | C | T | 3 | a0010c0013t0010g0002 a0010c0013t0010g0222 a0021c0028t0002g0224 |
3 | HG02145.hp2 HG02451.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.6583+449G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 18/20 | chr3 | 47856982 | |||||||
chr3:47857229 | A | G | 31 | a0002c0002t0002g0004 a0002c0002t0002g0005 a0002c0002t0002g0010 others(28): Show |
31 | HG00099.hp2 HG00597.hp2 HG00673.hp2 others(28): Show |
intron_variant | MODIFIER | c.6583+202T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 18/20 | chr3 | 47857229 | |||||||
chr3:47857334 | C | G | 1 | a0001c0001t0009g0178 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.6583+97G>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 18/20 | chr3 | 47857334 | |||||||
chr3:47857568 | AC | A | 7 | a0002c0002t0002g0027 a0002c0002t0002g0029 a0002c0002t0002g0030 others(4): Show |
7 | HG00544.hp2 HG02735.hp1 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.6502-57delG | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47857568 | |||||||
chr3:47857573 | A | T | 7 | a0002c0002t0002g0027 a0002c0002t0002g0029 a0002c0002t0002g0030 others(4): Show |
7 | HG00544.hp2 HG02735.hp1 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.6502-61T>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47857573 | |||||||
chr3:47857575 | G | T | 7 | a0002c0002t0002g0027 a0002c0002t0002g0029 a0002c0002t0002g0030 others(4): Show |
7 | HG00544.hp2 HG02735.hp1 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.6502-63C>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47857575 | |||||||
chr3:47857576 | C | T | 7 | a0002c0002t0002g0027 a0002c0002t0002g0029 a0002c0002t0002g0030 others(4): Show |
7 | HG00544.hp2 HG02735.hp1 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.6502-64G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47857576 | |||||||
chr3:47857579 | C | T | 7 | a0002c0002t0002g0027 a0002c0002t0002g0029 a0002c0002t0002g0030 others(4): Show |
7 | HG00544.hp2 HG02735.hp1 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.6502-67G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47857579 | |||||||
chr3:47857589 | C | A | 7 | a0002c0002t0002g0027 a0002c0002t0002g0029 a0002c0002t0002g0030 others(4): Show |
7 | HG00544.hp2 HG02735.hp1 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.6502-77G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47857589 | |||||||
chr3:47857590 | T | A | 7 | a0002c0002t0002g0027 a0002c0002t0002g0029 a0002c0002t0002g0030 others(4): Show |
7 | HG00544.hp2 HG02735.hp1 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.6502-78A>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47857590 | |||||||
chr3:47857592 | C | A | 7 | a0002c0002t0002g0027 a0002c0002t0002g0029 a0002c0002t0002g0030 others(4): Show |
7 | HG00544.hp2 HG02735.hp1 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.6502-80G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47857592 | |||||||
chr3:47857593 | T | A | 7 | a0002c0002t0002g0027 a0002c0002t0002g0029 a0002c0002t0002g0030 others(4): Show |
7 | HG00544.hp2 HG02735.hp1 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.6502-81A>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47857593 | |||||||
chr3:47857594 | C | A | 7 | a0002c0002t0002g0027 a0002c0002t0002g0029 a0002c0002t0002g0030 others(4): Show |
7 | HG00544.hp2 HG02735.hp1 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.6502-82G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47857594 | |||||||
chr3:47857595 | C | T | 7 | a0002c0002t0002g0027 a0002c0002t0002g0029 a0002c0002t0002g0030 others(4): Show |
7 | HG00544.hp2 HG02735.hp1 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.6502-83G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47857595 | |||||||
chr3:47857597 | T | A | 7 | a0002c0002t0002g0027 a0002c0002t0002g0029 a0002c0002t0002g0030 others(4): Show |
7 | HG00544.hp2 HG02735.hp1 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.6502-85A>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47857597 | |||||||
chr3:47857598 | G | A | 7 | a0002c0002t0002g0027 a0002c0002t0002g0029 a0002c0002t0002g0030 others(4): Show |
7 | HG00544.hp2 HG02735.hp1 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.6502-86C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47857598 | |||||||
chr3:47857599 | T | TAATAAAT others(67): Show |
7 | a0002c0002t0002g0027 a0002c0002t0002g0029 a0002c0002t0002g0030 others(4): Show |
7 | HG00544.hp2 HG02735.hp1 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.6502-88_6502-87ins others(74): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47857599 | |||||||
chr3:47858021 | C | CT | 99 | a0001c0001t0001g0200 a0001c0001t0001g0227 a0002c0002t0002g0001 others(96): Show |
100 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.6502-510dupA | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47858021 | |||||||
chr3:47858024 | T | A | 1 | a0007c0008t0006g0226 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.6502-512A>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47858024 | |||||||
chr3:47858076 | C | T | 1 | a0002c0002t0002g0066 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.6502-564G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47858076 | |||||||
chr3:47858388 | G | T | 33 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0134 others(30): Show |
33 | HG00544.hp1 HG00609.hp2 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.6502-876C>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47858388 | |||||||
chr3:47858586 | G | GGT | 9 | a0001c0001t0001g0128 a0001c0001t0001g0214 a0001c0001t0001g0216 others(6): Show |
9 | HG00544.hp1 NA18940.hp1 NA18982.hp1 others(6): Show |
intron_variant | MODIFIER | c.6502-1076_6502-107 others(6): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47858586 | |||||||
chr3:47858586 | G | GGTGT | 37 | a0002c0002t0002g0001 a0002c0002t0002g0052 a0002c0002t0002g0055 others(34): Show |
38 | HG00280.hp2 HG00639.hp1 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.6502-1078_6502-107 others(8): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47858586 | |||||||
chr3:47858586 | G | GGTGTGT | 13 | a0002c0002t0002g0082 a0002c0002t0002g0093 a0002c0002t0013g0065 others(10): Show |
13 | HG00733.hp1 HG00738.hp1 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.6502-1080_6502-107 others(10): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47858586 | |||||||
chr3:47858586 | G | GGTGTGTG others(1): Show |
5 | a0003c0003t0003g0098 a0003c0003t0003g0099 a0005c0005t0003g0119 others(2): Show |
5 | HG02630.hp1 HG02723.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.6502-1082_6502-107 others(12): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47858586 | |||||||
chr3:47858586 | G | GGTGTGTG others(3): Show |
14 | a0003c0003t0003g0095 a0003c0003t0003g0100 a0003c0003t0003g0101 others(11): Show |
14 | HG01109.hp2 HG02055.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.6502-1084_6502-107 others(14): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47858586 | |||||||
chr3:47858586 | G | GGTGTGTG others(5): Show |
5 | a0004c0004t0011g0049 a0004c0004t0011g0050 a0011c0015t0003g0096 others(2): Show |
5 | HG02717.hp2 HG02886.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.6502-1086_6502-107 others(16): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47858586 | |||||||
chr3:47858586 | G | GGTGTGTG others(7): Show |
1 | a0009c0009t0002g0047 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.6502-1088_6502-107 others(18): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47858586 | |||||||
chr3:47858586 | GGT | G | 4 | a0001c0001t0001g0132 a0001c0001t0001g0190 a0001c0001t0001g0227 others(1): Show |
4 | HG02083.hp1 HG02559.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.6502-1076_6502-107 others(6): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47858586 | |||||||
chr3:47858614 | T | C | 5 | a0004c0004t0002g0083 a0007c0008t0006g0149 a0007c0008t0006g0152 others(2): Show |
5 | HG01891.hp1 HG02083.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.6502-1102A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47858614 | |||||||
chr3:47858614 | T | TGTGC | 4 | a0002c0002t0002g0027 a0002c0002t0002g0029 a0002c0002t0002g0032 others(1): Show |
4 | HG00544.hp2 HG02735.hp1 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.6502-1103_6502-110 others(8): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47858614 | |||||||
chr3:47858616 | C | T | 11 | a0001c0001t0001g0141 a0002c0002t0002g0045 a0002c0002t0002g0056 others(8): Show |
11 | HG01255.hp1 HG02559.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.6502-1104G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47858616 | |||||||
chr3:47858620 | T | C | 22 | a0002c0002t0002g0030 a0002c0002t0002g0034 a0002c0002t0002g0035 others(19): Show |
22 | HG01884.hp1 HG02040.hp2 HG02071.hp2 others(19): Show |
intron_variant | MODIFIER | c.6502-1108A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47858620 | |||||||
chr3:47858620 | T | TTG | 6 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0009c0009t0002g0046 others(3): Show |
6 | HG00735.hp2 HG01109.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.6502-1110_6502-110 others(6): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47858620 | |||||||
chr3:47858620 | TTG | T | 92 | a0002c0002t0002g0001 a0002c0002t0002g0004 a0002c0002t0002g0005 others(89): Show |
93 | HG00099.hp2 HG00280.hp2 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.6502-1110_6502-110 others(6): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47858620 | |||||||
chr3:47858621 | T | G | 23 | a0002c0002t0002g0030 a0002c0002t0002g0034 a0002c0002t0002g0035 others(20): Show |
23 | HG01884.hp1 HG02040.hp2 HG02071.hp2 others(20): Show |
intron_variant | MODIFIER | c.6502-1109A>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47858621 | |||||||
chr3:47858622 | G | T | 23 | a0002c0002t0002g0030 a0002c0002t0002g0034 a0002c0002t0002g0035 others(20): Show |
23 | HG01884.hp1 HG02040.hp2 HG02071.hp2 others(20): Show |
intron_variant | MODIFIER | c.6502-1110C>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47858622 | |||||||
chr3:47858895 | A | G | 1 | a0002c0002t0002g0063 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.6502-1383T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47858895 | |||||||
chr3:47859213 | C | T | 124 | a0002c0002t0002g0001 a0002c0002t0002g0004 a0002c0002t0002g0005 others(121): Show |
125 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.6502-1701G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47859213 | |||||||
chr3:47859444 | G | A | 3 | a0001c0001t0001g0127 a0001c0001t0001g0136 a0001c0001t0016g0135 |
3 | HG03139.hp1 NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.6502-1932C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47859444 | |||||||
chr3:47859649 | A | G | 1 | a0004c0004t0011g0049 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.6502-2137T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47859649 | |||||||
chr3:47859897 | C | T | 1 | a0001c0001t0001g0198 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.6502-2385G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47859897 | |||||||
chr3:47859989 | A | C | 1 | a0004c0004t0002g0084 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.6502-2477T>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47859989 | |||||||
chr3:47860255 | G | A | 1 | a0001c0001t0001g0211 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.6502-2743C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47860255 | |||||||
chr3:47860313 | C | A | 89 | a0002c0002t0002g0001 a0002c0002t0002g0027 a0002c0002t0002g0029 others(86): Show |
90 | HG00280.hp2 HG00544.hp2 HG00639.hp1 others(87): Show |
intron_variant | MODIFIER | c.6502-2801G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47860313 | |||||||
chr3:47860757 | C | T | 8 | a0002c0002t0002g0045 a0002c0002t0002g0055 a0002c0002t0002g0056 others(5): Show |
8 | HG02559.hp1 HG02572.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.6502-3245G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47860757 | |||||||
chr3:47860994 | C | T | 1 | a0021c0028t0002g0224 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.6502-3482G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47860994 | |||||||
chr3:47861153 | G | T | 1 | a0001c0001t0001g0134 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.6502-3641C>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47861153 | |||||||
chr3:47861353 | C | CT | 85 | a0001c0001t0001g0144 a0001c0001t0001g0158 a0001c0001t0001g0189 others(82): Show |
86 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.6502-3842dupA | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47861353 | |||||||
chr3:47861353 | C | CTT | 9 | a0003c0003t0003g0107 a0004c0004t0002g0085 a0004c0004t0020g0080 others(6): Show |
9 | HG01123.hp2 HG01884.hp1 HG01934.hp1 others(6): Show |
intron_variant | MODIFIER | c.6502-3843_6502-384 others(6): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47861353 | |||||||
chr3:47861470 | A | T | 1 | a0004c0004t0018g0060 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.6502-3958T>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47861470 | |||||||
chr3:47861693 | G | C | 2 | a0001c0001t0001g0128 a0009c0009t0002g0047 |
2 | HG01891.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.6502-4181C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47861693 | |||||||
chr3:47861764 | C | A | 1 | a0002c0002t0002g0036 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.6502-4252G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47861764 | |||||||
chr3:47861815 | C | T | 49 | a0002c0002t0002g0001 a0002c0002t0002g0027 a0002c0002t0002g0029 others(46): Show |
50 | HG00280.hp2 HG00544.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.6502-4303G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47861815 | |||||||
chr3:47861934 | G | A | 49 | a0002c0002t0002g0001 a0002c0002t0002g0027 a0002c0002t0002g0029 others(46): Show |
50 | HG00280.hp2 HG00544.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.6502-4422C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47861934 | |||||||
chr3:47862029 | C | T | 1 | a0004c0004t0017g0086 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.6502-4517G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47862029 | |||||||
chr3:47862161 | C | CA | 15 | a0001c0001t0001g0041 a0001c0001t0001g0126 a0001c0001t0001g0141 others(12): Show |
15 | HG00609.hp1 HG01109.hp1 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.6502-4650dupT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47862161 | |||||||
chr3:47862161 | CA | C | 35 | a0001c0001t0001g0211 a0002c0002t0002g0005 a0002c0002t0002g0010 others(32): Show |
35 | HG00099.hp2 HG00673.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.6502-4650delT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47862161 | |||||||
chr3:47862161 | CAA | C | 80 | a0002c0002t0002g0001 a0002c0002t0002g0027 a0002c0002t0002g0029 others(77): Show |
81 | HG00280.hp2 HG00544.hp2 HG00639.hp1 others(78): Show |
intron_variant | MODIFIER | c.6502-4651_6502-465 others(6): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47862161 | |||||||
chr3:47862346 | C | CA | 23 | a0001c0001t0001g0147 a0001c0001t0001g0163 a0001c0001t0001g0170 others(20): Show |
23 | HG00544.hp1 HG00609.hp2 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.6502-4835dupT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47862346 | |||||||
chr3:47862346 | C | CAA | 5 | a0001c0001t0001g0156 a0001c0001t0001g0173 a0001c0001t0001g0177 others(2): Show |
5 | HG01891.hp1 HG02071.hp1 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.6502-4836_6502-483 others(6): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47862346 | |||||||
chr3:47862346 | CA | C | 30 | a0001c0001t0001g0043 a0001c0001t0001g0138 a0001c0001t0001g0139 others(27): Show |
31 | HG00280.hp1 HG00280.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.6502-4835delT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47862346 | |||||||
chr3:47862346 | CAA | C | 12 | a0002c0002t0002g0090 a0003c0003t0003g0102 a0004c0004t0002g0083 others(9): Show |
12 | HG01934.hp1 HG02040.hp2 HG02071.hp2 others(9): Show |
intron_variant | MODIFIER | c.6502-4836_6502-483 others(6): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47862346 | |||||||
chr3:47862346 | CAAA | C | 27 | a0002c0002t0002g0027 a0002c0002t0002g0029 a0002c0002t0002g0030 others(24): Show |
27 | HG00544.hp2 HG00738.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.6502-4837_6502-483 others(7): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47862346 | |||||||
chr3:47862346 | CAAAA | C | 9 | a0005c0005t0003g0114 a0005c0005t0003g0115 a0005c0005t0003g0116 others(6): Show |
9 | HG01884.hp1 HG01891.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.6502-4838_6502-483 others(8): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47862346 | |||||||
chr3:47862346 | CAAAAAAA | C | 14 | a0002c0002t0002g0045 a0002c0002t0002g0055 a0002c0002t0002g0056 others(11): Show |
14 | HG01123.hp2 HG02451.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.6502-4841_6502-483 others(11): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47862346 | |||||||
chr3:47862346 | CAAAAAAA others(2): Show |
C | 10 | a0002c0002t0002g0020 a0002c0002t0002g0036 a0002c0002t0002g0037 others(7): Show |
10 | HG01074.hp2 HG01346.hp2 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.6502-4843_6502-483 others(13): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47862346 | |||||||
chr3:47862346 | CAAAAAAA others(3): Show |
C | 24 | a0002c0002t0002g0004 a0002c0002t0002g0005 a0002c0002t0002g0010 others(21): Show |
24 | HG00099.hp2 HG00597.hp2 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.6502-4844_6502-483 others(14): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47862346 | |||||||
chr3:47862445 | T | C | 1 | a0001c0001t0001g0229 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.6501+4801A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47862445 | |||||||
chr3:47863063 | G | A | 4 | a0002c0002t0002g0021 a0002c0002t0002g0024 a0002c0002t0002g0025 others(1): Show |
4 | HG00099.hp2 HG01496.hp2 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.6501+4183C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47863063 | |||||||
chr3:47863454 | C | T | 3 | a0010c0013t0010g0002 a0010c0013t0010g0222 a0021c0028t0002g0224 |
3 | HG02145.hp2 HG02451.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.6501+3792G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47863454 | |||||||
chr3:47863589 | G | A | 49 | a0002c0002t0002g0001 a0002c0002t0002g0027 a0002c0002t0002g0029 others(46): Show |
50 | HG00280.hp2 HG00544.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.6501+3657C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47863589 | |||||||
chr3:47863674 | T | A | 1 | a0004c0004t0018g0060 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.6501+3572A>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47863674 | |||||||
chr3:47863921 | G | GGGGTGTG others(7): Show |
1 | a0022c0030t0023g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.6501+3324_6501+332 others(18): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47863921 | |||||||
chr3:47863921 | G | GGTGTGTG others(7): Show |
31 | a0002c0002t0002g0004 a0002c0002t0002g0005 a0002c0002t0002g0010 others(28): Show |
31 | HG00099.hp2 HG00597.hp2 HG00673.hp2 others(28): Show |
intron_variant | MODIFIER | c.6501+3311_6501+332 others(18): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47863921 | |||||||
chr3:47863921 | G | GGTGTGTG others(9): Show |
1 | a0002c0002t0002g0020 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.6501+3309_6501+332 others(20): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47863921 | |||||||
chr3:47863921 | G | GGTGTGTG others(13): Show |
1 | a0010c0013t0010g0002 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.6501+3324_6501+332 others(24): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47863921 | |||||||
chr3:47863921 | G | GGTGTGTG others(31): Show |
1 | a0021c0028t0002g0224 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.6501+3324_6501+332 others(42): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47863921 | |||||||
chr3:47863921 | G | T | 1 | a0004c0004t0002g0083 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.6501+3325C>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47863921 | |||||||
chr3:47863923 | T | G | 1 | a0001c0001t0001g0208 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.6501+3323A>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47863923 | |||||||
chr3:47863937 | T | TGTGGGGG others(6): Show |
2 | a0002c0002t0002g0052 a0002c0002t0002g0072 |
2 | HG02015.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.6501+3308_6501+330 others(17): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47863937 | |||||||
chr3:47863937 | T | TGTGTGGG others(3): Show |
1 | a0009c0009t0002g0046 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.6501+3308_6501+330 others(14): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47863937 | |||||||
chr3:47863937 | T | TGTGTGGG others(4): Show |
1 | a0027c0032t0002g0059 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.6501+3308_6501+330 others(15): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47863937 | |||||||
chr3:47863937 | T | TGTGTGGG others(5): Show |
11 | a0002c0002t0002g0027 a0002c0002t0002g0032 a0002c0002t0002g0033 others(8): Show |
11 | HG02559.hp1 HG02735.hp1 HG02976.hp2 others(8): Show |
intron_variant | MODIFIER | c.6501+3308_6501+330 others(16): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47863937 | |||||||
chr3:47863937 | T | TGTGTGGG others(6): Show |
2 | a0002c0002t0002g0029 a0002c0002t0002g0030 |
2 | HG00544.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.6501+3308_6501+330 others(17): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47863937 | |||||||
chr3:47863937 | T | TGTGTGGG others(7): Show |
1 | a0026c0019t0002g0077 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.6501+3308_6501+330 others(18): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47863937 | |||||||
chr3:47863937 | T | TGTGTGTG others(3): Show |
3 | a0003c0003t0003g0102 a0009c0009t0002g0047 a0009c0009t0002g0048 |
3 | HG01891.hp2 HG02258.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.6501+3308_6501+330 others(14): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47863937 | |||||||
chr3:47863937 | T | TGTGTGTG others(5): Show |
28 | a0002c0002t0002g0001 a0002c0002t0002g0045 a0002c0002t0002g0051 others(25): Show |
29 | HG00280.hp2 HG00639.hp1 HG00733.hp1 others(26): Show |
intron_variant | MODIFIER | c.6501+3308_6501+330 others(16): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47863937 | |||||||
chr3:47863937 | T | TGTGTGTG others(6): Show |
2 | a0002c0002t0002g0066 a0002c0002t0002g0068 |
2 | HG01099.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.6501+3308_6501+330 others(17): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47863937 | |||||||
chr3:47863937 | T | TGTGTGTG others(7): Show |
1 | a0004c0004t0020g0080 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.6501+3308_6501+330 others(18): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47863937 | |||||||
chr3:47863937 | T | TGTGTGTG others(35): Show |
1 | a0010c0013t0010g0222 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.6501+3308_6501+330 others(46): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47863937 | |||||||
chr3:47863937 | T | TGTGTGTG others(3): Show |
24 | a0003c0003t0003g0095 a0003c0003t0003g0098 a0003c0003t0003g0099 others(21): Show |
24 | HG00738.hp1 HG01109.hp2 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.6501+3308_6501+330 others(14): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47863937 | |||||||
chr3:47863937 | T | TGTGTGTG others(5): Show |
2 | a0002c0002t0002g0231 a0004c0004t0017g0086 |
2 | HG00741.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.6501+3308_6501+330 others(16): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47863937 | |||||||
chr3:47863937 | T | TGTGTGTG others(7): Show |
1 | a0004c0004t0011g0050 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.6501+3308_6501+330 others(18): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47863937 | |||||||
chr3:47863937 | T | TGTGTGTG others(5): Show |
1 | a0003c0003t0003g0103 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.6501+3308_6501+330 others(16): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47863937 | |||||||
chr3:47863937 | T | TGTGTGTG others(7): Show |
7 | a0004c0004t0002g0083 a0004c0004t0002g0084 a0004c0004t0002g0085 others(4): Show |
7 | HG02040.hp2 HG02071.hp2 HG02083.hp2 others(4): Show |
intron_variant | MODIFIER | c.6501+3308_6501+330 others(18): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47863937 | |||||||
chr3:47864046 | C | T | 10 | a0004c0004t0002g0083 a0004c0004t0002g0084 a0004c0004t0002g0085 others(7): Show |
10 | HG01934.hp1 HG02040.hp2 HG02071.hp2 others(7): Show |
intron_variant | MODIFIER | c.6501+3200G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47864046 | |||||||
chr3:47864080 | G | C | 124 | a0002c0002t0002g0001 a0002c0002t0002g0004 a0002c0002t0002g0005 others(121): Show |
125 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.6501+3166C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47864080 | |||||||
chr3:47864414 | T | C | 4 | a0002c0002t0002g0123 a0002c0011t0002g0073 a0002c0011t0002g0087 others(1): Show |
4 | HG00639.hp1 HG00733.hp1 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.6501+2832A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47864414 | |||||||
chr3:47864451 | C | T | 1 | a0002c0002t0005g0028 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.6501+2795G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47864451 | |||||||
chr3:47864521 | T | TA | 3 | a0001c0007t0001g0218 a0007c0008t0006g0131 a0007c0008t0006g0226 |
3 | HG03540.hp2 NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.6501+2724dupT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47864521 | |||||||
chr3:47864577 | T | C | 1 | a0001c0001t0001g0162 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.6501+2669A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47864577 | |||||||
chr3:47864614 | T | C | 6 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(3): Show |
6 | HG01255.hp1 HG02015.hp1 NA18941.hp2 others(3): Show |
intron_variant | MODIFIER | c.6501+2632A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47864614 | |||||||
chr3:47864620 | T | C | 1 | a0001c0001t0001g0179 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.6501+2626A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47864620 | |||||||
chr3:47864693 | C | A | 1 | a0001c0001t0001g0157 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.6501+2553G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47864693 | |||||||
chr3:47864781 | C | T | 1 | a0002c0002t0002g0082 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.6501+2465G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47864781 | |||||||
chr3:47864818 | G | A | 1 | a0010c0013t0010g0002 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.6501+2428C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47864818 | |||||||
chr3:47864845 | C | T | 1 | a0023c0022t0002g0088 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.6501+2401G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47864845 | |||||||
chr3:47865135 | CAAAA | C | 3 | a0010c0013t0010g0002 a0010c0013t0010g0222 a0021c0028t0002g0224 |
3 | HG02145.hp2 HG02451.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.6501+2107_6501+211 others(8): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47865135 | |||||||
chr3:47865516 | G | GGA | 124 | a0002c0002t0002g0001 a0002c0002t0002g0004 a0002c0002t0002g0005 others(121): Show |
125 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.6501+1728_6501+172 others(6): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47865516 | |||||||
chr3:47865856 | G | A | 4 | a0001c0001t0001g0126 a0001c0001t0001g0200 a0001c0001t0001g0201 others(1): Show |
4 | HG00609.hp1 HG00673.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.6501+1390C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47865856 | |||||||
chr3:47866168 | C | T | 1 | a0002c0002t0002g0066 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.6501+1078G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47866168 | |||||||
chr3:47866229 | T | C | 125 | a0001c0001t0001g0183 a0002c0002t0002g0001 a0002c0002t0002g0004 others(122): Show |
126 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.6501+1017A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47866229 | |||||||
chr3:47866347 | A | AAAAC | 4 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0177 others(1): Show |
4 | HG02922.hp2 NA18946.hp2 NA18956.hp2 others(1): Show |
intron_variant | MODIFIER | c.6501+895_6501+898d others(6): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47866347 | |||||||
chr3:47866347 | AAAAC | A | 4 | a0001c0001t0009g0178 a0002c0002t0013g0065 a0004c0004t0011g0049 others(1): Show |
4 | HG03041.hp2 HG03453.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.6501+895_6501+898d others(6): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47866347 | |||||||
chr3:47866359 | C | G | 1 | a0003c0003t0003g0099 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.6501+887G>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47866359 | |||||||
chr3:47866474 | G | A | 1 | a0001c0001t0009g0178 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.6501+772C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47866474 | |||||||
chr3:47866639 | G | A | 17 | a0003c0003t0003g0095 a0003c0003t0003g0098 a0003c0003t0003g0099 others(14): Show |
17 | HG01109.hp2 HG02055.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.6501+607C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47866639 | |||||||
chr3:47867192 | A | G | 1 | a0002c0002t0002g0036 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.6501+54T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 17/20 | chr3 | 47867192 | |||||||
chr3:47867571 | C | T | 1 | a0002c0002t0004g0015 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.6409-233G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 16/20 | chr3 | 47867571 | |||||||
chr3:47867591 | C | T | 1 | a0004c0004t0018g0060 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.6409-253G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 16/20 | chr3 | 47867591 | |||||||
chr3:47867703 | C | G | 2 | a0004c0004t0011g0049 a0004c0004t0011g0050 |
2 | HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.6409-365G>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 16/20 | chr3 | 47867703 | |||||||
chr3:47867890 | G | C | 5 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(2): Show |
5 | HG01074.hp1 HG01169.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.6409-552C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 16/20 | chr3 | 47867890 | |||||||
chr3:47868365 | A | T | 1 | a0002c0002t0002g0051 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.6408+849T>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 16/20 | chr3 | 47868365 | |||||||
chr3:47868547 | C | T | 1 | a0016c0027t0001g0175 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.6408+667G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 16/20 | chr3 | 47868547 | |||||||
chr3:47868598 | C | T | 1 | a0010c0013t0010g0002 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.6408+616G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 16/20 | chr3 | 47868598 | |||||||
chr3:47869540 | A | C | 1 | a0002c0002t0002g0120 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.6295-213T>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 15/20 | chr3 | 47869540 | |||||||
chr3:47869631 | G | A | 3 | a0002c0002t0002g0001 a0002c0002t0002g0061 a0002c0002t0002g0068 |
4 | HG01099.hp1 HG01169.hp2 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.6295-304C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 15/20 | chr3 | 47869631 | |||||||
chr3:47869701 | A | G | 1 | a0010c0013t0010g0222 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.6295-374T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 15/20 | chr3 | 47869701 | |||||||
chr3:47869701 | A | T | 1 | a0002c0002t0002g0120 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.6295-374T>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 15/20 | chr3 | 47869701 | |||||||
chr3:47869784 | A | C | 1 | a0005c0005t0003g0117 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.6295-457T>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 15/20 | chr3 | 47869784 | |||||||
chr3:47869830 | C | G | 4 | a0002c0002t0005g0026 a0002c0002t0005g0028 a0002c0002t0005g0040 others(1): Show |
4 | HG01074.hp2 HG01346.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.6295-503G>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 15/20 | chr3 | 47869830 | |||||||
chr3:47870031 | C | T | 38 | a0002c0002t0002g0004 a0002c0002t0002g0005 a0002c0002t0002g0010 others(35): Show |
38 | HG00099.hp2 HG00544.hp2 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.6295-704G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 15/20 | chr3 | 47870031 | |||||||
chr3:47870157 | C | G | 1 | a0001c0001t0001g0186 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.6294+656G>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 15/20 | chr3 | 47870157 | |||||||
chr3:47870237 | C | T | 31 | a0002c0002t0002g0004 a0002c0002t0002g0005 a0002c0002t0002g0010 others(28): Show |
31 | HG00099.hp2 HG00597.hp2 HG00673.hp2 others(28): Show |
intron_variant | MODIFIER | c.6294+576G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 15/20 | chr3 | 47870237 | |||||||
chr3:47870268 | T | C | 2 | a0007c0008t0006g0131 a0007c0008t0006g0226 |
2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.6294+545A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 15/20 | chr3 | 47870268 | |||||||
chr3:47871536 | A | AGCCCTCT others(31): Show |
1 | a0002c0002t0002g0057 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.5942-288_5942-251d others(40): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 13/20 | chr3 | 47871536 | |||||||
chr3:47872636 | C | A | 1 | a0007c0008t0006g0226 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.5758-536G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 12/20 | chr3 | 47872636 | |||||||
chr3:47872796 | C | G | 1 | a0021c0028t0002g0224 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.5758-696G>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 12/20 | chr3 | 47872796 | |||||||
chr3:47872972 | T | G | 1 | a0005c0005t0003g0116 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.5758-872A>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 12/20 | chr3 | 47872972 | |||||||
chr3:47872986 | G | A | 3 | a0010c0013t0010g0002 a0010c0013t0010g0222 a0021c0028t0002g0224 |
3 | HG02145.hp2 HG02451.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.5758-886C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 12/20 | chr3 | 47872986 | |||||||
chr3:47873287 | G | A | 4 | a0002c0002t0005g0026 a0002c0002t0005g0028 a0002c0002t0005g0040 others(1): Show |
4 | HG01074.hp2 HG01346.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.5758-1187C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 12/20 | chr3 | 47873287 | |||||||
chr3:47873339 | G | A | 29 | a0003c0003t0003g0095 a0003c0003t0003g0098 a0003c0003t0003g0099 others(26): Show |
29 | HG00738.hp1 HG01109.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.5758-1239C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 12/20 | chr3 | 47873339 | |||||||
chr3:47873484 | C | T | 4 | a0001c0001t0001g0208 a0001c0001t0001g0210 a0001c0001t0001g0211 others(1): Show |
4 | HG01257.hp2 HG01258.hp1 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.5758-1384G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 12/20 | chr3 | 47873484 | |||||||
chr3:47873541 | T | G | 3 | a0008c0010t0007g0111 a0008c0010t0007g0112 a0008c0010t0007g0113 |
3 | HG00738.hp1 HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.5758-1441A>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 12/20 | chr3 | 47873541 | |||||||
chr3:47873592 | A | T | 2 | a0002c0002t0002g0045 a0002c0002t0002g0055 |
2 | HG03098.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.5758-1492T>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 12/20 | chr3 | 47873592 | |||||||
chr3:47873628 | A | G | 124 | a0002c0002t0002g0001 a0002c0002t0002g0004 a0002c0002t0002g0005 others(121): Show |
125 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.5758-1528T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 12/20 | chr3 | 47873628 | |||||||
chr3:47874215 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.5757+1470G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 12/20 | chr3 | 47874215 | |||||||
chr3:47874293 | C | T | 1 | a0002c0002t0002g0123 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.5757+1392G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 12/20 | chr3 | 47874293 | |||||||
chr3:47874450 | C | G | 1 | a0023c0022t0002g0088 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.5757+1235G>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 12/20 | chr3 | 47874450 | |||||||
chr3:47874909 | A | G | 1 | a0002c0002t0002g0033 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.5757+776T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 12/20 | chr3 | 47874909 | |||||||
chr3:47875002 | T | C | 1 | a0001c0001t0001g0229 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.5757+683A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 12/20 | chr3 | 47875002 | |||||||
chr3:47875658 | C | T | 1 | a0002c0002t0002g0039 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.5757+27G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 12/20 | chr3 | 47875658 | |||||||
chr3:47876132 | C | CT | 3 | a0001c0001t0001g0211 a0001c0001t0001g0229 a0001c0007t0001g0219 |
3 | HG01257.hp2 HG02572.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.5542-233dupA | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 11/20 | chr3 | 47876132 | |||||||
chr3:47876132 | CTTTCTT | C | 119 | a0002c0002t0002g0001 a0002c0002t0002g0004 a0002c0002t0002g0005 others(116): Show |
120 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(117): Show |
intron_variant | MODIFIER | c.5542-238_5542-233d others(8): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 11/20 | chr3 | 47876132 | |||||||
chr3:47876136 | C | T | 51 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(48): Show |
51 | HG00544.hp1 HG00609.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.5542-236G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 11/20 | chr3 | 47876136 | |||||||
chr3:47876244 | G | C | 1 | a0001c0001t0001g0161 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.5542-344C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 11/20 | chr3 | 47876244 | |||||||
chr3:47876282 | C | A | 1 | a0022c0030t0023g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.5542-382G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 11/20 | chr3 | 47876282 | |||||||
chr3:47876557 | CAGG | C | 29 | a0003c0003t0003g0095 a0003c0003t0003g0098 a0003c0003t0003g0099 others(26): Show |
29 | HG00738.hp1 HG01109.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.5542-660_5542-658d others(5): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 11/20 | chr3 | 47876557 | |||||||
chr3:47876885 | G | T | 1 | a0001c0001t0001g0193 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.5541+532C>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 11/20 | chr3 | 47876885 | |||||||
chr3:47876903 | C | CT | 9 | a0001c0001t0001g0126 a0001c0001t0001g0134 a0001c0001t0001g0200 others(6): Show |
9 | HG00609.hp1 HG00639.hp2 HG00673.hp1 others(6): Show |
intron_variant | MODIFIER | c.5541+513dupA | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 11/20 | chr3 | 47876903 | |||||||
chr3:47877793 | T | C | 1 | a0001c0001t0001g0189 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.5435-270A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47877793 | |||||||
chr3:47877846 | T | C | 1 | a0001c0001t0001g0189 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.5435-323A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47877846 | |||||||
chr3:47878139 | T | C | 1 | a0002c0002t0002g0082 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.5435-616A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47878139 | |||||||
chr3:47878227 | G | A | 3 | a0002c0002t0005g0028 a0002c0002t0005g0040 a0018c0016t0005g0031 |
3 | HG01074.hp2 HG01346.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.5435-704C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47878227 | |||||||
chr3:47878750 | C | T | 80 | a0002c0002t0002g0001 a0002c0002t0002g0004 a0002c0002t0002g0005 others(77): Show |
81 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.5435-1227G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47878750 | |||||||
chr3:47878847 | A | ATT | 124 | a0002c0002t0002g0001 a0002c0002t0002g0004 a0002c0002t0002g0005 others(121): Show |
125 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.5435-1326_5435-132 others(6): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47878847 | |||||||
chr3:47879240 | GA | G | 15 | a0003c0003t0003g0095 a0003c0003t0003g0098 a0003c0003t0003g0099 others(12): Show |
15 | HG01109.hp2 HG02055.hp2 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.5435-1718delT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47879240 | |||||||
chr3:47879318 | T | C | 1 | a0010c0013t0010g0002 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.5435-1795A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47879318 | |||||||
chr3:47879675 | AACC | A | 79 | a0002c0002t0002g0001 a0002c0002t0002g0004 a0002c0002t0002g0005 others(76): Show |
80 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.5435-2155_5435-215 others(7): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47879675 | |||||||
chr3:47879752 | T | C | 2 | a0001c0001t0001g0214 a0001c0001t0001g0216 |
2 | NA18982.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.5435-2229A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47879752 | |||||||
chr3:47879903 | G | A | 1 | a0010c0013t0010g0002 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.5435-2380C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47879903 | |||||||
chr3:47880021 | TGA | T | 3 | a0009c0009t0002g0046 a0009c0009t0002g0047 a0009c0009t0002g0048 |
3 | HG01891.hp2 HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.5435-2500_5435-249 others(6): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47880021 | |||||||
chr3:47880061 | G | A | 1 | a0002c0002t0002g0089 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.5435-2538C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47880061 | |||||||
chr3:47880180 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.5435-2657G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47880180 | |||||||
chr3:47880214 | C | T | 38 | a0002c0002t0002g0004 a0002c0002t0002g0005 a0002c0002t0002g0010 others(35): Show |
38 | HG00099.hp2 HG00544.hp2 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.5435-2691G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47880214 | |||||||
chr3:47880251 | C | G | 1 | a0001c0001t0001g0171 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.5435-2728G>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47880251 | |||||||
chr3:47880259 | A | AT | 17 | a0001c0001t0001g0129 a0001c0001t0001g0139 a0001c0001t0001g0153 others(14): Show |
17 | HG00741.hp1 HG01981.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.5435-2737dupA | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47880259 | |||||||
chr3:47880259 | AT | A | 77 | a0001c0001t0001g0147 a0001c0001t0001g0156 a0001c0001t0001g0159 others(74): Show |
77 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.5435-2737delA | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47880259 | |||||||
chr3:47880259 | ATT | A | 6 | a0004c0004t0002g0083 a0004c0004t0002g0084 a0004c0004t0002g0085 others(3): Show |
6 | HG02040.hp2 HG02071.hp2 HG02083.hp2 others(3): Show |
intron_variant | MODIFIER | c.5435-2738_5435-273 others(6): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47880259 | |||||||
chr3:47880302 | G | A | 2 | a0002c0002t0002g0069 a0002c0002t0002g0231 |
2 | HG00741.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.5435-2779C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47880302 | |||||||
chr3:47880343 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.5435-2820G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47880343 | |||||||
chr3:47880359 | C | T | 1 | a0004c0004t0017g0086 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.5435-2836G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47880359 | |||||||
chr3:47880393 | C | A | 2 | a0012c0012t0002g0071 a0012c0012t0002g0078 |
2 | HG04115.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.5435-2870G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47880393 | |||||||
chr3:47880465 | G | GT | 15 | a0001c0001t0001g0151 a0001c0001t0001g0157 a0001c0001t0001g0160 others(12): Show |
15 | HG00544.hp1 HG00741.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.5435-2943dupA | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47880465 | |||||||
chr3:47880465 | G | GTT | 90 | a0002c0002t0002g0001 a0002c0002t0002g0004 a0002c0002t0002g0010 others(87): Show |
91 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.5435-2944_5435-294 others(6): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47880465 | |||||||
chr3:47880465 | G | GTTT | 16 | a0002c0002t0002g0005 a0002c0002t0002g0012 a0002c0002t0002g0024 others(13): Show |
16 | HG00597.hp2 HG00735.hp1 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.5435-2945_5435-294 others(7): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47880465 | |||||||
chr3:47880465 | GT | G | 5 | a0001c0001t0001g0146 a0001c0001t0001g0171 a0001c0001t0001g0186 others(2): Show |
5 | HG01099.hp2 HG02451.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.5435-2943delA | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47880465 | |||||||
chr3:47880508 | T | C | 2 | a0001c0001t0008g0166 a0001c0001t0008g0167 |
2 | HG02258.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.5435-2985A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47880508 | |||||||
chr3:47880673 | A | C | 1 | a0002c0002t0002g0018 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.5435-3150T>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47880673 | |||||||
chr3:47880690 | C | T | 2 | a0002c0002t0002g0037 a0002c0002t0002g0039 |
2 | HG02135.hp1 NA18946.hp1 |
intron_variant | MODIFIER | c.5435-3167G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47880690 | |||||||
chr3:47880753 | A | ATGCCCCA others(17): Show |
1 | a0002c0002t0002g0120 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.5435-3254_5435-323 others(28): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47880753 | |||||||
chr3:47881446 | C | CTA | 12 | a0001c0001t0001g0138 a0001c0001t0001g0144 a0001c0001t0001g0158 others(9): Show |
12 | HG01109.hp1 HG01516.hp2 HG02015.hp1 others(9): Show |
intron_variant | MODIFIER | c.5435-3925_5435-392 others(6): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47881446 | |||||||
chr3:47881446 | C | CTACATAT others(5): Show |
1 | a0001c0001t0001g0147 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.5435-3924_5435-392 others(16): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47881446 | |||||||
chr3:47881446 | C | CTATA | 19 | a0001c0001t0001g0067 a0001c0001t0001g0126 a0001c0001t0001g0141 others(16): Show |
19 | HG00544.hp1 HG00609.hp1 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.5435-3927_5435-392 others(8): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47881446 | |||||||
chr3:47881446 | C | CTATATA | 18 | a0001c0001t0001g0128 a0001c0001t0001g0132 a0001c0001t0001g0136 others(15): Show |
18 | HG00735.hp2 HG01123.hp1 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.5435-3929_5435-392 others(10): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47881446 | |||||||
chr3:47881446 | C | CTATATAT others(1): Show |
13 | a0001c0001t0001g0139 a0001c0001t0001g0160 a0001c0001t0001g0171 others(10): Show |
13 | HG00609.hp2 HG00741.hp1 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.5435-3931_5435-392 others(12): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47881446 | |||||||
chr3:47881446 | C | CTATATAT others(3): Show |
9 | a0001c0001t0001g0042 a0001c0001t0001g0140 a0001c0001t0001g0164 others(6): Show |
9 | HG01943.hp2 HG02148.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.5435-3933_5435-392 others(14): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47881446 | |||||||
chr3:47881446 | C | CTATATAT others(5): Show |
5 | a0001c0001t0001g0134 a0003c0003t0003g0099 a0008c0010t0007g0113 others(2): Show |
5 | HG00639.hp2 HG00738.hp1 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.5435-3935_5435-392 others(16): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47881446 | |||||||
chr3:47881446 | C | CTATATAT others(7): Show |
2 | a0001c0001t0001g0199 a0001c0001t0001g0225 |
2 | HG01884.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.5435-3937_5435-392 others(18): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47881446 | |||||||
chr3:47881446 | C | CTATATAT others(9): Show |
1 | a0001c0001t0001g0189 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.5435-3939_5435-392 others(20): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47881446 | |||||||
chr3:47881446 | C | CTATATAT others(17): Show |
2 | a0001c0001t0001g0157 a0001c0001t0024g0165 |
2 | HG03516.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.5435-3947_5435-392 others(28): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47881446 | |||||||
chr3:47881446 | CTA | C | 6 | a0001c0001t0001g0127 a0001c0001t0001g0196 a0001c0001t0001g0210 others(3): Show |
6 | HG01934.hp2 HG02055.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.5435-3925_5435-392 others(6): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47881446 | |||||||
chr3:47881446 | CTATA | C | 12 | a0001c0001t0001g0146 a0001c0001t0001g0161 a0001c0001t0001g0169 others(9): Show |
12 | HG00099.hp1 HG01099.hp2 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.5435-3927_5435-392 others(8): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47881446 | |||||||
chr3:47881446 | CTATATA | C | 4 | a0001c0001t0001g0195 a0001c0001t0001g0209 a0003c0003t0003g0100 others(1): Show |
4 | HG00738.hp2 HG03041.hp1 NA18953.hp2 others(1): Show |
intron_variant | MODIFIER | c.5435-3929_5435-392 others(10): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47881446 | |||||||
chr3:47881446 | CTATATAT others(1): Show |
C | 5 | a0001c0001t0001g0229 a0001c0007t0001g0218 a0001c0007t0001g0219 others(2): Show |
5 | HG02572.hp1 HG02735.hp2 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.5435-3931_5435-392 others(12): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47881446 | |||||||
chr3:47881446 | CTATATAT others(3): Show |
C | 7 | a0001c0001t0001g0186 a0001c0001t0001g0192 a0001c0001t0001g0206 others(4): Show |
7 | HG02486.hp1 HG02886.hp1 HG04204.hp2 others(4): Show |
intron_variant | MODIFIER | c.5435-3933_5435-392 others(14): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47881446 | |||||||
chr3:47881446 | CTATATAT others(5): Show |
C | 3 | a0001c0001t0001g0041 a0001c0001t0009g0205 a0005c0005t0003g0121 |
3 | HG02280.hp1 HG02723.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.5435-3935_5435-392 others(16): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47881446 | |||||||
chr3:47881446 | CTATATAT others(7): Show |
C | 1 | a0002c0002t0002g0057 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.5435-3937_5435-392 others(18): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47881446 | |||||||
chr3:47881446 | CTATATAT others(9): Show |
C | 13 | a0001c0001t0001g0151 a0001c0001t0001g0159 a0002c0002t0002g0045 others(10): Show |
13 | HG01891.hp2 HG02572.hp2 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.5435-3939_5435-392 others(20): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47881446 | |||||||
chr3:47881446 | CTATATAT others(11): Show |
C | 19 | a0001c0024t0001g0133 a0002c0002t0002g0051 a0002c0002t0002g0052 others(16): Show |
19 | HG00280.hp1 HG01981.hp2 HG02015.hp2 others(16): Show |
intron_variant | MODIFIER | c.5435-3941_5435-392 others(22): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47881446 | |||||||
chr3:47881446 | CTATATAT others(13): Show |
C | 17 | a0001c0001t0001g0043 a0002c0002t0002g0063 a0002c0002t0002g0068 others(14): Show |
17 | HG00280.hp2 HG00639.hp1 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.5435-3943_5435-392 others(24): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47881446 | |||||||
chr3:47881446 | CTATATAT others(15): Show |
C | 14 | a0002c0002t0002g0001 a0002c0002t0002g0061 a0002c0002t0002g0069 others(11): Show |
15 | HG00733.hp1 HG00741.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.5435-3945_5435-392 others(26): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47881446 | |||||||
chr3:47881446 | CTATATAT others(17): Show |
C | 37 | a0002c0002t0002g0004 a0002c0002t0002g0005 a0002c0002t0002g0010 others(34): Show |
37 | HG00099.hp2 HG00544.hp2 HG00597.hp2 others(34): Show |
intron_variant | MODIFIER | c.5435-3947_5435-392 others(28): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47881446 | |||||||
chr3:47881446 | CTATATAT others(19): Show |
C | 1 | a0010c0013t0010g0222 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.5435-3949_5435-392 others(30): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47881446 | |||||||
chr3:47881488 | A | G | 1 | a0001c0001t0002g0150 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.5435-3965T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47881488 | |||||||
chr3:47881489 | T | C | 1 | a0001c0001t0002g0150 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.5435-3966A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47881489 | |||||||
chr3:47881807 | G | T | 124 | a0002c0002t0002g0001 a0002c0002t0002g0004 a0002c0002t0002g0005 others(121): Show |
125 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.5435-4284C>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47881807 | |||||||
chr3:47881931 | T | C | 6 | a0004c0004t0002g0083 a0004c0004t0002g0084 a0004c0004t0002g0085 others(3): Show |
6 | HG02040.hp2 HG02071.hp2 HG02083.hp2 others(3): Show |
intron_variant | MODIFIER | c.5435-4408A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47881931 | |||||||
chr3:47882044 | C | T | 1 | a0001c0001t0001g0156 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.5435-4521G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47882044 | |||||||
chr3:47882136 | G | C | 1 | a0016c0027t0001g0175 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.5435-4613C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47882136 | |||||||
chr3:47882143 | G | A | 4 | a0001c0007t0001g0218 a0001c0007t0001g0219 a0001c0007t0001g0220 others(1): Show |
4 | HG02451.hp1 HG02572.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.5435-4620C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47882143 | |||||||
chr3:47882509 | T | TA | 29 | a0003c0003t0003g0095 a0003c0003t0003g0098 a0003c0003t0003g0099 others(26): Show |
29 | HG00738.hp1 HG01109.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.5435-4987dupT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47882509 | |||||||
chr3:47882726 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.5435-5203G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47882726 | |||||||
chr3:47882757 | G | C | 1 | a0022c0030t0023g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.5435-5234C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47882757 | |||||||
chr3:47882827 | G | C | 119 | a0002c0002t0002g0001 a0002c0002t0002g0004 a0002c0002t0002g0005 others(116): Show |
120 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(117): Show |
intron_variant | MODIFIER | c.5435-5304C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47882827 | |||||||
chr3:47882895 | C | T | 1 | a0010c0013t0010g0002 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.5435-5372G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47882895 | |||||||
chr3:47883926 | G | A | 3 | a0009c0009t0002g0046 a0009c0009t0002g0047 a0009c0009t0002g0048 |
3 | HG01891.hp2 HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.5435-6403C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47883926 | |||||||
chr3:47884148 | A | G | 1 | a0023c0022t0002g0088 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.5435-6625T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47884148 | |||||||
chr3:47884273 | G | T | 2 | a0010c0013t0010g0222 a0021c0028t0002g0224 |
2 | HG02145.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.5435-6750C>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47884273 | |||||||
chr3:47884493 | G | T | 3 | a0010c0013t0010g0002 a0010c0013t0010g0222 a0021c0028t0002g0224 |
3 | HG02145.hp2 HG02451.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.5435-6970C>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47884493 | |||||||
chr3:47884607 | A | T | 1 | a0009c0009t0002g0048 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.5435-7084T>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47884607 | |||||||
chr3:47884673 | C | T | 10 | a0005c0005t0003g0114 a0005c0005t0003g0115 a0005c0005t0003g0116 others(7): Show |
10 | HG00738.hp1 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.5435-7150G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47884673 | |||||||
chr3:47884774 | T | C | 3 | a0001c0001t0001g0168 a0001c0001t0001g0171 a0001c0001t0024g0165 |
3 | HG01169.hp1 HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.5435-7251A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47884774 | |||||||
chr3:47885244 | C | T | 1 | a0022c0030t0023g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.5435-7721G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47885244 | |||||||
chr3:47885367 | C | CATCA | 92 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(89): Show |
92 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.5435-7848_5435-784 others(8): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47885367 | |||||||
chr3:47885367 | CATCA | C | 6 | a0001c0001t0001g0147 a0002c0002t0002g0035 a0010c0013t0010g0002 others(3): Show |
6 | HG02145.hp2 HG02451.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.5435-7848_5435-784 others(8): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47885367 | |||||||
chr3:47885367 | CATCAATC others(5): Show |
C | 29 | a0003c0003t0003g0095 a0003c0003t0003g0098 a0003c0003t0003g0099 others(26): Show |
29 | HG00738.hp1 HG01109.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.5435-7856_5435-784 others(16): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47885367 | |||||||
chr3:47885396 | ATCAAT | A | 9 | a0002c0002t0002g0052 a0002c0002t0002g0089 a0002c0002t0002g0090 others(6): Show |
9 | HG02015.hp2 NA18747.hp1 NA18941.hp1 others(6): Show |
intron_variant | MODIFIER | c.5435-7878_5435-787 others(9): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47885396 | |||||||
chr3:47885737 | T | C | 2 | a0002c0002t0002g0030 a0002c0002t0002g0034 |
2 | NA19000.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.5435-8214A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47885737 | |||||||
chr3:47885792 | C | T | 124 | a0002c0002t0002g0001 a0002c0002t0002g0004 a0002c0002t0002g0005 others(121): Show |
125 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.5435-8269G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47885792 | |||||||
chr3:47885903 | C | T | 1 | a0010c0013t0010g0002 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.5435-8380G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47885903 | |||||||
chr3:47885965 | T | C | 1 | a0002c0002t0002g0051 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.5435-8442A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47885965 | |||||||
chr3:47885994 | T | C | 124 | a0002c0002t0002g0001 a0002c0002t0002g0004 a0002c0002t0002g0005 others(121): Show |
125 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.5435-8471A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47885994 | |||||||
chr3:47886070 | T | C | 1 | a0022c0030t0023g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.5435-8547A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47886070 | |||||||
chr3:47886342 | C | T | 1 | a0017c0026t0014g0148 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.5435-8819G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47886342 | |||||||
chr3:47886486 | G | A | 4 | a0007c0008t0006g0131 a0007c0008t0006g0149 a0007c0008t0006g0152 others(1): Show |
4 | HG01891.hp1 HG02970.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.5435-8963C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47886486 | |||||||
chr3:47886677 | C | T | 124 | a0002c0002t0002g0001 a0002c0002t0002g0004 a0002c0002t0002g0005 others(121): Show |
125 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.5435-9154G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47886677 | |||||||
chr3:47887212 | G | T | 1 | a0001c0001t0001g0179 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.5435-9689C>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47887212 | |||||||
chr3:47887225 | C | A | 1 | a0002c0002t0002g0051 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.5435-9702G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47887225 | |||||||
chr3:47887226 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.5435-9703G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47887226 | |||||||
chr3:47887262 | T | G | 1 | a0009c0009t0002g0046 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.5435-9739A>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47887262 | |||||||
chr3:47887296 | T | C | 122 | a0002c0002t0002g0001 a0002c0002t0002g0004 a0002c0002t0002g0005 others(119): Show |
123 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(120): Show |
intron_variant | MODIFIER | c.5435-9773A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47887296 | |||||||
chr3:47887424 | A | T | 1 | a0005c0005t0003g0122 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.5435-9901T>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47887424 | |||||||
chr3:47887524 | T | C | 124 | a0002c0002t0002g0001 a0002c0002t0002g0004 a0002c0002t0002g0005 others(121): Show |
125 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.5435-10001A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47887524 | |||||||
chr3:47887716 | A | T | 1 | a0004c0004t0020g0080 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.5435-10193T>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47887716 | |||||||
chr3:47888120 | C | G | 8 | a0004c0004t0002g0083 a0004c0004t0002g0084 a0004c0004t0002g0085 others(5): Show |
8 | HG02040.hp2 HG02071.hp2 HG02083.hp2 others(5): Show |
intron_variant | MODIFIER | c.5435-10597G>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47888120 | |||||||
chr3:47888179 | A | G | 1 | a0023c0022t0002g0088 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.5435-10656T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47888179 | |||||||
chr3:47888187 | C | A | 1 | a0001c0001t0016g0135 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.5435-10664G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47888187 | |||||||
chr3:47888206 | C | T | 10 | a0004c0004t0002g0083 a0004c0004t0002g0084 a0004c0004t0002g0085 others(7): Show |
10 | HG01934.hp1 HG02040.hp2 HG02071.hp2 others(7): Show |
intron_variant | MODIFIER | c.5435-10683G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47888206 | |||||||
chr3:47888215 | C | T | 1 | a0004c0004t0002g0084 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.5435-10692G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47888215 | |||||||
chr3:47888245 | A | G | 31 | a0002c0002t0002g0004 a0002c0002t0002g0005 a0002c0002t0002g0010 others(28): Show |
31 | HG00099.hp2 HG00597.hp2 HG00673.hp2 others(28): Show |
intron_variant | MODIFIER | c.5435-10722T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47888245 | |||||||
chr3:47888436 | C | G | 3 | a0009c0009t0002g0046 a0009c0009t0002g0047 a0009c0009t0002g0048 |
3 | HG01891.hp2 HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.5435-10913G>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47888436 | |||||||
chr3:47888438 | C | T | 1 | a0004c0004t0011g0049 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.5435-10915G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47888438 | |||||||
chr3:47888457 | G | A | 1 | a0002c0002t0005g0028 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.5435-10934C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47888457 | |||||||
chr3:47888459 | A | G | 1 | a0001c0001t0001g0184 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.5435-10936T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47888459 | |||||||
chr3:47888465 | C | T | 80 | a0002c0002t0002g0001 a0002c0002t0002g0004 a0002c0002t0002g0005 others(77): Show |
81 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.5435-10942G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47888465 | |||||||
chr3:47888550 | G | C | 1 | a0005c0005t0003g0122 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.5435-11027C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47888550 | |||||||
chr3:47888930 | C | G | 120 | a0002c0002t0002g0001 a0002c0002t0002g0004 a0002c0002t0002g0005 others(117): Show |
121 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(118): Show |
intron_variant | MODIFIER | c.5435-11407G>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47888930 | |||||||
chr3:47889299 | T | C | 1 | a0001c0001t0001g0227 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.5435-11776A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47889299 | |||||||
chr3:47889334 | C | T | 1 | a0023c0022t0002g0088 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.5435-11811G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47889334 | |||||||
chr3:47889594 | G | A | 2 | a0001c0001t0001g0162 a0001c0001t0001g0163 |
2 | NA18940.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.5435-12071C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47889594 | |||||||
chr3:47889875 | CCTCCATA others(18): Show |
C | 1 | a0022c0030t0023g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.5435-12377_5435-12 others(31): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47889875 | |||||||
chr3:47889927 | T | C | 1 | a0022c0030t0023g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.5435-12404A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47889927 | |||||||
chr3:47890037 | T | C | 1 | a0022c0030t0023g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.5435-12514A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47890037 | |||||||
chr3:47890283 | C | T | 2 | a0001c0001t0008g0166 a0001c0001t0008g0167 |
2 | HG02258.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.5434+12667G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47890283 | |||||||
chr3:47890489 | T | C | 1 | a0022c0030t0023g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.5434+12461A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47890489 | |||||||
chr3:47890494 | C | A | 124 | a0002c0002t0002g0001 a0002c0002t0002g0004 a0002c0002t0002g0005 others(121): Show |
125 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.5434+12456G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47890494 | |||||||
chr3:47890570 | T | C | 1 | a0023c0022t0002g0088 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.5434+12380A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47890570 | |||||||
chr3:47890784 | C | T | 124 | a0002c0002t0002g0001 a0002c0002t0002g0004 a0002c0002t0002g0005 others(121): Show |
125 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.5434+12166G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47890784 | |||||||
chr3:47890886 | C | G | 7 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0186 others(4): Show |
7 | NA18967.hp1 NA18969.hp1 NA19004.hp2 others(4): Show |
intron_variant | MODIFIER | c.5434+12064G>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47890886 | |||||||
chr3:47891083 | A | G | 1 | a0001c0001t0001g0176 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.5434+11867T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47891083 | |||||||
chr3:47891348 | T | A | 1 | a0006c0006t0002g0062 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.5434+11602A>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47891348 | |||||||
chr3:47891504 | A | C | 1 | a0002c0002t0002g0130 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.5434+11446T>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47891504 | |||||||
chr3:47891848 | G | A | 4 | a0002c0002t0002g0057 a0002c0002t0002g0058 a0002c0002t0002g0125 others(1): Show |
4 | HG02559.hp1 HG02976.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.5434+11102C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47891848 | |||||||
chr3:47891937 | G | T | 1 | a0001c0001t0001g0169 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.5434+11013C>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47891937 | |||||||
chr3:47892140 | C | T | 10 | a0005c0005t0003g0114 a0005c0005t0003g0115 a0005c0005t0003g0116 others(7): Show |
10 | HG00738.hp1 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.5434+10810G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47892140 | |||||||
chr3:47892358 | T | A | 1 | a0001c0001t0001g0127 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.5434+10592A>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47892358 | |||||||
chr3:47892398 | T | C | 1 | a0001c0001t0001g0183 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.5434+10552A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47892398 | |||||||
chr3:47892412 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.5434+10538G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47892412 | |||||||
chr3:47892452 | C | T | 1 | a0001c0001t0001g0230 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.5434+10498G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47892452 | |||||||
chr3:47892718 | C | G | 1 | a0002c0002t0002g0014 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.5434+10232G>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47892718 | |||||||
chr3:47893026 | T | TA | 101 | a0001c0001t0001g0169 a0001c0001t0001g0173 a0001c0001t0001g0195 others(98): Show |
102 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.5434+9923dupT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47893026 | |||||||
chr3:47893026 | T | TAA | 8 | a0002c0002t0002g0010 a0002c0002t0002g0033 a0002c0002t0002g0091 others(5): Show |
8 | HG00639.hp1 HG00733.hp1 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.5434+9922_5434+992 others(6): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47893026 | |||||||
chr3:47893050 | C | A | 1 | a0001c0001t0001g0132 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.5434+9900G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47893050 | |||||||
chr3:47893258 | C | T | 1 | a0005c0005t0003g0114 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.5434+9692G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47893258 | |||||||
chr3:47893500 | C | T | 3 | a0001c0001t0001g0134 a0001c0001t0001g0145 a0001c0001t0001g0146 |
3 | HG00639.hp2 HG00733.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.5434+9450G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47893500 | |||||||
chr3:47893672 | T | C | 1 | a0001c0001t0001g0209 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.5434+9278A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47893672 | |||||||
chr3:47893759 | CT | C | 17 | a0001c0001t0001g0154 a0001c0001t0001g0158 a0001c0001t0001g0168 others(14): Show |
17 | HG00099.hp2 HG01099.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.5434+9190delA | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47893759 | |||||||
chr3:47893774 | T | A | 11 | a0002c0002t0002g0021 a0002c0002t0002g0024 a0002c0002t0002g0025 others(8): Show |
11 | HG00099.hp2 HG01074.hp2 HG01346.hp2 others(8): Show |
intron_variant | MODIFIER | c.5434+9176A>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47893774 | |||||||
chr3:47893775 | A | T | 2 | a0001c0001t0008g0166 a0001c0001t0008g0167 |
2 | HG02258.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.5434+9175T>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47893775 | |||||||
chr3:47893783 | G | A | 2 | a0001c0001t0001g0191 a0001c0001t0001g0192 |
2 | HG04115.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.5434+9167C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47893783 | |||||||
chr3:47893813 | G | T | 124 | a0002c0002t0002g0001 a0002c0002t0002g0004 a0002c0002t0002g0005 others(121): Show |
125 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.5434+9137C>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47893813 | |||||||
chr3:47893933 | C | T | 1 | a0001c0001t0001g0208 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.5434+9017G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47893933 | |||||||
chr3:47893976 | C | A | 1 | a0001c0001t0001g0214 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.5434+8974G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47893976 | |||||||
chr3:47894074 | A | G | 1 | a0002c0002t0002g0027 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.5434+8876T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47894074 | |||||||
chr3:47894087 | G | C | 2 | a0010c0013t0010g0222 a0021c0028t0002g0224 |
2 | HG02145.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.5434+8863C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47894087 | |||||||
chr3:47894201 | T | C | 1 | a0002c0011t0002g0087 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.5434+8749A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47894201 | |||||||
chr3:47894302 | G | A | 2 | a0001c0001t0008g0166 a0001c0001t0008g0167 |
2 | HG02258.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.5434+8648C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47894302 | |||||||
chr3:47894478 | G | A | 3 | a0009c0009t0002g0046 a0009c0009t0002g0047 a0009c0009t0002g0048 |
3 | HG01891.hp2 HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.5434+8472C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47894478 | |||||||
chr3:47894562 | G | A | 8 | a0002c0002t0002g0045 a0002c0002t0002g0055 a0002c0002t0002g0056 others(5): Show |
8 | HG02559.hp1 HG02572.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.5434+8388C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47894562 | |||||||
chr3:47894600 | G | GA | 36 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0134 others(33): Show |
36 | HG00544.hp1 HG00609.hp2 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.5434+8349dupT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47894600 | |||||||
chr3:47894609 | T | C | 1 | a0003c0003t0003g0103 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.5434+8341A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47894609 | |||||||
chr3:47894716 | G | A | 1 | a0007c0008t0006g0131 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.5434+8234C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47894716 | |||||||
chr3:47895021 | C | CA | 35 | a0001c0001t0001g0229 a0003c0003t0003g0095 a0003c0003t0003g0098 others(32): Show |
35 | HG00738.hp1 HG01109.hp2 HG01884.hp1 others(32): Show |
intron_variant | MODIFIER | c.5434+7928dupT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47895021 | |||||||
chr3:47895181 | T | C | 171 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(168): Show |
172 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(169): Show |
intron_variant | MODIFIER | c.5434+7769A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47895181 | |||||||
chr3:47895530 | C | T | 2 | a0004c0004t0011g0049 a0004c0004t0011g0050 |
2 | HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.5434+7420G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47895530 | |||||||
chr3:47895582 | T | C | 124 | a0002c0002t0002g0001 a0002c0002t0002g0004 a0002c0002t0002g0005 others(121): Show |
125 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.5434+7368A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47895582 | |||||||
chr3:47896144 | G | A | 1 | a0023c0022t0002g0088 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.5434+6806C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47896144 | |||||||
chr3:47896864 | G | C | 119 | a0002c0002t0002g0001 a0002c0002t0002g0004 a0002c0002t0002g0005 others(116): Show |
120 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(117): Show |
intron_variant | MODIFIER | c.5434+6086C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47896864 | |||||||
chr3:47896895 | G | T | 29 | a0003c0003t0003g0095 a0003c0003t0003g0098 a0003c0003t0003g0099 others(26): Show |
29 | HG00738.hp1 HG01109.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.5434+6055C>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47896895 | |||||||
chr3:47897446 | C | T | 1 | a0004c0004t0002g0085 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.5434+5504G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47897446 | |||||||
chr3:47897528 | T | C | 26 | a0003c0003t0003g0095 a0003c0003t0003g0098 a0003c0003t0003g0099 others(23): Show |
26 | HG00738.hp1 HG01109.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.5434+5422A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47897528 | |||||||
chr3:47897704 | C | T | 3 | a0006c0006t0002g0074 a0006c0006t0002g0075 a0006c0006t0002g0076 |
3 | HG02602.hp1 HG02738.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.5434+5246G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47897704 | |||||||
chr3:47897891 | G | A | 1 | a0008c0010t0007g0111 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.5434+5059C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47897891 | |||||||
chr3:47897950 | G | GA | 13 | a0004c0004t0002g0083 a0004c0004t0002g0084 a0004c0004t0002g0085 others(10): Show |
13 | HG01934.hp1 HG02071.hp2 HG02083.hp2 others(10): Show |
intron_variant | MODIFIER | c.5434+4999dupT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47897950 | |||||||
chr3:47897951 | A | G | 15 | a0001c0001t0009g0178 a0003c0003t0003g0095 a0003c0003t0003g0098 others(12): Show |
15 | HG01109.hp2 HG02055.hp2 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.5434+4999T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47897951 | |||||||
chr3:47897952 | A | G | 2 | a0003c0003t0003g0110 a0023c0022t0002g0088 |
2 | HG02647.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.5434+4998T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47897952 | |||||||
chr3:47897953 | A | G | 1 | a0023c0022t0002g0088 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.5434+4997T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47897953 | |||||||
chr3:47897959 | A | G | 1 | a0001c0001t0001g0156 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.5434+4991T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47897959 | |||||||
chr3:47898136 | G | A | 90 | a0002c0002t0002g0001 a0002c0002t0002g0004 a0002c0002t0002g0005 others(87): Show |
91 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.5434+4814C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47898136 | |||||||
chr3:47898426 | C | T | 3 | a0009c0009t0002g0046 a0009c0009t0002g0047 a0009c0009t0002g0048 |
3 | HG01891.hp2 HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.5434+4524G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47898426 | |||||||
chr3:47898494 | C | T | 1 | a0010c0013t0010g0002 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.5434+4456G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47898494 | |||||||
chr3:47898495 | C | T | 29 | a0003c0003t0003g0095 a0003c0003t0003g0098 a0003c0003t0003g0099 others(26): Show |
29 | HG00738.hp1 HG01109.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.5434+4455G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47898495 | |||||||
chr3:47898500 | C | CA | 5 | a0001c0001t0001g0159 a0001c0001t0001g0198 a0001c0001t0022g0213 others(2): Show |
5 | HG02486.hp2 HG02647.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.5434+4449dupT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47898500 | |||||||
chr3:47898929 | C | T | 1 | a0022c0030t0023g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.5434+4021G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47898929 | |||||||
chr3:47899239 | G | A | 1 | a0002c0002t0002g0066 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.5434+3711C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47899239 | |||||||
chr3:47899744 | G | A | 1 | a0006c0006t0002g0062 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.5434+3206C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47899744 | |||||||
chr3:47900126 | T | C | 3 | a0010c0013t0010g0002 a0010c0013t0010g0222 a0021c0028t0002g0224 |
3 | HG02145.hp2 HG02451.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.5434+2824A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47900126 | |||||||
chr3:47900304 | T | C | 1 | a0004c0004t0020g0080 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.5434+2646A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47900304 | |||||||
chr3:47900858 | A | G | 1 | a0022c0030t0023g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.5434+2092T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47900858 | |||||||
chr3:47901072 | C | T | 10 | a0005c0005t0003g0114 a0005c0005t0003g0115 a0005c0005t0003g0116 others(7): Show |
10 | HG00738.hp1 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.5434+1878G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47901072 | |||||||
chr3:47901184 | A | G | 1 | a0002c0002t0004g0017 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.5434+1766T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47901184 | |||||||
chr3:47901442 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.5434+1508C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47901442 | |||||||
chr3:47901759 | C | G | 1 | a0005c0005t0003g0115 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.5434+1191G>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47901759 | |||||||
chr3:47902123 | C | T | 16 | a0003c0003t0003g0095 a0003c0003t0003g0098 a0003c0003t0003g0099 others(13): Show |
16 | HG01109.hp2 HG02055.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.5434+827G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47902123 | |||||||
chr3:47902371 | T | C | 90 | a0002c0002t0002g0001 a0002c0002t0002g0004 a0002c0002t0002g0005 others(87): Show |
91 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.5434+579A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47902371 | |||||||
chr3:47902415 | C | T | 1 | a0002c0002t0002g0036 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.5434+535G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47902415 | |||||||
chr3:47902430 | C | T | 1 | a0001c0001t0001g0043 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.5434+520G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47902430 | |||||||
chr3:47902673 | C | CA | 38 | a0001c0001t0001g0042 a0001c0001t0001g0137 a0001c0001t0001g0141 others(35): Show |
38 | HG00597.hp1 HG00738.hp1 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.5434+276dupT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47902673 | |||||||
chr3:47902673 | C | CAA | 36 | a0001c0001t0001g0181 a0001c0001t0001g0198 a0001c0001t0001g0207 others(33): Show |
36 | HG00673.hp2 HG00735.hp1 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.5434+275_5434+276d others(4): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47902673 | |||||||
chr3:47902673 | C | CAAA | 34 | a0001c0001t0001g0154 a0001c0001t0001g0188 a0002c0002t0002g0001 others(31): Show |
35 | HG00099.hp2 HG00544.hp2 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.5434+274_5434+276d others(5): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47902673 | |||||||
chr3:47902673 | C | CAAAA | 16 | a0002c0002t0002g0034 a0002c0002t0002g0052 a0002c0002t0002g0057 others(13): Show |
16 | HG00280.hp2 HG01123.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.5434+273_5434+276d others(6): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47902673 | |||||||
chr3:47902673 | CA | C | 5 | a0001c0001t0001g0041 a0001c0001t0001g0200 a0001c0001t0001g0201 others(2): Show |
5 | HG00673.hp1 HG02486.hp1 NA18747.hp2 others(2): Show |
intron_variant | MODIFIER | c.5434+276delT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47902673 | |||||||
chr3:47902673 | CAAAAAAA others(4): Show |
C | 1 | a0015c0021t0002g0011 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.5434+266_5434+276d others(13): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | 47902673 | |||||||
chr3:47903146 | AG | A | 120 | a0002c0002t0002g0001 a0002c0002t0002g0004 a0002c0002t0002g0005 others(117): Show |
121 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(118): Show |
intron_variant | MODIFIER | c.5384-147delC | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47903146 | |||||||
chr3:47903156 | C | T | 1 | a0017c0026t0014g0148 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.5384-156G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47903156 | |||||||
chr3:47903254 | C | A | 3 | a0009c0009t0002g0046 a0009c0009t0002g0047 a0009c0009t0002g0048 |
3 | HG01891.hp2 HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.5384-254G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47903254 | |||||||
chr3:47903532 | C | CA | 21 | a0001c0001t0001g0160 a0001c0001t0001g0180 a0001c0001t0001g0191 others(18): Show |
21 | HG00741.hp1 HG01934.hp1 HG02040.hp2 others(18): Show |
intron_variant | MODIFIER | c.5384-533dupT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47903532 | |||||||
chr3:47903532 | CA | C | 5 | a0001c0001t0001g0214 a0002c0002t0002g0004 a0002c0002t0002g0005 others(2): Show |
5 | HG01981.hp2 NA18952.hp1 NA18998.hp1 others(2): Show |
intron_variant | MODIFIER | c.5384-533delT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47903532 | |||||||
chr3:47903572 | G | C | 1 | a0023c0022t0002g0088 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.5384-572C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47903572 | |||||||
chr3:47903661 | A | C | 1 | a0002c0002t0004g0017 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.5384-661T>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47903661 | |||||||
chr3:47904043 | A | G | 1 | a0001c0001t0001g0160 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.5384-1043T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47904043 | |||||||
chr3:47904235 | A | G | 3 | a0009c0009t0002g0046 a0009c0009t0002g0047 a0009c0009t0002g0048 |
3 | HG01891.hp2 HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.5384-1235T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47904235 | |||||||
chr3:47904327 | A | T | 91 | a0002c0002t0002g0001 a0002c0002t0002g0004 a0002c0002t0002g0005 others(88): Show |
92 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.5384-1327T>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47904327 | |||||||
chr3:47904461 | G | A | 1 | a0010c0013t0010g0002 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.5384-1461C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47904461 | |||||||
chr3:47904582 | T | G | 1 | a0001c0001t0009g0178 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.5384-1582A>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47904582 | |||||||
chr3:47905218 | T | C | 80 | a0002c0002t0002g0001 a0002c0002t0002g0004 a0002c0002t0002g0005 others(77): Show |
81 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.5384-2218A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47905218 | |||||||
chr3:47905343 | A | G | 1 | a0002c0002t0002g0036 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.5384-2343T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47905343 | |||||||
chr3:47905479 | G | A | 6 | a0004c0004t0002g0083 a0004c0004t0002g0084 a0004c0004t0002g0085 others(3): Show |
6 | HG02040.hp2 HG02071.hp2 HG02083.hp2 others(3): Show |
intron_variant | MODIFIER | c.5384-2479C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47905479 | |||||||
chr3:47905524 | A | G | 1 | a0001c0001t0001g0179 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.5384-2524T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47905524 | |||||||
chr3:47905545 | C | A | 1 | a0020c0023t0002g0053 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.5384-2545G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47905545 | |||||||
chr3:47905548 | A | C | 18 | a0001c0001t0001g0137 a0001c0001t0001g0159 a0001c0001t0001g0185 others(15): Show |
18 | HG00544.hp2 HG01891.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.5384-2548T>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47905548 | |||||||
chr3:47905551 | A | C | 1 | a0010c0013t0010g0222 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.5384-2551T>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47905551 | |||||||
chr3:47905558 | C | A | 1 | a0001c0001t0002g0150 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.5384-2558G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47905558 | |||||||
chr3:47905688 | G | A | 1 | a0005c0005t0003g0116 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.5384-2688C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47905688 | |||||||
chr3:47905691 | AC | A | 124 | a0002c0002t0002g0001 a0002c0002t0002g0004 a0002c0002t0002g0005 others(121): Show |
125 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.5384-2692delG | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47905691 | |||||||
chr3:47905694 | A | T | 124 | a0002c0002t0002g0001 a0002c0002t0002g0004 a0002c0002t0002g0005 others(121): Show |
125 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.5384-2694T>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47905694 | |||||||
chr3:47905734 | C | T | 7 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(4): Show |
7 | HG01074.hp1 HG01169.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.5384-2734G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47905734 | |||||||
chr3:47905855 | G | A | 1 | a0022c0030t0023g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.5384-2855C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47905855 | |||||||
chr3:47906031 | A | C | 3 | a0006c0006t0002g0074 a0006c0006t0002g0075 a0006c0006t0002g0076 |
3 | HG02602.hp1 HG02738.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.5383+3007T>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47906031 | |||||||
chr3:47906084 | C | CA | 31 | a0001c0001t0001g0042 a0001c0001t0001g0158 a0001c0001t0001g0191 others(28): Show |
31 | HG00738.hp1 HG01109.hp2 HG01516.hp2 others(28): Show |
intron_variant | MODIFIER | c.5383+2953dupT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47906084 | |||||||
chr3:47906084 | C | CAA | 7 | a0003c0003t0003g0107 a0005c0005t0003g0114 a0005c0005t0003g0115 others(4): Show |
7 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.5383+2952_5383+295 others(6): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47906084 | |||||||
chr3:47906247 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.5383+2791G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47906247 | |||||||
chr3:47906596 | TC | T | 2 | a0002c0002t0004g0015 a0002c0002t0004g0016 |
2 | NA19005.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.5383+2441delG | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47906596 | |||||||
chr3:47906623 | C | T | 3 | a0010c0013t0010g0002 a0010c0013t0010g0222 a0021c0028t0002g0224 |
3 | HG02145.hp2 HG02451.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.5383+2415G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47906623 | |||||||
chr3:47906795 | T | TA | 32 | a0001c0001t0001g0147 a0002c0002t0013g0065 a0003c0003t0003g0095 others(29): Show |
32 | HG00738.hp1 HG01109.hp2 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.5383+2242dupT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47906795 | |||||||
chr3:47906808 | A | C | 1 | a0002c0002t0002g0066 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.5383+2230T>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47906808 | |||||||
chr3:47906874 | G | T | 124 | a0002c0002t0002g0001 a0002c0002t0002g0004 a0002c0002t0002g0005 others(121): Show |
125 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.5383+2164C>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47906874 | |||||||
chr3:47906985 | A | G | 224 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(221): Show |
225 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(222): Show |
intron_variant | MODIFIER | c.5383+2053T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47906985 | |||||||
chr3:47907077 | C | T | 2 | a0001c0001t0008g0166 a0001c0001t0008g0167 |
2 | HG02258.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.5383+1961G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47907077 | |||||||
chr3:47907087 | G | A | 1 | a0004c0004t0002g0085 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.5383+1951C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47907087 | |||||||
chr3:47907420 | T | A | 4 | a0001c0007t0001g0219 a0004c0004t0002g0223 a0005c0005t0003g0114 others(1): Show |
4 | HG02040.hp2 HG02071.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.5383+1618A>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47907420 | |||||||
chr3:47907590 | A | G | 1 | a0002c0002t0002g0052 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.5383+1448T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47907590 | |||||||
chr3:47908048 | G | GT | 80 | a0002c0002t0002g0001 a0002c0002t0002g0004 a0002c0002t0002g0005 others(77): Show |
81 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.5383+989dupA | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47908048 | |||||||
chr3:47908185 | C | A | 1 | a0001c0001t0002g0150 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.5383+853G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47908185 | |||||||
chr3:47908229 | C | T | 1 | a0001c0001t0001g0156 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.5383+809G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47908229 | |||||||
chr3:47908841 | C | A | 1 | a0020c0023t0002g0053 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.5383+197G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 9/20 | chr3 | 47908841 | |||||||
chr3:47912447 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.2000-26G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 8/20 | chr3 | 47912447 | |||||||
chr3:47913836 | A | G | 1 | a0021c0028t0002g0224 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1999+981T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 8/20 | chr3 | 47913836 | |||||||
chr3:47913977 | A | T | 4 | a0001c0007t0001g0218 a0001c0007t0001g0219 a0001c0007t0001g0220 others(1): Show |
4 | HG02451.hp1 HG02572.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1999+840T>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 8/20 | chr3 | 47913977 | |||||||
chr3:47914511 | T | C | 1 | a0001c0001t0001g0179 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1999+306A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 8/20 | chr3 | 47914511 | |||||||
chr3:47915016 | T | C | 80 | a0002c0002t0002g0001 a0002c0002t0002g0004 a0002c0002t0002g0005 others(77): Show |
81 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.1877-77A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 7/20 | chr3 | 47915016 | |||||||
chr3:47915035 | G | A | 8 | a0001c0001t0001g0157 a0001c0001t0001g0162 a0001c0001t0001g0163 others(5): Show |
8 | HG00544.hp1 HG00609.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.1877-96C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 7/20 | chr3 | 47915035 | |||||||
chr3:47915070 | G | A | 1 | a0002c0002t0004g0003 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1877-131C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 7/20 | chr3 | 47915070 | |||||||
chr3:47915174 | T | C | 1 | a0002c0020t0002g0054 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1877-235A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 7/20 | chr3 | 47915174 | |||||||
chr3:47915179 | C | T | 4 | a0002c0002t0002g0052 a0002c0002t0002g0094 a0002c0002t0002g0118 others(1): Show |
4 | HG02015.hp2 NA18747.hp1 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.1877-240G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 7/20 | chr3 | 47915179 | |||||||
chr3:47915185 | C | T | 2 | a0001c0001t0001g0147 a0001c0001t0001g0156 |
2 | HG03831.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1877-246G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 7/20 | chr3 | 47915185 | |||||||
chr3:47915202 | C | T | 1 | a0001c0001t0001g0214 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1877-263G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 7/20 | chr3 | 47915202 | |||||||
chr3:47915382 | C | A | 1 | a0001c0001t0001g0129 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1877-443G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 7/20 | chr3 | 47915382 | |||||||
chr3:47915435 | T | C | 1 | a0001c0001t0001g0156 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1877-496A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 7/20 | chr3 | 47915435 | |||||||
chr3:47915541 | C | T | 1 | a0023c0022t0002g0088 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1876+410G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 7/20 | chr3 | 47915541 | |||||||
chr3:47915629 | G | C | 4 | a0002c0002t0002g0052 a0002c0002t0002g0094 a0002c0002t0002g0118 others(1): Show |
4 | HG02015.hp2 NA18747.hp1 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.1876+322C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 7/20 | chr3 | 47915629 | |||||||
chr3:47915725 | T | C | 2 | a0002c0002t0002g0029 a0002c0002t0002g0032 |
2 | HG00544.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.1876+226A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 7/20 | chr3 | 47915725 | |||||||
chr3:47915799 | G | A | 3 | a0010c0013t0010g0002 a0010c0013t0010g0222 a0021c0028t0002g0224 |
3 | HG02145.hp2 HG02451.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1876+152C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 7/20 | chr3 | 47915799 | |||||||
chr3:47915867 | T | G | 1 | a0002c0002t0013g0065 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1876+84A>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 7/20 | chr3 | 47915867 | |||||||
chr3:47917518 | G | A | 1 | a0001c0001t0001g0225 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.653-344C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 6/20 | chr3 | 47917518 | |||||||
chr3:47917544 | G | T | 1 | a0001c0001t0001g0147 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.653-370C>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 6/20 | chr3 | 47917544 | |||||||
chr3:47917585 | C | CA | 8 | a0001c0001t0001g0043 a0001c0001t0001g0127 a0001c0001t0001g0136 others(5): Show |
8 | HG02559.hp2 HG02630.hp2 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.653-412dupT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 6/20 | chr3 | 47917585 | |||||||
chr3:47917585 | CA | C | 120 | a0001c0001t0001g0216 a0002c0002t0002g0001 a0002c0002t0002g0004 others(117): Show |
121 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(118): Show |
intron_variant | MODIFIER | c.653-412delT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 6/20 | chr3 | 47917585 | |||||||
chr3:47917605 | G | A | 1 | a0004c0004t0011g0050 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.653-431C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 6/20 | chr3 | 47917605 | |||||||
chr3:47918196 | C | G | 1 | a0002c0002t0002g0057 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.652+523G>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 6/20 | chr3 | 47918196 | |||||||
chr3:47918280 | A | G | 124 | a0002c0002t0002g0001 a0002c0002t0002g0004 a0002c0002t0002g0005 others(121): Show |
125 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.652+439T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 6/20 | chr3 | 47918280 | |||||||
chr3:47918479 | GA | G | 3 | a0009c0009t0002g0046 a0009c0009t0002g0047 a0009c0009t0002g0048 |
3 | HG01891.hp2 HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.652+239delT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 6/20 | chr3 | 47918479 | |||||||
chr3:47918485 | A | AAT | 3 | a0010c0013t0010g0002 a0010c0013t0010g0222 a0021c0028t0002g0224 |
3 | HG02145.hp2 HG02451.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.652+232_652+233dup others(2): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 6/20 | chr3 | 47918485 | |||||||
chr3:47918487 | T | A | 11 | a0001c0007t0001g0219 a0005c0005t0003g0114 a0005c0005t0003g0115 others(8): Show |
11 | HG00738.hp1 HG01884.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.652+232A>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 6/20 | chr3 | 47918487 | |||||||
chr3:47919021 | T | A | 80 | a0002c0002t0002g0001 a0002c0002t0002g0004 a0002c0002t0002g0005 others(77): Show |
81 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.530-180A>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 5/20 | chr3 | 47919021 | |||||||
chr3:47919040 | T | C | 1 | a0023c0022t0002g0088 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.530-199A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 5/20 | chr3 | 47919040 | |||||||
chr3:47919119 | G | C | 1 | a0022c0030t0023g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.530-278C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 5/20 | chr3 | 47919119 | |||||||
chr3:47919142 | C | T | 1 | a0001c0001t0001g0229 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.530-301G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 5/20 | chr3 | 47919142 | |||||||
chr3:47919143 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.530-302C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 5/20 | chr3 | 47919143 | |||||||
chr3:47919210 | C | T | 2 | a0007c0008t0006g0131 a0007c0008t0006g0226 |
2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.530-369G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 5/20 | chr3 | 47919210 | |||||||
chr3:47919285 | C | A | 1 | a0023c0022t0002g0088 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.530-444G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 5/20 | chr3 | 47919285 | |||||||
chr3:47919356 | G | A | 3 | a0008c0010t0007g0111 a0008c0010t0007g0112 a0008c0010t0007g0113 |
3 | HG00738.hp1 HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.530-515C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 5/20 | chr3 | 47919356 | |||||||
chr3:47919410 | C | T | 4 | a0001c0007t0001g0218 a0001c0007t0001g0219 a0001c0007t0001g0220 others(1): Show |
4 | HG02451.hp1 HG02572.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.530-569G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 5/20 | chr3 | 47919410 | |||||||
chr3:47919443 | G | T | 1 | a0010c0013t0010g0002 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.530-602C>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 5/20 | chr3 | 47919443 | |||||||
chr3:47919530 | G | C | 1 | a0020c0023t0002g0053 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.530-689C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 5/20 | chr3 | 47919530 | |||||||
chr3:47919541 | C | T | 1 | a0023c0022t0002g0088 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.530-700G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 5/20 | chr3 | 47919541 | |||||||
chr3:47919569 | A | G | 1 | a0002c0002t0002g0025 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.530-728T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 5/20 | chr3 | 47919569 | |||||||
chr3:47919601 | C | T | 3 | a0002c0002t0002g0123 a0002c0011t0002g0073 a0002c0011t0002g0087 |
3 | HG00639.hp1 HG00733.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.530-760G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 5/20 | chr3 | 47919601 | |||||||
chr3:47919916 | T | TTTG | 4 | a0001c0001t0001g0134 a0001c0001t0001g0144 a0001c0001t0001g0145 others(1): Show |
4 | HG00639.hp2 HG00733.hp2 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.530-1078_530-1076d others(5): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 5/20 | chr3 | 47919916 | |||||||
chr3:47919916 | TTTG | T | 121 | a0002c0002t0002g0001 a0002c0002t0002g0004 a0002c0002t0002g0005 others(118): Show |
122 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.530-1078_530-1076d others(5): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 5/20 | chr3 | 47919916 | |||||||
chr3:47920114 | G | C | 47 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(44): Show |
47 | HG00544.hp1 HG00609.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.530-1273C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 5/20 | chr3 | 47920114 | |||||||
chr3:47920136 | A | C | 7 | a0002c0002t0002g0004 a0002c0002t0002g0005 a0002c0002t0002g0021 others(4): Show |
7 | HG00099.hp2 HG00673.hp2 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.530-1295T>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 5/20 | chr3 | 47920136 | |||||||
chr3:47920191 | G | C | 1 | a0003c0003t0003g0102 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.530-1350C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 5/20 | chr3 | 47920191 | |||||||
chr3:47920253 | G | T | 1 | a0002c0002t0002g0066 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.530-1412C>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 5/20 | chr3 | 47920253 | |||||||
chr3:47920354 | G | A | 9 | a0002c0002t0002g0052 a0002c0002t0002g0089 a0002c0002t0002g0090 others(6): Show |
9 | HG02015.hp2 NA18747.hp1 NA18941.hp1 others(6): Show |
intron_variant | MODIFIER | c.529+1411C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 5/20 | chr3 | 47920354 | |||||||
chr3:47920542 | T | C | 1 | a0004c0004t0020g0080 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.529+1223A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 5/20 | chr3 | 47920542 | |||||||
chr3:47920544 | GT | G | 158 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0126 others(155): Show |
159 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(156): Show |
intron_variant | MODIFIER | c.529+1220delA | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 5/20 | chr3 | 47920544 | |||||||
chr3:47920544 | GTT | G | 13 | a0001c0001t0001g0159 a0001c0001t0001g0173 a0001c0001t0001g0174 others(10): Show |
13 | HG00597.hp1 HG02071.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.529+1219_529+1220d others(4): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 5/20 | chr3 | 47920544 | |||||||
chr3:47920568 | T | A | 14 | a0003c0003t0003g0095 a0003c0003t0003g0098 a0003c0003t0003g0099 others(11): Show |
14 | HG01109.hp2 HG02055.hp2 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.529+1197A>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 5/20 | chr3 | 47920568 | |||||||
chr3:47920702 | C | G | 1 | a0004c0004t0011g0049 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.529+1063G>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 5/20 | chr3 | 47920702 | |||||||
chr3:47920945 | C | G | 1 | a0004c0004t0011g0050 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.529+820G>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 5/20 | chr3 | 47920945 | |||||||
chr3:47921542 | C | A | 1 | a0022c0030t0023g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.529+223G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 5/20 | chr3 | 47921542 | |||||||
chr3:47922565 | TA | T | 121 | a0002c0002t0002g0001 a0002c0002t0002g0004 a0002c0002t0002g0005 others(118): Show |
122 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.416-688delT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 4/20 | chr3 | 47922565 | |||||||
chr3:47922764 | G | A | 1 | a0001c0001t0009g0178 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.416-886C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 4/20 | chr3 | 47922764 | |||||||
chr3:47922766 | A | G | 1 | a0021c0028t0002g0224 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.416-888T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 4/20 | chr3 | 47922766 | |||||||
chr3:47922818 | G | A | 3 | a0010c0013t0010g0002 a0010c0013t0010g0222 a0021c0028t0002g0224 |
3 | HG02145.hp2 HG02451.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.416-940C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 4/20 | chr3 | 47922818 | |||||||
chr3:47922921 | G | A | 1 | a0001c0001t0001g0230 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.416-1043C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 4/20 | chr3 | 47922921 | |||||||
chr3:47922974 | C | T | 1 | a0017c0026t0014g0148 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.416-1096G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 4/20 | chr3 | 47922974 | |||||||
chr3:47922999 | G | A | 3 | a0010c0013t0010g0002 a0010c0013t0010g0222 a0021c0028t0002g0224 |
3 | HG02145.hp2 HG02451.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.416-1121C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 4/20 | chr3 | 47922999 | |||||||
chr3:47923024 | T | G | 9 | a0002c0002t0002g0052 a0002c0002t0002g0089 a0002c0002t0002g0090 others(6): Show |
9 | HG02015.hp2 NA18747.hp1 NA18941.hp1 others(6): Show |
intron_variant | MODIFIER | c.416-1146A>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 4/20 | chr3 | 47923024 | |||||||
chr3:47923347 | T | C | 3 | a0009c0009t0002g0046 a0009c0009t0002g0047 a0009c0009t0002g0048 |
3 | HG01891.hp2 HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.416-1469A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 4/20 | chr3 | 47923347 | |||||||
chr3:47923623 | T | TA | 12 | a0001c0001t0001g0139 a0001c0001t0001g0163 a0001c0001t0001g0164 others(9): Show |
12 | HG00733.hp1 HG00741.hp2 HG02148.hp1 others(9): Show |
intron_variant | MODIFIER | c.416-1746dupT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 4/20 | chr3 | 47923623 | |||||||
chr3:47923638 | C | A | 4 | a0001c0007t0001g0218 a0001c0007t0001g0219 a0002c0002t0002g0092 others(1): Show |
4 | HG02572.hp1 HG02647.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.416-1760G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 4/20 | chr3 | 47923638 | |||||||
chr3:47923685 | G | A | 16 | a0003c0003t0003g0095 a0003c0003t0003g0098 a0003c0003t0003g0099 others(13): Show |
16 | HG01109.hp2 HG02055.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.416-1807C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 4/20 | chr3 | 47923685 | |||||||
chr3:47924715 | T | C | 2 | a0004c0004t0011g0049 a0004c0004t0011g0050 |
2 | HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.416-2837A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 4/20 | chr3 | 47924715 | |||||||
chr3:47924816 | A | AT | 125 | a0001c0001t0001g0187 a0002c0002t0002g0001 a0002c0002t0002g0004 others(122): Show |
126 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.416-2939dupA | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 4/20 | chr3 | 47924816 | |||||||
chr3:47924959 | C | T | 119 | a0002c0002t0002g0001 a0002c0002t0002g0004 a0002c0002t0002g0005 others(116): Show |
120 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(117): Show |
intron_variant | MODIFIER | c.416-3081G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 4/20 | chr3 | 47924959 | |||||||
chr3:47925270 | G | A | 1 | a0001c0001t0001g0186 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.415+2958C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 4/20 | chr3 | 47925270 | |||||||
chr3:47925583 | G | A | 1 | a0003c0003t0003g0095 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.415+2645C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 4/20 | chr3 | 47925583 | |||||||
chr3:47925629 | A | G | 16 | a0003c0003t0003g0095 a0003c0003t0003g0098 a0003c0003t0003g0099 others(13): Show |
16 | HG01109.hp2 HG02055.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.415+2599T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 4/20 | chr3 | 47925629 | |||||||
chr3:47925713 | G | C | 2 | a0004c0004t0011g0049 a0004c0004t0011g0050 |
2 | HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.415+2515C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 4/20 | chr3 | 47925713 | |||||||
chr3:47925747 | T | C | 1 | a0022c0030t0023g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.415+2481A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 4/20 | chr3 | 47925747 | |||||||
chr3:47925824 | G | A | 1 | a0021c0028t0002g0224 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.415+2404C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 4/20 | chr3 | 47925824 | |||||||
chr3:47925924 | G | A | 1 | a0002c0002t0002g0051 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.415+2304C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 4/20 | chr3 | 47925924 | |||||||
chr3:47926076 | G | A | 1 | a0002c0002t0002g0082 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.415+2152C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 4/20 | chr3 | 47926076 | |||||||
chr3:47926253 | G | A | 1 | a0022c0030t0023g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.415+1975C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 4/20 | chr3 | 47926253 | |||||||
chr3:47926287 | G | A | 1 | a0002c0002t0004g0017 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.415+1941C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 4/20 | chr3 | 47926287 | |||||||
chr3:47926580 | G | A | 16 | a0003c0003t0003g0095 a0003c0003t0003g0098 a0003c0003t0003g0099 others(13): Show |
16 | HG01109.hp2 HG02055.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.415+1648C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 4/20 | chr3 | 47926580 | |||||||
chr3:47926811 | C | T | 1 | a0001c0001t0009g0178 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.415+1417G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 4/20 | chr3 | 47926811 | |||||||
chr3:47926881 | T | C | 6 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0002c0002t0005g0026 others(3): Show |
6 | HG01074.hp2 HG01346.hp2 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.415+1347A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 4/20 | chr3 | 47926881 | |||||||
chr3:47927022 | T | C | 1 | a0008c0010t0007g0111 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.415+1206A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 4/20 | chr3 | 47927022 | |||||||
chr3:47927062 | G | C | 15 | a0003c0003t0003g0095 a0003c0003t0003g0098 a0003c0003t0003g0099 others(12): Show |
15 | HG01109.hp2 HG02055.hp2 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.415+1166C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 4/20 | chr3 | 47927062 | |||||||
chr3:47927158 | C | CA | 87 | a0001c0001t0001g0147 a0001c0001t0001g0159 a0001c0001t0001g0173 others(84): Show |
87 | HG00544.hp2 HG00597.hp2 HG00673.hp2 others(84): Show |
intron_variant | MODIFIER | c.415+1069dupT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 4/20 | chr3 | 47927158 | |||||||
chr3:47927158 | C | CAA | 42 | a0002c0002t0002g0001 a0002c0002t0002g0025 a0002c0002t0002g0030 others(39): Show |
43 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.415+1068_415+1069d others(4): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 4/20 | chr3 | 47927158 | |||||||
chr3:47927507 | C | T | 1 | a0001c0001t0001g0128 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.415+721G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 4/20 | chr3 | 47927507 | |||||||
chr3:47927822 | T | C | 1 | a0001c0001t0001g0147 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.415+406A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 4/20 | chr3 | 47927822 | |||||||
chr3:47927855 | GT | G | 2 | a0012c0012t0002g0071 a0012c0012t0002g0078 |
2 | HG04115.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.415+372delA | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 4/20 | chr3 | 47927855 | |||||||
chr3:47928577 | C | T | 1 | a0001c0001t0024g0165 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.293-227G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47928577 | |||||||
chr3:47928619 | C | T | 120 | a0002c0002t0002g0001 a0002c0002t0002g0004 a0002c0002t0002g0005 others(117): Show |
121 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(118): Show |
intron_variant | MODIFIER | c.293-269G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47928619 | |||||||
chr3:47928647 | T | C | 1 | a0002c0002t0002g0022 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.293-297A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47928647 | |||||||
chr3:47928812 | C | T | 1 | a0004c0004t0002g0084 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.293-462G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47928812 | |||||||
chr3:47928840 | G | A | 4 | a0003c0003t0003g0102 a0003c0003t0003g0104 a0003c0003t0003g0108 others(1): Show |
4 | HG02922.hp1 HG02965.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.293-490C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47928840 | |||||||
chr3:47929312 | C | A | 1 | a0005c0005t0003g0114 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.293-962G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47929312 | |||||||
chr3:47929376 | G | A | 3 | a0001c0001t0001g0134 a0001c0001t0001g0145 a0001c0001t0001g0146 |
3 | HG00639.hp2 HG00733.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.293-1026C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47929376 | |||||||
chr3:47929563 | A | G | 8 | a0002c0002t0002g0045 a0002c0002t0002g0055 a0002c0002t0002g0056 others(5): Show |
8 | HG02559.hp1 HG02572.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.293-1213T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47929563 | |||||||
chr3:47929627 | C | CA | 24 | a0001c0001t0001g0126 a0001c0001t0001g0129 a0001c0001t0001g0132 others(21): Show |
24 | HG00609.hp1 HG00673.hp1 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.293-1278dupT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47929627 | |||||||
chr3:47929627 | CA | C | 34 | a0001c0001t0001g0042 a0001c0001t0001g0171 a0001c0001t0001g0184 others(31): Show |
34 | HG00597.hp2 HG01123.hp2 HG02145.hp1 others(31): Show |
intron_variant | MODIFIER | c.293-1278delT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47929627 | |||||||
chr3:47929627 | CAA | C | 48 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0012 others(45): Show |
49 | HG00280.hp2 HG00639.hp1 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.293-1279_293-1278d others(4): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47929627 | |||||||
chr3:47929627 | CAAA | C | 37 | a0002c0002t0002g0004 a0002c0002t0002g0010 a0002c0002t0002g0013 others(34): Show |
37 | HG00099.hp2 HG00544.hp2 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.293-1280_293-1278d others(5): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47929627 | |||||||
chr3:47929627 | CAAAA | C | 6 | a0004c0004t0002g0084 a0004c0004t0002g0085 a0004c0004t0002g0223 others(3): Show |
6 | HG02040.hp2 HG02071.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.293-1281_293-1278d others(6): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47929627 | |||||||
chr3:47929627 | CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0001g0170 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.293-1289_293-1278d others(14): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47929627 | |||||||
chr3:47929822 | T | C | 1 | a0001c0001t0001g0186 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.293-1472A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47929822 | |||||||
chr3:47929958 | A | G | 120 | a0002c0002t0002g0001 a0002c0002t0002g0004 a0002c0002t0002g0005 others(117): Show |
121 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(118): Show |
intron_variant | MODIFIER | c.293-1608T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47929958 | |||||||
chr3:47930031 | G | A | 1 | a0010c0013t0010g0002 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.293-1681C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47930031 | |||||||
chr3:47930124 | G | A | 2 | a0002c0002t0002g0030 a0002c0002t0002g0034 |
2 | NA19000.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.293-1774C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47930124 | |||||||
chr3:47930125 | C | T | 1 | a0022c0030t0023g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.293-1775G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47930125 | |||||||
chr3:47930167 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.293-1817G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47930167 | |||||||
chr3:47930174 | G | A | 1 | a0021c0028t0002g0224 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.293-1824C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47930174 | |||||||
chr3:47930186 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.293-1836G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47930186 | |||||||
chr3:47930308 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.293-1958C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47930308 | |||||||
chr3:47930374 | A | G | 1 | a0001c0001t0001g0042 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.293-2024T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47930374 | |||||||
chr3:47930414 | C | T | 1 | a0028c0017t0002g0038 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.293-2064G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47930414 | |||||||
chr3:47930459 | A | C | 1 | a0010c0013t0010g0222 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.293-2109T>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47930459 | |||||||
chr3:47930475 | C | A | 123 | a0002c0002t0002g0001 a0002c0002t0002g0004 a0002c0002t0002g0005 others(120): Show |
124 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(121): Show |
intron_variant | MODIFIER | c.293-2125G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47930475 | |||||||
chr3:47930789 | C | T | 2 | a0003c0003t0003g0100 a0022c0030t0023g0044 |
2 | HG02486.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.293-2439G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47930789 | |||||||
chr3:47930877 | G | A | 1 | a0002c0002t0005g0028 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.293-2527C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47930877 | |||||||
chr3:47930885 | C | A | 1 | a0002c0002t0005g0040 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.293-2535G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47930885 | |||||||
chr3:47931595 | C | T | 1 | a0018c0016t0005g0031 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.293-3245G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47931595 | |||||||
chr3:47931596 | G | A | 10 | a0004c0004t0002g0083 a0004c0004t0002g0084 a0004c0004t0002g0085 others(7): Show |
10 | HG01934.hp1 HG02040.hp2 HG02071.hp2 others(7): Show |
intron_variant | MODIFIER | c.293-3246C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47931596 | |||||||
chr3:47931656 | A | AT | 81 | a0001c0001t0001g0129 a0001c0001t0001g0196 a0001c0001t0022g0213 others(78): Show |
82 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.293-3307dupA | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47931656 | |||||||
chr3:47931656 | A | ATT | 8 | a0001c0001t0001g0197 a0002c0002t0002g0055 a0002c0002t0002g0061 others(5): Show |
8 | HG01109.hp1 HG01169.hp2 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.293-3308_293-3307d others(4): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47931656 | |||||||
chr3:47931656 | A | T | 1 | a0002c0002t0002g0094 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.293-3306T>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47931656 | |||||||
chr3:47931705 | A | G | 1 | a0021c0028t0002g0224 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.293-3355T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47931705 | |||||||
chr3:47932124 | T | A | 8 | a0002c0002t0002g0045 a0002c0002t0002g0055 a0002c0002t0002g0056 others(5): Show |
8 | HG02559.hp1 HG02572.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.293-3774A>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47932124 | |||||||
chr3:47932260 | A | G | 1 | a0001c0007t0001g0219 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.293-3910T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47932260 | |||||||
chr3:47933002 | A | C | 1 | a0001c0001t0001g0158 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.293-4652T>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47933002 | |||||||
chr3:47933299 | G | C | 1 | a0001c0001t0009g0205 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.293-4949C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47933299 | |||||||
chr3:47933450 | T | C | 1 | a0002c0002t0002g0089 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.293-5100A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47933450 | |||||||
chr3:47933601 | C | CT | 106 | a0001c0001t0001g0129 a0001c0001t0001g0206 a0001c0001t0001g0210 others(103): Show |
107 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.293-5252dupA | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47933601 | |||||||
chr3:47933601 | C | CTT | 18 | a0002c0002t0002g0018 a0002c0002t0002g0020 a0002c0002t0002g0022 others(15): Show |
18 | HG00673.hp2 HG00738.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.293-5253_293-5252d others(4): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47933601 | |||||||
chr3:47933701 | C | A | 1 | a0001c0007t0001g0220 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.293-5351G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47933701 | |||||||
chr3:47933757 | C | T | 124 | a0002c0002t0002g0001 a0002c0002t0002g0004 a0002c0002t0002g0005 others(121): Show |
125 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.293-5407G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47933757 | |||||||
chr3:47934138 | G | C | 3 | a0009c0009t0002g0046 a0009c0009t0002g0047 a0009c0009t0002g0048 |
3 | HG01891.hp2 HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.293-5788C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47934138 | |||||||
chr3:47934417 | C | T | 2 | a0002c0002t0002g0020 a0015c0021t0002g0011 |
2 | HG00597.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.293-6067G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47934417 | |||||||
chr3:47934655 | C | T | 1 | a0001c0001t0001g0203 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.293-6305G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47934655 | |||||||
chr3:47934714 | T | C | 1 | a0016c0027t0001g0175 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.293-6364A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47934714 | |||||||
chr3:47934910 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.293-6560G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47934910 | |||||||
chr3:47934912 | T | C | 29 | a0003c0003t0003g0095 a0003c0003t0003g0098 a0003c0003t0003g0099 others(26): Show |
29 | HG00738.hp1 HG01109.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.293-6562A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47934912 | |||||||
chr3:47934949 | C | T | 3 | a0001c0001t0001g0129 a0001c0001t0001g0153 a0001c0001t0002g0150 |
3 | HG01981.hp1 HG02135.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.293-6599G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47934949 | |||||||
chr3:47935321 | C | T | 1 | a0006c0006t0002g0081 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.293-6971G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47935321 | |||||||
chr3:47935524 | T | C | 15 | a0003c0003t0003g0095 a0003c0003t0003g0098 a0003c0003t0003g0099 others(12): Show |
15 | HG01109.hp2 HG02055.hp2 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.293-7174A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47935524 | |||||||
chr3:47935792 | C | G | 1 | a0001c0001t0001g0208 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.293-7442G>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47935792 | |||||||
chr3:47935808 | G | A | 2 | a0002c0002t0002g0037 a0002c0002t0002g0039 |
2 | HG02135.hp1 NA18946.hp1 |
intron_variant | MODIFIER | c.293-7458C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47935808 | |||||||
chr3:47935844 | C | A | 2 | a0010c0013t0010g0222 a0021c0028t0002g0224 |
2 | HG02145.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.293-7494G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47935844 | |||||||
chr3:47935875 | G | A | 1 | a0008c0010t0007g0112 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.293-7525C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47935875 | |||||||
chr3:47935939 | C | CA | 7 | a0001c0001t0001g0145 a0001c0001t0001g0172 a0001c0001t0001g0208 others(4): Show |
7 | HG00609.hp2 HG00733.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.293-7590dupT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47935939 | |||||||
chr3:47935939 | CA | C | 6 | a0001c0001t0001g0138 a0001c0001t0001g0140 a0002c0002t0002g0091 others(3): Show |
6 | HG01891.hp2 HG02015.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.293-7590delT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47935939 | |||||||
chr3:47935956 | A | T | 31 | a0002c0002t0002g0004 a0002c0002t0002g0005 a0002c0002t0002g0010 others(28): Show |
31 | HG00099.hp2 HG00597.hp2 HG00673.hp2 others(28): Show |
intron_variant | MODIFIER | c.293-7606T>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47935956 | |||||||
chr3:47935957 | AT | A | 10 | a0005c0005t0003g0114 a0005c0005t0003g0115 a0005c0005t0003g0116 others(7): Show |
10 | HG00738.hp1 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.293-7608delA | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47935957 | |||||||
chr3:47936479 | G | A | 1 | a0010c0013t0010g0222 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.293-8129C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47936479 | |||||||
chr3:47936699 | G | A | 7 | a0002c0002t0002g0027 a0002c0002t0002g0029 a0002c0002t0002g0030 others(4): Show |
7 | HG00544.hp2 HG02735.hp1 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.293-8349C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47936699 | |||||||
chr3:47936809 | C | T | 1 | a0002c0002t0002g0063 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.293-8459G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47936809 | |||||||
chr3:47936921 | A | G | 1 | a0002c0002t0013g0065 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.293-8571T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47936921 | |||||||
chr3:47936980 | CA | C | 122 | a0001c0001t0001g0163 a0001c0001t0001g0171 a0002c0002t0002g0001 others(119): Show |
123 | HG00099.hp2 HG00544.hp2 HG00597.hp2 others(120): Show |
intron_variant | MODIFIER | c.293-8631delT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47936980 | |||||||
chr3:47937583 | T | A | 2 | a0008c0010t0007g0111 a0008c0010t0007g0112 |
2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.293-9233A>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47937583 | |||||||
chr3:47937618 | T | C | 2 | a0001c0001t0001g0126 a0001c0001t0001g0201 |
2 | HG00609.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.293-9268A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47937618 | |||||||
chr3:47937656 | C | CT | 10 | a0001c0001t0001g0185 a0001c0001t0001g0200 a0001c0001t0001g0210 others(7): Show |
10 | HG00673.hp1 HG01257.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.293-9307dupA | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47937656 | |||||||
chr3:47937656 | CT | C | 25 | a0001c0001t0001g0179 a0002c0002t0002g0030 a0003c0003t0003g0095 others(22): Show |
25 | HG01109.hp2 HG01934.hp1 HG02040.hp2 others(22): Show |
intron_variant | MODIFIER | c.293-9307delA | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47937656 | |||||||
chr3:47937656 | CTT | C | 94 | a0002c0002t0002g0001 a0002c0002t0002g0004 a0002c0002t0002g0005 others(91): Show |
95 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.293-9308_293-9307d others(4): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47937656 | |||||||
chr3:47937656 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0137 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.293-9316_293-9307d others(12): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47937656 | |||||||
chr3:47937669 | T | G | 1 | a0001c0001t0001g0137 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.293-9319A>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47937669 | |||||||
chr3:47937745 | T | A | 6 | a0004c0004t0002g0083 a0004c0004t0002g0084 a0004c0004t0002g0085 others(3): Show |
6 | HG02040.hp2 HG02071.hp2 HG02083.hp2 others(3): Show |
intron_variant | MODIFIER | c.293-9395A>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47937745 | |||||||
chr3:47937749 | C | T | 1 | a0010c0013t0010g0222 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.293-9399G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47937749 | |||||||
chr3:47937806 | C | T | 1 | a0010c0013t0010g0002 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.293-9456G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47937806 | |||||||
chr3:47938040 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.293-9690G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47938040 | |||||||
chr3:47938119 | C | T | 1 | a0001c0001t0001g0183 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.293-9769G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47938119 | |||||||
chr3:47938452 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.293-10102G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47938452 | |||||||
chr3:47938461 | C | A | 1 | a0010c0013t0010g0002 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.293-10111G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47938461 | |||||||
chr3:47938601 | G | A | 1 | a0001c0001t0001g0199 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.293-10251C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47938601 | |||||||
chr3:47938685 | A | G | 29 | a0003c0003t0003g0095 a0003c0003t0003g0098 a0003c0003t0003g0099 others(26): Show |
29 | HG00738.hp1 HG01109.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.293-10335T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47938685 | |||||||
chr3:47938816 | A | G | 124 | a0002c0002t0002g0001 a0002c0002t0002g0004 a0002c0002t0002g0005 others(121): Show |
125 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.293-10466T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47938816 | |||||||
chr3:47938992 | T | C | 1 | a0001c0001t0001g0194 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.293-10642A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47938992 | |||||||
chr3:47939048 | T | A | 1 | a0002c0002t0002g0057 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.293-10698A>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47939048 | |||||||
chr3:47939166 | C | T | 1 | a0001c0001t0001g0195 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.293-10816G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47939166 | |||||||
chr3:47939325 | TTTCA | T | 26 | a0003c0003t0003g0095 a0003c0003t0003g0098 a0003c0003t0003g0099 others(23): Show |
26 | HG00738.hp1 HG01109.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.293-10979_293-1097 others(8): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47939325 | |||||||
chr3:47939341 | G | A | 1 | a0022c0030t0023g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.293-10991C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47939341 | |||||||
chr3:47939405 | C | T | 2 | a0002c0002t0002g0069 a0002c0002t0002g0231 |
2 | HG00741.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.293-11055G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47939405 | |||||||
chr3:47939499 | A | C | 1 | a0022c0030t0023g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.293-11149T>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47939499 | |||||||
chr3:47939589 | T | A | 1 | a0002c0002t0002g0089 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.293-11239A>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47939589 | |||||||
chr3:47939590 | A | T | 1 | a0010c0013t0010g0002 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.293-11240T>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47939590 | |||||||
chr3:47939684 | C | G | 1 | a0010c0013t0010g0222 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.293-11334G>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47939684 | |||||||
chr3:47939709 | GT | G | 127 | a0001c0001t0001g0158 a0001c0001t0001g0168 a0001c0001t0001g0169 others(124): Show |
128 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(125): Show |
intron_variant | MODIFIER | c.293-11360delA | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47939709 | |||||||
chr3:47939736 | C | T | 1 | a0022c0030t0023g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.293-11386G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47939736 | |||||||
chr3:47939784 | C | G | 1 | a0001c0001t0001g0140 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.293-11434G>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47939784 | |||||||
chr3:47939867 | G | A | 1 | a0002c0002t0002g0032 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.293-11517C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47939867 | |||||||
chr3:47940068 | C | A | 1 | a0001c0007t0001g0221 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.293-11718G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47940068 | |||||||
chr3:47940407 | A | T | 1 | a0001c0001t0001g0139 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.293-12057T>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47940407 | |||||||
chr3:47940475 | T | C | 2 | a0010c0013t0010g0222 a0021c0028t0002g0224 |
2 | HG02145.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.293-12125A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47940475 | |||||||
chr3:47941220 | C | CA | 14 | a0001c0001t0001g0042 a0001c0001t0001g0128 a0001c0001t0001g0153 others(11): Show |
14 | HG01074.hp1 HG01257.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.293-12871dupT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47941220 | |||||||
chr3:47941220 | CAA | C | 10 | a0002c0002t0002g0090 a0003c0003t0003g0107 a0003c0003t0003g0108 others(7): Show |
10 | HG02055.hp2 HG02145.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.293-12872_293-1287 others(6): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47941220 | |||||||
chr3:47941220 | CAAA | C | 37 | a0002c0002t0002g0089 a0002c0002t0005g0026 a0002c0002t0005g0040 others(34): Show |
37 | HG00738.hp1 HG01074.hp2 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.293-12873_293-1287 others(7): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47941220 | |||||||
chr3:47941220 | CAAAA | C | 76 | a0002c0002t0002g0001 a0002c0002t0002g0004 a0002c0002t0002g0005 others(73): Show |
77 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.293-12874_293-1287 others(8): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47941220 | |||||||
chr3:47941627 | C | CA | 7 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(4): Show |
7 | HG01074.hp1 HG01169.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.293-13278dupT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47941627 | |||||||
chr3:47941627 | C | CAA | 8 | a0005c0005t0003g0114 a0005c0005t0003g0115 a0005c0005t0003g0117 others(5): Show |
8 | HG00738.hp1 HG01884.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.293-13279_293-1327 others(6): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47941627 | |||||||
chr3:47941632 | A | C | 2 | a0002c0002t0002g0069 a0002c0002t0002g0231 |
2 | HG00741.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.293-13282T>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47941632 | |||||||
chr3:47941633 | A | C | 21 | a0003c0003t0003g0101 a0003c0003t0003g0102 a0003c0003t0003g0103 others(18): Show |
21 | HG01934.hp1 HG02040.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.293-13283T>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47941633 | |||||||
chr3:47941637 | A | AAAAACTG others(17): Show |
1 | a0002c0002t0002g0037 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.293-13311_293-1328 others(28): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47941637 | |||||||
chr3:47941701 | T | C | 1 | a0004c0004t0020g0080 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.293-13351A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47941701 | |||||||
chr3:47941748 | TTGCACTC others(5): Show |
T | 6 | a0004c0004t0002g0083 a0004c0004t0002g0084 a0004c0004t0002g0085 others(3): Show |
6 | HG02040.hp2 HG02071.hp2 HG02083.hp2 others(3): Show |
intron_variant | MODIFIER | c.293-13410_293-1339 others(16): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47941748 | |||||||
chr3:47941762 | G | A | 6 | a0004c0004t0002g0083 a0004c0004t0002g0084 a0004c0004t0002g0085 others(3): Show |
6 | HG02040.hp2 HG02071.hp2 HG02083.hp2 others(3): Show |
intron_variant | MODIFIER | c.293-13412C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47941762 | |||||||
chr3:47941786 | C | CA | 11 | a0001c0001t0001g0129 a0001c0001t0001g0134 a0001c0001t0001g0180 others(8): Show |
11 | HG00639.hp2 HG02071.hp1 HG02135.hp2 others(8): Show |
intron_variant | MODIFIER | c.293-13437dupT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47941786 | |||||||
chr3:47941858 | T | G | 1 | a0022c0030t0023g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.293-13508A>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47941858 | |||||||
chr3:47942543 | A | G | 15 | a0003c0003t0003g0095 a0003c0003t0003g0098 a0003c0003t0003g0099 others(12): Show |
15 | HG01109.hp2 HG02055.hp2 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.293-14193T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47942543 | |||||||
chr3:47942696 | G | A | 1 | a0022c0030t0023g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.293-14346C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47942696 | |||||||
chr3:47942937 | C | T | 1 | a0004c0004t0018g0060 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.293-14587G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47942937 | |||||||
chr3:47943263 | G | A | 1 | a0028c0017t0002g0038 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.293-14913C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47943263 | |||||||
chr3:47943334 | A | G | 124 | a0002c0002t0002g0001 a0002c0002t0002g0004 a0002c0002t0002g0005 others(121): Show |
125 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.293-14984T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47943334 | |||||||
chr3:47943566 | G | A | 1 | a0010c0013t0010g0222 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.293-15216C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47943566 | |||||||
chr3:47943598 | A | G | 1 | a0007c0008t0006g0226 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.293-15248T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47943598 | |||||||
chr3:47943871 | C | T | 124 | a0002c0002t0002g0001 a0002c0002t0002g0004 a0002c0002t0002g0005 others(121): Show |
125 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.293-15521G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47943871 | |||||||
chr3:47944215 | C | T | 3 | a0009c0009t0002g0046 a0009c0009t0002g0047 a0009c0009t0002g0048 |
3 | HG01891.hp2 HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.293-15865G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47944215 | |||||||
chr3:47944242 | G | A | 90 | a0002c0002t0002g0001 a0002c0002t0002g0004 a0002c0002t0002g0005 others(87): Show |
91 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.293-15892C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47944242 | |||||||
chr3:47944661 | T | G | 1 | a0002c0002t0002g0045 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.293-16311A>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47944661 | |||||||
chr3:47944902 | C | T | 80 | a0002c0002t0002g0001 a0002c0002t0002g0004 a0002c0002t0002g0005 others(77): Show |
81 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.293-16552G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47944902 | |||||||
chr3:47944949 | C | CT | 15 | a0001c0001t0001g0160 a0001c0001t0001g0188 a0001c0001t0001g0192 others(12): Show |
16 | HG00741.hp1 HG01099.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.293-16600dupA | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47944949 | |||||||
chr3:47944949 | CT | C | 8 | a0001c0001t0001g0162 a0001c0001t0001g0187 a0001c0001t0001g0195 others(5): Show |
8 | HG01891.hp1 HG02273.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.293-16600delA | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47944949 | |||||||
chr3:47945077 | G | T | 6 | a0004c0004t0002g0083 a0004c0004t0002g0084 a0004c0004t0002g0085 others(3): Show |
6 | HG02040.hp2 HG02071.hp2 HG02083.hp2 others(3): Show |
intron_variant | MODIFIER | c.293-16727C>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47945077 | |||||||
chr3:47945182 | T | C | 1 | a0004c0004t0020g0080 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.293-16832A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47945182 | |||||||
chr3:47945245 | G | A | 3 | a0009c0009t0002g0046 a0009c0009t0002g0047 a0009c0009t0002g0048 |
3 | HG01891.hp2 HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.293-16895C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47945245 | |||||||
chr3:47945975 | C | T | 1 | a0022c0030t0023g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.293-17625G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47945975 | |||||||
chr3:47946117 | G | T | 1 | a0001c0001t0001g0147 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.293-17767C>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47946117 | |||||||
chr3:47946214 | A | T | 1 | a0001c0001t0001g0151 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.293-17864T>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47946214 | |||||||
chr3:47946228 | C | T | 8 | a0002c0002t0002g0045 a0002c0002t0002g0055 a0002c0002t0002g0056 others(5): Show |
8 | HG02559.hp1 HG02572.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.293-17878G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47946228 | |||||||
chr3:47946238 | C | T | 1 | a0022c0030t0023g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.293-17888G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47946238 | |||||||
chr3:47946654 | C | CA | 78 | a0001c0001t0001g0147 a0001c0001t0001g0156 a0001c0001t0001g0164 others(75): Show |
79 | HG00280.hp2 HG00544.hp2 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.293-18305dupT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47946654 | |||||||
chr3:47946654 | C | CAA | 33 | a0002c0002t0002g0004 a0002c0002t0002g0005 a0002c0002t0002g0010 others(30): Show |
33 | HG00099.hp2 HG00597.hp2 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.293-18306_293-1830 others(6): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47946654 | |||||||
chr3:47946654 | C | CAAA | 8 | a0002c0002t0002g0018 a0002c0002t0002g0020 a0004c0004t0002g0085 others(5): Show |
8 | HG01891.hp2 HG01934.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.293-18307_293-1830 others(7): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47946654 | |||||||
chr3:47946654 | CAAAAAAA others(6): Show |
C | 1 | a0023c0022t0002g0088 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.293-18317_293-1830 others(17): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47946654 | |||||||
chr3:47947126 | T | C | 1 | a0002c0002t0002g0056 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.293-18776A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47947126 | |||||||
chr3:47947190 | T | C | 1 | a0001c0007t0001g0219 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.293-18840A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47947190 | |||||||
chr3:47947420 | C | T | 1 | a0002c0002t0002g0052 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.293-19070G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47947420 | |||||||
chr3:47947704 | G | A | 2 | a0002c0002t0002g0013 a0002c0002t0002g0014 |
2 | NA19004.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.293-19354C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47947704 | |||||||
chr3:47947804 | C | CA | 6 | a0001c0001t0001g0173 a0001c0001t0001g0176 a0001c0001t0022g0213 others(3): Show |
6 | HG02486.hp1 HG02717.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.293-19455dupT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47947804 | |||||||
chr3:47948195 | C | T | 1 | a0002c0002t0005g0028 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.293-19845G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47948195 | |||||||
chr3:47948225 | C | CT | 9 | a0001c0001t0001g0214 a0001c0001t0001g0216 a0002c0002t0005g0026 others(6): Show |
9 | HG01123.hp2 HG02602.hp1 HG02698.hp2 others(6): Show |
intron_variant | MODIFIER | c.293-19876dupA | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47948225 | |||||||
chr3:47948256 | A | G | 3 | a0009c0009t0002g0046 a0009c0009t0002g0047 a0009c0009t0002g0048 |
3 | HG01891.hp2 HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.293-19906T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47948256 | |||||||
chr3:47948463 | A | G | 2 | a0001c0001t0001g0162 a0001c0001t0001g0163 |
2 | NA18940.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.293-20113T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47948463 | |||||||
chr3:47948504 | G | A | 1 | a0002c0020t0002g0054 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.293-20154C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47948504 | |||||||
chr3:47948951 | G | A | 1 | a0001c0001t0001g0154 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.293-20601C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47948951 | |||||||
chr3:47949010 | G | C | 33 | a0002c0002t0002g0001 a0002c0002t0002g0052 a0002c0002t0002g0061 others(30): Show |
34 | HG00280.hp2 HG00639.hp1 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.293-20660C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47949010 | |||||||
chr3:47949194 | G | A | 3 | a0010c0013t0010g0002 a0010c0013t0010g0222 a0021c0028t0002g0224 |
3 | HG02145.hp2 HG02451.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.293-20844C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47949194 | |||||||
chr3:47949465 | C | CA | 20 | a0001c0001t0001g0147 a0001c0001t0001g0162 a0001c0001t0001g0180 others(17): Show |
20 | HG00673.hp1 HG00738.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.293-21116dupT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47949465 | |||||||
chr3:47949465 | CA | C | 83 | a0001c0001t0001g0168 a0001c0001t0001g0202 a0001c0001t0022g0213 others(80): Show |
84 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.293-21116delT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47949465 | |||||||
chr3:47949466 | A | C | 1 | a0004c0004t0002g0085 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.293-21116T>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47949466 | |||||||
chr3:47949467 | A | C | 2 | a0004c0004t0002g0083 a0020c0023t0002g0053 |
2 | HG02071.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.293-21117T>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47949467 | |||||||
chr3:47949844 | C | T | 9 | a0002c0002t0002g0045 a0002c0002t0002g0055 a0002c0002t0002g0056 others(6): Show |
9 | HG02559.hp1 HG02572.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.293-21494G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47949844 | |||||||
chr3:47949889 | CA | C | 124 | a0002c0002t0002g0001 a0002c0002t0002g0004 a0002c0002t0002g0005 others(121): Show |
125 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.293-21540delT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47949889 | |||||||
chr3:47949905 | G | C | 1 | a0015c0021t0002g0011 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.293-21555C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47949905 | |||||||
chr3:47949970 | T | C | 2 | a0007c0008t0006g0131 a0007c0008t0006g0226 |
2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.293-21620A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47949970 | |||||||
chr3:47950442 | C | T | 1 | a0005c0005t0003g0121 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.293-22092G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47950442 | |||||||
chr3:47950698 | T | C | 1 | a0001c0001t0001g0132 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.293-22348A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47950698 | |||||||
chr3:47951204 | T | G | 3 | a0010c0013t0010g0002 a0010c0013t0010g0222 a0021c0028t0002g0224 |
3 | HG02145.hp2 HG02451.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.293-22854A>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47951204 | |||||||
chr3:47951496 | C | T | 1 | a0001c0001t0001g0184 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.293-23146G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47951496 | |||||||
chr3:47951659 | T | A | 1 | a0005c0005t0003g0114 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.293-23309A>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47951659 | |||||||
chr3:47951659 | T | G | 118 | a0002c0002t0002g0001 a0002c0002t0002g0004 a0002c0002t0002g0005 others(115): Show |
119 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.293-23309A>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47951659 | |||||||
chr3:47951793 | G | A | 15 | a0003c0003t0003g0095 a0003c0003t0003g0098 a0003c0003t0003g0099 others(12): Show |
15 | HG01109.hp2 HG02055.hp2 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.293-23443C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47951793 | |||||||
chr3:47951919 | G | C | 1 | a0016c0027t0001g0175 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.293-23569C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47951919 | |||||||
chr3:47951943 | T | A | 124 | a0002c0002t0002g0001 a0002c0002t0002g0004 a0002c0002t0002g0005 others(121): Show |
125 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.293-23593A>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47951943 | |||||||
chr3:47952040 | C | A | 1 | a0001c0001t0001g0179 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.293-23690G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47952040 | |||||||
chr3:47952065 | G | A | 2 | a0004c0004t0011g0049 a0004c0004t0011g0050 |
2 | HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.293-23715C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47952065 | |||||||
chr3:47952118 | T | C | 1 | a0005c0005t0003g0122 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.293-23768A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47952118 | |||||||
chr3:47952228 | A | G | 172 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(169): Show |
173 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(170): Show |
intron_variant | MODIFIER | c.293-23878T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47952228 | |||||||
chr3:47952265 | G | A | 1 | a0002c0002t0002g0024 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.293-23915C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47952265 | |||||||
chr3:47952384 | G | T | 4 | a0002c0002t0005g0026 a0002c0002t0005g0028 a0002c0002t0005g0040 others(1): Show |
4 | HG01074.hp2 HG01346.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.293-24034C>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47952384 | |||||||
chr3:47952482 | G | T | 1 | a0009c0009t0002g0048 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.293-24132C>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47952482 | |||||||
chr3:47952645 | T | A | 2 | a0010c0013t0010g0222 a0021c0028t0002g0224 |
2 | HG02145.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.293-24295A>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47952645 | |||||||
chr3:47952654 | A | T | 2 | a0004c0004t0017g0086 a0005c0005t0003g0115 |
2 | HG02280.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.293-24304T>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47952654 | |||||||
chr3:47952659 | A | T | 8 | a0006c0006t0002g0062 a0006c0006t0002g0074 a0006c0006t0002g0075 others(5): Show |
8 | HG01123.hp2 HG02602.hp1 HG02698.hp2 others(5): Show |
intron_variant | MODIFIER | c.293-24309T>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47952659 | |||||||
chr3:47952663 | A | AAAAATAA others(4): Show |
1 | a0022c0030t0023g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.293-24314_293-2431 others(15): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47952663 | |||||||
chr3:47952663 | AAAAAATA others(5): Show |
A | 1 | a0020c0023t0002g0053 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.293-24325_293-2431 others(16): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47952663 | |||||||
chr3:47952905 | C | T | 1 | a0002c0002t0002g0036 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.293-24555G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47952905 | |||||||
chr3:47952941 | C | CA | 8 | a0001c0001t0001g0132 a0002c0002t0002g0027 a0002c0002t0002g0029 others(5): Show |
8 | HG00544.hp2 HG02735.hp1 NA18940.hp1 others(5): Show |
intron_variant | MODIFIER | c.293-24592dupT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47952941 | |||||||
chr3:47953021 | G | C | 1 | a0023c0022t0002g0088 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.293-24671C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47953021 | |||||||
chr3:47953462 | C | T | 1 | a0004c0004t0017g0086 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.292+24403G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47953462 | |||||||
chr3:47953678 | A | C | 121 | a0001c0001t0001g0067 a0002c0002t0002g0001 a0002c0002t0002g0004 others(118): Show |
122 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.292+24187T>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47953678 | |||||||
chr3:47953734 | G | GC | 125 | a0001c0001t0001g0067 a0002c0002t0002g0001 a0002c0002t0002g0004 others(122): Show |
126 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.292+24130_292+2413 others(5): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47953734 | |||||||
chr3:47954046 | A | C | 1 | a0001c0001t0001g0200 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.292+23819T>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47954046 | |||||||
chr3:47954555 | T | A | 6 | a0004c0004t0002g0083 a0004c0004t0002g0084 a0004c0004t0002g0085 others(3): Show |
6 | HG02040.hp2 HG02071.hp2 HG02083.hp2 others(3): Show |
intron_variant | MODIFIER | c.292+23310A>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47954555 | |||||||
chr3:47954925 | T | C | 1 | a0001c0001t0009g0178 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.292+22940A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47954925 | |||||||
chr3:47955218 | A | G | 1 | a0028c0017t0002g0038 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.292+22647T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47955218 | |||||||
chr3:47955282 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.292+22583G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47955282 | |||||||
chr3:47955435 | T | TAC | 8 | a0001c0001t0001g0129 a0001c0001t0002g0150 a0001c0001t0016g0135 others(5): Show |
8 | HG02071.hp2 HG02135.hp2 HG02273.hp2 others(5): Show |
intron_variant | MODIFIER | c.292+22428_292+2242 others(6): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47955435 | |||||||
chr3:47955435 | T | TACAC | 7 | a0005c0005t0003g0114 a0005c0005t0003g0115 a0005c0005t0003g0117 others(4): Show |
7 | HG01884.hp1 HG01891.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.292+22426_292+2242 others(8): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47955435 | |||||||
chr3:47955435 | TAC | T | 84 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0126 others(81): Show |
84 | HG00099.hp1 HG00280.hp1 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.292+22428_292+2242 others(6): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47955435 | |||||||
chr3:47955435 | TACAC | T | 42 | a0001c0001t0001g0041 a0001c0001t0001g0067 a0001c0001t0001g0128 others(39): Show |
42 | HG00099.hp2 HG00544.hp1 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.292+22426_292+2242 others(8): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47955435 | |||||||
chr3:47955435 | TACACAC | T | 41 | a0002c0002t0002g0001 a0002c0002t0002g0027 a0002c0002t0002g0029 others(38): Show |
42 | HG00280.hp2 HG00544.hp2 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.292+22424_292+2242 others(10): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47955435 | |||||||
chr3:47955435 | TACACACA others(1): Show |
T | 8 | a0002c0002t0002g0030 a0002c0002t0002g0034 a0002c0002t0002g0035 others(5): Show |
8 | HG01981.hp2 HG03041.hp2 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.292+22422_292+2242 others(12): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47955435 | |||||||
chr3:47955435 | TACACACA others(3): Show |
T | 2 | a0002c0002t0002g0072 a0026c0019t0002g0077 |
2 | HG04204.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.292+22420_292+2242 others(14): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47955435 | |||||||
chr3:47955435 | TACACACA others(9): Show |
T | 3 | a0001c0001t0008g0166 a0001c0001t0008g0167 a0002c0002t0002g0082 |
3 | HG02258.hp2 HG03471.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.292+22414_292+2242 others(20): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47955435 | |||||||
chr3:47955437 | C | CGT | 2 | a0003c0003t0003g0095 a0003c0003t0003g0100 |
2 | HG01109.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.292+22427_292+2242 others(6): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47955437 | |||||||
chr3:47955438 | A | G | 14 | a0003c0003t0003g0098 a0003c0003t0003g0099 a0003c0003t0003g0101 others(11): Show |
14 | HG02055.hp2 HG02630.hp1 HG02717.hp2 others(11): Show |
intron_variant | MODIFIER | c.292+22427T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47955438 | |||||||
chr3:47955439 | C | T | 14 | a0003c0003t0003g0098 a0003c0003t0003g0099 a0003c0003t0003g0101 others(11): Show |
14 | HG02055.hp2 HG02630.hp1 HG02717.hp2 others(11): Show |
intron_variant | MODIFIER | c.292+22426G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47955439 | |||||||
chr3:47955548 | C | T | 6 | a0004c0004t0002g0083 a0004c0004t0002g0084 a0004c0004t0002g0085 others(3): Show |
6 | HG02040.hp2 HG02071.hp2 HG02083.hp2 others(3): Show |
intron_variant | MODIFIER | c.292+22317G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47955548 | |||||||
chr3:47955942 | G | A | 3 | a0008c0010t0007g0111 a0008c0010t0007g0112 a0008c0010t0007g0113 |
3 | HG00738.hp1 HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.292+21923C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47955942 | |||||||
chr3:47955999 | C | T | 1 | a0005c0005t0003g0116 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.292+21866G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47955999 | |||||||
chr3:47956336 | CAA | C | 90 | a0002c0002t0002g0001 a0002c0002t0002g0004 a0002c0002t0002g0005 others(87): Show |
91 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.292+21527_292+2152 others(6): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47956336 | |||||||
chr3:47956474 | G | C | 1 | a0023c0022t0002g0088 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.292+21391C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47956474 | |||||||
chr3:47956665 | T | C | 1 | a0010c0013t0010g0222 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.292+21200A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47956665 | |||||||
chr3:47956799 | A | T | 1 | a0002c0002t0002g0036 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.292+21066T>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47956799 | |||||||
chr3:47957087 | TATA | T | 3 | a0010c0013t0010g0002 a0010c0013t0010g0222 a0021c0028t0002g0224 |
3 | HG02145.hp2 HG02451.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.292+20775_292+2077 others(7): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47957087 | |||||||
chr3:47957177 | T | G | 2 | a0003c0003t0003g0106 a0026c0019t0002g0077 |
2 | HG03579.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.292+20688A>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47957177 | |||||||
chr3:47957288 | C | T | 3 | a0010c0013t0010g0002 a0010c0013t0010g0222 a0021c0028t0002g0224 |
3 | HG02145.hp2 HG02451.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.292+20577G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47957288 | |||||||
chr3:47957418 | G | A | 4 | a0001c0001t0001g0214 a0001c0001t0001g0216 a0001c0001t0022g0213 others(1): Show |
4 | HG00544.hp1 NA18982.hp1 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.292+20447C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47957418 | |||||||
chr3:47957476 | A | G | 121 | a0001c0001t0001g0067 a0002c0002t0002g0001 a0002c0002t0002g0004 others(118): Show |
122 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.292+20389T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47957476 | |||||||
chr3:47957750 | T | G | 7 | a0002c0002t0002g0027 a0002c0002t0002g0029 a0002c0002t0002g0030 others(4): Show |
7 | HG00544.hp2 HG02735.hp1 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.292+20115A>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47957750 | |||||||
chr3:47957823 | C | T | 4 | a0007c0008t0006g0131 a0007c0008t0006g0149 a0007c0008t0006g0152 others(1): Show |
4 | HG01891.hp1 HG02970.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.292+20042G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47957823 | |||||||
chr3:47957847 | T | A | 125 | a0001c0001t0001g0067 a0002c0002t0002g0001 a0002c0002t0002g0004 others(122): Show |
126 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.292+20018A>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47957847 | |||||||
chr3:47958184 | A | G | 125 | a0001c0001t0001g0067 a0002c0002t0002g0001 a0002c0002t0002g0004 others(122): Show |
126 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.292+19681T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47958184 | |||||||
chr3:47958293 | T | C | 23 | a0002c0002t0002g0004 a0002c0002t0002g0005 a0002c0002t0002g0010 others(20): Show |
23 | HG00099.hp2 HG00597.hp2 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.292+19572A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47958293 | |||||||
chr3:47958316 | C | T | 1 | a0010c0013t0010g0002 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.292+19549G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47958316 | |||||||
chr3:47958498 | A | G | 4 | a0001c0007t0001g0218 a0001c0007t0001g0219 a0001c0007t0001g0220 others(1): Show |
4 | HG02451.hp1 HG02572.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.292+19367T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47958498 | |||||||
chr3:47958629 | G | C | 23 | a0002c0002t0002g0004 a0002c0002t0002g0005 a0002c0002t0002g0010 others(20): Show |
23 | HG00099.hp2 HG00597.hp2 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.292+19236C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47958629 | |||||||
chr3:47958631 | C | T | 1 | a0010c0013t0010g0002 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.292+19234G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47958631 | |||||||
chr3:47958682 | A | AT | 12 | a0001c0001t0001g0147 a0001c0001t0001g0157 a0001c0001t0001g0160 others(9): Show |
12 | HG00597.hp1 HG00741.hp1 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.292+19182dupA | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47958682 | |||||||
chr3:47958682 | AT | A | 77 | a0001c0001t0001g0067 a0001c0001t0001g0180 a0001c0001t0001g0216 others(74): Show |
78 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.292+19182delA | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47958682 | |||||||
chr3:47958872 | C | T | 1 | a0004c0004t0002g0223 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.292+18993G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47958872 | |||||||
chr3:47958873 | G | A | 7 | a0002c0002t0002g0027 a0002c0002t0002g0029 a0002c0002t0002g0030 others(4): Show |
7 | HG00544.hp2 HG02735.hp1 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.292+18992C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47958873 | |||||||
chr3:47959059 | A | G | 1 | a0002c0002t0002g0035 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.292+18806T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47959059 | |||||||
chr3:47959264 | C | T | 1 | a0010c0013t0010g0222 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.292+18601G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47959264 | |||||||
chr3:47959301 | T | C | 3 | a0009c0009t0002g0046 a0009c0009t0002g0047 a0009c0009t0002g0048 |
3 | HG01891.hp2 HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.292+18564A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47959301 | |||||||
chr3:47959319 | G | A | 1 | a0006c0006t0002g0079 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.292+18546C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47959319 | |||||||
chr3:47959458 | G | GA | 7 | a0001c0001t0001g0173 a0001c0001t0001g0177 a0002c0002t0002g0005 others(4): Show |
7 | HG03579.hp2 NA18956.hp2 NA18967.hp2 others(4): Show |
intron_variant | MODIFIER | c.292+18406dupT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47959458 | |||||||
chr3:47959696 | A | T | 1 | a0001c0001t0001g0042 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.292+18169T>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47959696 | |||||||
chr3:47959758 | C | CA | 7 | a0001c0001t0001g0171 a0001c0001t0001g0173 a0001c0001t0022g0213 others(4): Show |
7 | HG02965.hp1 HG03834.hp1 HG04115.hp2 others(4): Show |
intron_variant | MODIFIER | c.292+18106dupT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47959758 | |||||||
chr3:47959758 | CA | C | 13 | a0003c0003t0003g0095 a0003c0003t0003g0098 a0003c0003t0003g0099 others(10): Show |
13 | HG01109.hp2 HG02630.hp1 HG02922.hp1 others(10): Show |
intron_variant | MODIFIER | c.292+18106delT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47959758 | |||||||
chr3:47960458 | T | C | 1 | a0001c0001t0001g0151 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.292+17407A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47960458 | |||||||
chr3:47960733 | T | C | 1 | a0001c0001t0001g0129 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.292+17132A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47960733 | |||||||
chr3:47960735 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.292+17130C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47960735 | |||||||
chr3:47960896 | T | G | 29 | a0003c0003t0003g0095 a0003c0003t0003g0098 a0003c0003t0003g0099 others(26): Show |
29 | HG00738.hp1 HG01109.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.292+16969A>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47960896 | |||||||
chr3:47960928 | C | G | 1 | a0003c0003t0003g0100 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.292+16937G>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47960928 | |||||||
chr3:47961112 | C | G | 1 | a0001c0001t0001g0151 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.292+16753G>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47961112 | |||||||
chr3:47961150 | T | C | 121 | a0001c0001t0001g0067 a0002c0002t0002g0001 a0002c0002t0002g0004 others(118): Show |
122 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.292+16715A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47961150 | |||||||
chr3:47961487 | A | G | 16 | a0003c0003t0003g0095 a0003c0003t0003g0098 a0003c0003t0003g0099 others(13): Show |
16 | HG01109.hp2 HG02055.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.292+16378T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47961487 | |||||||
chr3:47961656 | C | A | 8 | a0002c0002t0002g0045 a0002c0002t0002g0055 a0002c0002t0002g0056 others(5): Show |
8 | HG02559.hp1 HG02572.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.292+16209G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47961656 | |||||||
chr3:47962005 | G | T | 2 | a0002c0002t0002g0030 a0002c0002t0002g0034 |
2 | NA19000.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.292+15860C>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47962005 | |||||||
chr3:47962090 | C | T | 1 | a0004c0004t0002g0085 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.292+15775G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47962090 | |||||||
chr3:47963545 | C | A | 15 | a0003c0003t0003g0095 a0003c0003t0003g0098 a0003c0003t0003g0099 others(12): Show |
15 | HG01109.hp2 HG02055.hp2 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.292+14320G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47963545 | |||||||
chr3:47963914 | T | C | 1 | a0023c0022t0002g0088 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.292+13951A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47963914 | |||||||
chr3:47964183 | A | C | 120 | a0001c0001t0001g0067 a0002c0002t0002g0001 a0002c0002t0002g0004 others(117): Show |
121 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(118): Show |
intron_variant | MODIFIER | c.292+13682T>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47964183 | |||||||
chr3:47964773 | T | C | 1 | a0001c0001t0001g0154 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.292+13092A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47964773 | |||||||
chr3:47964970 | A | C | 10 | a0005c0005t0003g0114 a0005c0005t0003g0115 a0005c0005t0003g0116 others(7): Show |
10 | HG00738.hp1 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.292+12895T>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47964970 | |||||||
chr3:47965020 | C | T | 1 | a0001c0007t0001g0221 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.292+12845G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47965020 | |||||||
chr3:47965030 | C | T | 7 | a0002c0002t0002g0027 a0002c0002t0002g0029 a0002c0002t0002g0030 others(4): Show |
7 | HG00544.hp2 HG02735.hp1 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.292+12835G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47965030 | |||||||
chr3:47965058 | T | C | 1 | a0003c0003t0003g0099 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.292+12807A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47965058 | |||||||
chr3:47965118 | G | T | 1 | a0002c0011t0002g0073 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.292+12747C>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47965118 | |||||||
chr3:47965252 | C | T | 1 | a0001c0001t0001g0203 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.292+12613G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47965252 | |||||||
chr3:47965253 | G | A | 1 | a0009c0009t0002g0048 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.292+12612C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47965253 | |||||||
chr3:47965973 | C | T | 4 | a0001c0001t0001g0067 a0002c0002t0002g0123 a0002c0011t0002g0073 others(1): Show |
4 | HG00639.hp1 HG00733.hp1 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.292+11892G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47965973 | |||||||
chr3:47965995 | T | C | 2 | a0013c0014t0001g0142 a0013c0014t0001g0143 |
2 | NA19007.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.292+11870A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47965995 | |||||||
chr3:47966043 | T | A | 1 | a0004c0004t0018g0060 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.292+11822A>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47966043 | |||||||
chr3:47966101 | C | G | 1 | a0007c0008t0006g0131 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.292+11764G>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47966101 | |||||||
chr3:47966103 | C | G | 6 | a0004c0004t0002g0083 a0004c0004t0002g0084 a0004c0004t0002g0085 others(3): Show |
6 | HG02040.hp2 HG02071.hp2 HG02083.hp2 others(3): Show |
intron_variant | MODIFIER | c.292+11762G>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47966103 | |||||||
chr3:47966150 | T | G | 1 | a0010c0013t0010g0002 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.292+11715A>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47966150 | |||||||
chr3:47966228 | C | CT | 26 | a0001c0001t0001g0043 a0001c0001t0001g0132 a0001c0001t0001g0134 others(23): Show |
26 | HG00544.hp1 HG00639.hp2 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.292+11636dupA | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47966228 | |||||||
chr3:47966228 | C | CTT | 27 | a0001c0001t0001g0128 a0001c0001t0001g0139 a0001c0001t0001g0140 others(24): Show |
27 | HG00099.hp1 HG00733.hp2 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.292+11635_292+1163 others(6): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47966228 | |||||||
chr3:47966228 | C | CTTT | 15 | a0001c0001t0001g0126 a0001c0001t0001g0129 a0001c0001t0001g0156 others(12): Show |
15 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(12): Show |
intron_variant | MODIFIER | c.292+11634_292+1163 others(7): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47966228 | |||||||
chr3:47966228 | C | CTTTT | 12 | a0001c0001t0001g0042 a0001c0001t0001g0136 a0001c0001t0001g0159 others(9): Show |
12 | HG00673.hp1 HG02451.hp1 HG02602.hp2 others(9): Show |
intron_variant | MODIFIER | c.292+11633_292+1163 others(8): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47966228 | |||||||
chr3:47966228 | CT | C | 5 | a0001c0001t0001g0041 a0001c0001t0001g0170 a0001c0001t0001g0171 others(2): Show |
5 | HG01074.hp1 HG01257.hp2 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.292+11636delA | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47966228 | |||||||
chr3:47966228 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0229 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.292+11627_292+1163 others(14): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47966228 | |||||||
chr3:47966228 | CTTTTTTT others(5): Show |
C | 4 | a0001c0007t0001g0220 a0003c0003t0021g0105 a0004c0004t0002g0085 others(1): Show |
4 | HG02071.hp2 HG02647.hp2 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.292+11625_292+1163 others(16): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47966228 | |||||||
chr3:47966228 | CTTTTTTT others(6): Show |
C | 42 | a0002c0002t0002g0013 a0002c0002t0002g0018 a0002c0002t0002g0020 others(39): Show |
42 | HG00544.hp2 HG00738.hp1 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.292+11624_292+1163 others(17): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47966228 | |||||||
chr3:47966228 | CTTTTTTT others(7): Show |
C | 73 | a0001c0001t0001g0067 a0002c0002t0002g0001 a0002c0002t0002g0004 others(70): Show |
74 | HG00099.hp2 HG00280.hp2 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.292+11623_292+1163 others(18): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47966228 | |||||||
chr3:47966228 | CTTTTTTT others(8): Show |
C | 2 | a0002c0002t0002g0052 a0002c0002t0004g0003 |
2 | HG02015.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.292+11622_292+1163 others(19): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47966228 | |||||||
chr3:47966228 | CTTTTTTT others(9): Show |
C | 1 | a0001c0001t0001g0230 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.292+11621_292+1163 others(20): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47966228 | |||||||
chr3:47966228 | CTTTTTTT others(10): Show |
C | 2 | a0022c0030t0023g0044 a0023c0022t0002g0088 |
2 | HG02486.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.292+11620_292+1163 others(21): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47966228 | |||||||
chr3:47966228 | CTTTTTTT others(12): Show |
C | 1 | a0010c0013t0010g0002 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.292+11618_292+1163 others(23): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47966228 | |||||||
chr3:47966228 | CTTTTTTT others(19): Show |
C | 1 | a0024c0029t0015g0155 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.292+11611_292+1163 others(30): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47966228 | |||||||
chr3:47966737 | C | T | 1 | a0001c0001t0001g0132 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.292+11128G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47966737 | |||||||
chr3:47967134 | T | G | 120 | a0001c0001t0001g0067 a0002c0002t0002g0001 a0002c0002t0002g0004 others(117): Show |
121 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(118): Show |
intron_variant | MODIFIER | c.292+10731A>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47967134 | |||||||
chr3:47967139 | C | T | 2 | a0004c0004t0002g0083 a0004c0004t0002g0085 |
2 | HG02083.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.292+10726G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47967139 | |||||||
chr3:47967329 | C | T | 120 | a0001c0001t0001g0067 a0002c0002t0002g0001 a0002c0002t0002g0004 others(117): Show |
121 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(118): Show |
intron_variant | MODIFIER | c.292+10536G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47967329 | |||||||
chr3:47967396 | C | T | 125 | a0001c0001t0001g0067 a0002c0002t0002g0001 a0002c0002t0002g0004 others(122): Show |
126 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.292+10469G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47967396 | |||||||
chr3:47967977 | C | T | 4 | a0001c0001t0001g0208 a0001c0001t0001g0210 a0001c0001t0001g0211 others(1): Show |
4 | HG01257.hp2 HG01258.hp1 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.292+9888G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47967977 | |||||||
chr3:47968146 | A | T | 1 | a0004c0004t0017g0086 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.292+9719T>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47968146 | |||||||
chr3:47968299 | G | A | 1 | a0002c0002t0004g0007 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.292+9566C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47968299 | |||||||
chr3:47968526 | T | C | 1 | a0014c0025t0001g0215 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.292+9339A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47968526 | |||||||
chr3:47968753 | A | C | 1 | a0023c0022t0002g0088 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.292+9112T>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47968753 | |||||||
chr3:47968818 | G | C | 16 | a0003c0003t0003g0095 a0003c0003t0003g0098 a0003c0003t0003g0099 others(13): Show |
16 | HG01109.hp2 HG02055.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.292+9047C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47968818 | |||||||
chr3:47969045 | AC | A | 3 | a0010c0013t0010g0002 a0010c0013t0010g0222 a0021c0028t0002g0224 |
3 | HG02145.hp2 HG02451.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.292+8819delG | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47969045 | |||||||
chr3:47969416 | G | A | 8 | a0002c0002t0002g0082 a0002c0002t0002g0130 a0006c0006t0002g0062 others(5): Show |
8 | HG01123.hp2 HG02145.hp1 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.292+8449C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47969416 | |||||||
chr3:47969468 | A | C | 1 | a0002c0002t0002g0035 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.292+8397T>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47969468 | |||||||
chr3:47969797 | T | C | 6 | a0004c0004t0002g0083 a0004c0004t0002g0084 a0004c0004t0002g0085 others(3): Show |
6 | HG02040.hp2 HG02071.hp2 HG02083.hp2 others(3): Show |
intron_variant | MODIFIER | c.292+8068A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47969797 | |||||||
chr3:47969846 | C | T | 1 | a0002c0002t0002g0082 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.292+8019G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47969846 | |||||||
chr3:47969847 | A | G | 224 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(221): Show |
225 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(222): Show |
intron_variant | MODIFIER | c.292+8018T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47969847 | |||||||
chr3:47970118 | A | C | 2 | a0004c0004t0011g0049 a0004c0004t0011g0050 |
2 | HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.292+7747T>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47970118 | |||||||
chr3:47970148 | A | G | 125 | a0001c0001t0001g0067 a0002c0002t0002g0001 a0002c0002t0002g0004 others(122): Show |
126 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.292+7717T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47970148 | |||||||
chr3:47970154 | T | C | 1 | a0022c0030t0023g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.292+7711A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47970154 | |||||||
chr3:47970615 | G | A | 4 | a0002c0002t0002g0089 a0002c0002t0002g0091 a0002c0002t0002g0092 others(1): Show |
4 | NA18941.hp1 NA18943.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.292+7250C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47970615 | |||||||
chr3:47970892 | T | C | 1 | a0001c0001t0012g0204 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.292+6973A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47970892 | |||||||
chr3:47970937 | T | C | 2 | a0002c0002t0002g0037 a0002c0002t0002g0039 |
2 | HG02135.hp1 NA18946.hp1 |
intron_variant | MODIFIER | c.292+6928A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47970937 | |||||||
chr3:47971043 | G | C | 1 | a0021c0028t0002g0224 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.292+6822C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47971043 | |||||||
chr3:47971092 | C | T | 1 | a0002c0002t0002g0118 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.292+6773G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47971092 | |||||||
chr3:47971199 | G | C | 3 | a0009c0009t0002g0046 a0009c0009t0002g0047 a0009c0009t0002g0048 |
3 | HG01891.hp2 HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.292+6666C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47971199 | |||||||
chr3:47971307 | C | T | 121 | a0001c0001t0001g0067 a0002c0002t0002g0001 a0002c0002t0002g0004 others(118): Show |
122 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.292+6558G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47971307 | |||||||
chr3:47971485 | T | C | 1 | a0002c0002t0002g0082 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.292+6380A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47971485 | |||||||
chr3:47971722 | G | A | 16 | a0003c0003t0003g0095 a0003c0003t0003g0098 a0003c0003t0003g0099 others(13): Show |
16 | HG01109.hp2 HG02055.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.292+6143C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47971722 | |||||||
chr3:47971894 | G | A | 1 | a0001c0001t0009g0205 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.292+5971C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47971894 | |||||||
chr3:47971959 | G | C | 1 | a0001c0001t0001g0146 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.292+5906C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47971959 | |||||||
chr3:47971986 | A | G | 1 | a0022c0030t0023g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.292+5879T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47971986 | |||||||
chr3:47972172 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.292+5693C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47972172 | |||||||
chr3:47972402 | G | C | 1 | a0002c0020t0002g0054 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.292+5463C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47972402 | |||||||
chr3:47972519 | T | C | 1 | a0002c0002t0002g0123 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.292+5346A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47972519 | |||||||
chr3:47972715 | C | T | 125 | a0001c0001t0001g0067 a0002c0002t0002g0001 a0002c0002t0002g0004 others(122): Show |
126 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.292+5150G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47972715 | |||||||
chr3:47973093 | A | C | 2 | a0004c0004t0011g0049 a0004c0004t0011g0050 |
2 | HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.292+4772T>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47973093 | |||||||
chr3:47973263 | G | GA | 27 | a0001c0001t0001g0179 a0003c0003t0003g0095 a0003c0003t0003g0098 others(24): Show |
27 | HG00738.hp1 HG01109.hp2 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.292+4601dupT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47973263 | |||||||
chr3:47973473 | G | A | 1 | a0020c0023t0002g0053 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.292+4392C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47973473 | |||||||
chr3:47973701 | A | G | 1 | a0001c0001t0001g0230 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.292+4164T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47973701 | |||||||
chr3:47973788 | G | A | 1 | a0010c0013t0010g0002 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.292+4077C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47973788 | |||||||
chr3:47974102 | A | C | 1 | a0002c0002t0002g0012 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.292+3763T>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47974102 | |||||||
chr3:47974471 | C | G | 1 | a0001c0007t0001g0220 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.292+3394G>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47974471 | |||||||
chr3:47974596 | A | G | 9 | a0002c0002t0002g0052 a0002c0002t0002g0089 a0002c0002t0002g0090 others(6): Show |
9 | HG02015.hp2 NA18747.hp1 NA18941.hp1 others(6): Show |
intron_variant | MODIFIER | c.292+3269T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47974596 | |||||||
chr3:47974682 | T | C | 120 | a0001c0001t0001g0067 a0002c0002t0002g0001 a0002c0002t0002g0004 others(117): Show |
121 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(118): Show |
intron_variant | MODIFIER | c.292+3183A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47974682 | |||||||
chr3:47974727 | C | T | 9 | a0002c0002t0002g0052 a0002c0002t0002g0089 a0002c0002t0002g0090 others(6): Show |
9 | HG02015.hp2 NA18747.hp1 NA18941.hp1 others(6): Show |
intron_variant | MODIFIER | c.292+3138G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47974727 | |||||||
chr3:47974910 | G | C | 1 | a0002c0002t0002g0072 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.292+2955C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47974910 | |||||||
chr3:47975377 | G | A | 1 | a0001c0001t0009g0178 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.292+2488C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47975377 | |||||||
chr3:47975858 | C | T | 2 | a0011c0015t0003g0096 a0011c0015t0003g0097 |
2 | HG02717.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.292+2007G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47975858 | |||||||
chr3:47975892 | C | T | 1 | a0002c0002t0002g0082 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.292+1973G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47975892 | |||||||
chr3:47975936 | C | T | 1 | a0002c0002t0002g0033 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.292+1929G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47975936 | |||||||
chr3:47976127 | A | G | 125 | a0001c0001t0001g0067 a0002c0002t0002g0001 a0002c0002t0002g0004 others(122): Show |
126 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.292+1738T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47976127 | |||||||
chr3:47976221 | C | T | 7 | a0002c0002t0002g0027 a0002c0002t0002g0029 a0002c0002t0002g0030 others(4): Show |
7 | HG00544.hp2 HG02735.hp1 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.292+1644G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47976221 | |||||||
chr3:47976343 | A | G | 1 | a0019c0018t0002g0023 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.292+1522T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47976343 | |||||||
chr3:47976916 | C | T | 1 | a0002c0002t0005g0028 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.292+949G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47976916 | |||||||
chr3:47976942 | A | G | 1 | a0001c0001t0001g0139 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.292+923T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47976942 | |||||||
chr3:47977223 | T | C | 1 | a0021c0028t0002g0224 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.292+642A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47977223 | |||||||
chr3:47977278 | C | T | 1 | a0002c0002t0002g0130 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.292+587G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47977278 | |||||||
chr3:47977381 | T | C | 2 | a0001c0001t0008g0166 a0001c0001t0008g0167 |
2 | HG02258.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.292+484A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47977381 | |||||||
chr3:47977691 | T | C | 1 | a0021c0028t0002g0224 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.292+174A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47977691 | |||||||
chr3:47977742 | A | G | 104 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(101): Show |
104 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.292+123T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47977742 | |||||||
chr3:47977768 | A | G | 104 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(101): Show |
104 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.292+97T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | 47977768 | |||||||
chr3:47978030 | T | C | 1 | a0023c0022t0002g0088 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.224-97A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47978030 | |||||||
chr3:47978264 | T | A | 1 | a0001c0001t0001g0194 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.224-331A>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47978264 | |||||||
chr3:47978531 | G | A | 1 | a0023c0022t0002g0088 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.224-598C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47978531 | |||||||
chr3:47978647 | A | T | 1 | a0001c0001t0001g0128 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.224-714T>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47978647 | |||||||
chr3:47978673 | T | C | 2 | a0001c0001t0022g0213 a0014c0025t0001g0215 |
2 | HG00544.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.224-740A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47978673 | |||||||
chr3:47978771 | T | C | 1 | a0021c0028t0002g0224 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.224-838A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47978771 | |||||||
chr3:47979178 | G | T | 1 | a0025c0031t0003g0109 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.224-1245C>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47979178 | |||||||
chr3:47979184 | G | A | 2 | a0001c0001t0001g0147 a0001c0001t0001g0156 |
2 | HG03831.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.224-1251C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47979184 | |||||||
chr3:47979206 | AAGTTTCT others(31): Show |
A | 1 | a0002c0002t0002g0123 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.224-1311_224-1274d others(40): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47979206 | |||||||
chr3:47979528 | G | A | 104 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(101): Show |
104 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.224-1595C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47979528 | |||||||
chr3:47979599 | G | C | 3 | a0009c0009t0002g0046 a0009c0009t0002g0047 a0009c0009t0002g0048 |
3 | HG01891.hp2 HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.224-1666C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47979599 | |||||||
chr3:47979604 | G | A | 2 | a0004c0004t0011g0049 a0004c0004t0011g0050 |
2 | HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.224-1671C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47979604 | |||||||
chr3:47979613 | C | A | 2 | a0010c0013t0010g0222 a0021c0028t0002g0224 |
2 | HG02145.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.224-1680G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47979613 | |||||||
chr3:47979624 | T | A | 1 | a0001c0001t0009g0205 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.224-1691A>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47979624 | |||||||
chr3:47979792 | C | T | 40 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(37): Show |
40 | HG00544.hp1 HG00609.hp2 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.224-1859G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47979792 | |||||||
chr3:47979901 | T | C | 1 | a0001c0007t0001g0220 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.224-1968A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47979901 | |||||||
chr3:47981083 | A | C | 109 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(106): Show |
109 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.224-3150T>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47981083 | |||||||
chr3:47981217 | T | C | 104 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(101): Show |
104 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.224-3284A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47981217 | |||||||
chr3:47981478 | A | T | 1 | a0001c0001t0001g0139 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.224-3545T>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47981478 | |||||||
chr3:47981719 | C | T | 3 | a0001c0001t0001g0164 a0001c0001t0001g0181 a0001c0001t0001g0182 |
3 | HG01123.hp1 HG01943.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.224-3786G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47981719 | |||||||
chr3:47981766 | C | CA | 6 | a0001c0001t0001g0157 a0002c0002t0002g0035 a0002c0002t0002g0039 others(3): Show |
6 | HG02135.hp1 HG02145.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.224-3834dupT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47981766 | |||||||
chr3:47982083 | G | A | 1 | a0004c0004t0002g0085 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.224-4150C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47982083 | |||||||
chr3:47982271 | C | A | 29 | a0003c0003t0003g0095 a0003c0003t0003g0098 a0003c0003t0003g0099 others(26): Show |
29 | HG00738.hp1 HG01109.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.224-4338G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47982271 | |||||||
chr3:47982434 | G | C | 57 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(54): Show |
57 | HG00099.hp1 HG00280.hp1 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.224-4501C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47982434 | |||||||
chr3:47982841 | T | G | 29 | a0003c0003t0003g0095 a0003c0003t0003g0098 a0003c0003t0003g0099 others(26): Show |
29 | HG00738.hp1 HG01109.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.224-4908A>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47982841 | |||||||
chr3:47982870 | A | C | 1 | a0013c0014t0001g0142 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.224-4937T>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47982870 | |||||||
chr3:47982934 | A | G | 6 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0177 others(3): Show |
6 | NA18943.hp1 NA18946.hp2 NA18956.hp2 others(3): Show |
intron_variant | MODIFIER | c.224-5001T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47982934 | |||||||
chr3:47983053 | C | G | 3 | a0009c0009t0002g0046 a0009c0009t0002g0047 a0009c0009t0002g0048 |
3 | HG01891.hp2 HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.224-5120G>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47983053 | |||||||
chr3:47983139 | A | T | 105 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(102): Show |
105 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.224-5206T>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47983139 | |||||||
chr3:47983482 | G | A | 1 | a0023c0022t0002g0088 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.224-5549C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47983482 | |||||||
chr3:47983490 | G | A | 1 | a0004c0004t0020g0080 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.224-5557C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47983490 | |||||||
chr3:47983533 | T | C | 227 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(224): Show |
228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.224-5600A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47983533 | |||||||
chr3:47983547 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.224-5614G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47983547 | |||||||
chr3:47983639 | C | T | 3 | a0010c0013t0010g0002 a0010c0013t0010g0222 a0021c0028t0002g0224 |
3 | HG02145.hp2 HG02451.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.224-5706G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47983639 | |||||||
chr3:47983654 | C | T | 1 | a0015c0021t0002g0011 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.224-5721G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47983654 | |||||||
chr3:47983661 | T | G | 1 | a0002c0002t0005g0040 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.224-5728A>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47983661 | |||||||
chr3:47983822 | T | C | 1 | a0001c0001t0001g0195 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.224-5889A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47983822 | |||||||
chr3:47984632 | G | C | 3 | a0010c0013t0010g0002 a0010c0013t0010g0222 a0021c0028t0002g0224 |
3 | HG02145.hp2 HG02451.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.224-6699C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47984632 | |||||||
chr3:47984669 | T | TA | 10 | a0004c0004t0002g0083 a0004c0004t0002g0084 a0004c0004t0002g0085 others(7): Show |
10 | HG01934.hp1 HG02040.hp2 HG02071.hp2 others(7): Show |
intron_variant | MODIFIER | c.224-6737dupT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47984669 | |||||||
chr3:47984682 | A | G | 1 | a0001c0001t0001g0229 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.224-6749T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47984682 | |||||||
chr3:47984684 | A | G | 1 | a0001c0001t0001g0229 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.224-6751T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47984684 | |||||||
chr3:47984796 | C | A | 1 | a0004c0004t0017g0086 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.224-6863G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47984796 | |||||||
chr3:47985117 | C | T | 221 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(218): Show |
222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.224-7184G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47985117 | |||||||
chr3:47985125 | C | G | 2 | a0004c0004t0018g0060 a0004c0004t0020g0080 |
2 | HG01934.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.224-7192G>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47985125 | |||||||
chr3:47985383 | G | T | 1 | a0001c0001t0001g0210 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.224-7450C>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47985383 | |||||||
chr3:47985475 | T | A | 1 | a0002c0002t0002g0058 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.224-7542A>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47985475 | |||||||
chr3:47985915 | T | C | 1 | a0004c0004t0002g0223 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.224-7982A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47985915 | |||||||
chr3:47986159 | G | A | 1 | a0023c0022t0002g0088 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.224-8226C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47986159 | |||||||
chr3:47986342 | G | T | 148 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(145): Show |
148 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(145): Show |
intron_variant | MODIFIER | c.224-8409C>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47986342 | |||||||
chr3:47986353 | T | A | 1 | a0001c0001t0001g0172 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.224-8420A>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47986353 | |||||||
chr3:47986361 | G | T | 104 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(101): Show |
104 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.224-8428C>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47986361 | |||||||
chr3:47986474 | G | A | 2 | a0001c0001t0001g0196 a0001c0001t0001g0197 |
2 | HG01109.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.224-8541C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47986474 | |||||||
chr3:47986481 | C | T | 3 | a0009c0009t0002g0046 a0009c0009t0002g0047 a0009c0009t0002g0048 |
3 | HG01891.hp2 HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.224-8548G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47986481 | |||||||
chr3:47986486 | G | A | 1 | a0022c0030t0023g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.224-8553C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47986486 | |||||||
chr3:47986654 | T | A | 104 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(101): Show |
104 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.224-8721A>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47986654 | |||||||
chr3:47986696 | G | A | 1 | a0001c0007t0001g0221 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.224-8763C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47986696 | |||||||
chr3:47986698 | TA | T | 3 | a0001c0001t0001g0164 a0001c0001t0001g0181 a0001c0001t0001g0182 |
3 | HG01123.hp1 HG01943.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.224-8766delT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47986698 | |||||||
chr3:47986878 | C | T | 3 | a0002c0002t0002g0021 a0002c0002t0002g0024 a0019c0018t0002g0023 |
3 | HG01496.hp2 HG01943.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.224-8945G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47986878 | |||||||
chr3:47987146 | T | C | 7 | a0002c0002t0002g0027 a0002c0002t0002g0029 a0002c0002t0002g0030 others(4): Show |
7 | HG00544.hp2 HG02735.hp1 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.224-9213A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47987146 | |||||||
chr3:47987214 | T | C | 1 | a0002c0002t0002g0039 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.224-9281A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47987214 | |||||||
chr3:47987287 | G | C | 2 | a0001c0001t0001g0206 a0001c0001t0001g0217 |
2 | NA18983.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.224-9354C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47987287 | |||||||
chr3:47987307 | G | A | 1 | a0010c0013t0010g0002 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.224-9374C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47987307 | |||||||
chr3:47987337 | A | G | 1 | a0010c0013t0010g0002 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.224-9404T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47987337 | |||||||
chr3:47987421 | G | A | 1 | a0004c0004t0002g0084 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.224-9488C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47987421 | |||||||
chr3:47987628 | A | C | 109 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(106): Show |
109 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.224-9695T>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47987628 | |||||||
chr3:47987916 | C | G | 1 | a0012c0012t0002g0078 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.224-9983G>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47987916 | |||||||
chr3:47988257 | ATT | A | 104 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(101): Show |
104 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.224-10326_224-1032 others(6): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47988257 | |||||||
chr3:47988282 | T | A | 1 | a0004c0004t0002g0084 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.224-10349A>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47988282 | |||||||
chr3:47988456 | T | C | 1 | a0002c0002t0002g0082 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.223+10182A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47988456 | |||||||
chr3:47988512 | G | A | 2 | a0001c0001t0001g0206 a0001c0001t0001g0217 |
2 | NA18983.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.223+10126C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47988512 | |||||||
chr3:47988660 | A | G | 3 | a0010c0013t0010g0002 a0010c0013t0010g0222 a0021c0028t0002g0224 |
3 | HG02145.hp2 HG02451.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.223+9978T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47988660 | |||||||
chr3:47988861 | T | G | 148 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(145): Show |
148 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(145): Show |
intron_variant | MODIFIER | c.223+9777A>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47988861 | |||||||
chr3:47988970 | C | T | 1 | a0010c0013t0010g0002 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.223+9668G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47988970 | |||||||
chr3:47989046 | G | A | 2 | a0010c0013t0010g0222 a0021c0028t0002g0224 |
2 | HG02145.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.223+9592C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47989046 | |||||||
chr3:47989409 | A | T | 1 | a0002c0002t0002g0018 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.223+9229T>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47989409 | |||||||
chr3:47989590 | T | C | 1 | a0004c0004t0018g0060 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.223+9048A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47989590 | |||||||
chr3:47989676 | C | T | 2 | a0008c0010t0007g0111 a0008c0010t0007g0112 |
2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.223+8962G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47989676 | |||||||
chr3:47989677 | G | GT | 2 | a0001c0001t0001g0127 a0001c0001t0001g0136 |
2 | HG03139.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.223+8960dupA | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47989677 | |||||||
chr3:47989806 | A | G | 3 | a0010c0013t0010g0002 a0010c0013t0010g0222 a0021c0028t0002g0224 |
3 | HG02145.hp2 HG02451.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.223+8832T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47989806 | |||||||
chr3:47990202 | A | T | 4 | a0001c0001t0001g0134 a0001c0001t0001g0144 a0001c0001t0001g0145 others(1): Show |
4 | HG00639.hp2 HG00733.hp2 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.223+8436T>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47990202 | |||||||
chr3:47990309 | A | G | 1 | a0001c0001t0001g0158 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.223+8329T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47990309 | |||||||
chr3:47990561 | G | A | 1 | a0022c0030t0023g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.223+8077C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47990561 | |||||||
chr3:47990677 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.223+7961T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47990677 | |||||||
chr3:47990723 | G | A | 2 | a0002c0002t0004g0015 a0002c0002t0004g0016 |
2 | NA19005.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.223+7915C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47990723 | |||||||
chr3:47990842 | A | AT | 225 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(222): Show |
226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.223+7795dupA | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47990842 | |||||||
chr3:47990867 | G | T | 104 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(101): Show |
104 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.223+7771C>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47990867 | |||||||
chr3:47991451 | G | A | 4 | a0002c0002t0002g0091 a0010c0013t0010g0002 a0010c0013t0010g0222 others(1): Show |
4 | HG02145.hp2 HG02451.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.223+7187C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47991451 | |||||||
chr3:47991459 | C | T | 1 | a0002c0002t0002g0063 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.223+7179G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47991459 | |||||||
chr3:47991686 | C | T | 2 | a0004c0004t0018g0060 a0004c0004t0020g0080 |
2 | HG01934.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.223+6952G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47991686 | |||||||
chr3:47991713 | G | A | 1 | a0004c0004t0018g0060 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.223+6925C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47991713 | |||||||
chr3:47992036 | G | A | 1 | a0023c0022t0002g0088 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.223+6602C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47992036 | |||||||
chr3:47992300 | G | A | 2 | a0004c0004t0018g0060 a0004c0004t0020g0080 |
2 | HG01934.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.223+6338C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47992300 | |||||||
chr3:47992563 | G | T | 1 | a0002c0002t0002g0012 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.223+6075C>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47992563 | |||||||
chr3:47992584 | C | T | 2 | a0011c0015t0003g0096 a0011c0015t0003g0097 |
2 | HG02717.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.223+6054G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47992584 | |||||||
chr3:47992685 | T | C | 31 | a0002c0002t0002g0004 a0002c0002t0002g0005 a0002c0002t0002g0010 others(28): Show |
31 | HG00099.hp2 HG00597.hp2 HG00673.hp2 others(28): Show |
intron_variant | MODIFIER | c.223+5953A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47992685 | |||||||
chr3:47992903 | T | TA | 22 | a0001c0001t0001g0229 a0002c0002t0004g0017 a0002c0002t0019g0064 others(19): Show |
22 | HG01109.hp2 HG02040.hp1 HG02040.hp2 others(19): Show |
intron_variant | MODIFIER | c.223+5734dupT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47992903 | |||||||
chr3:47992903 | TA | T | 6 | a0001c0024t0001g0133 a0002c0002t0002g0004 a0002c0002t0002g0005 others(3): Show |
6 | HG00280.hp1 HG01074.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.223+5734delT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47992903 | |||||||
chr3:47993195 | G | A | 1 | a0003c0003t0021g0105 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.223+5443C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47993195 | |||||||
chr3:47993927 | C | T | 1 | a0001c0001t0001g0128 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.223+4711G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47993927 | |||||||
chr3:47993961 | A | G | 1 | a0004c0004t0002g0223 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.223+4677T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47993961 | |||||||
chr3:47994068 | T | C | 1 | a0001c0001t0001g0229 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.223+4570A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47994068 | |||||||
chr3:47994948 | C | CA | 23 | a0001c0001t0001g0129 a0001c0001t0001g0158 a0001c0001t0001g0162 others(20): Show |
23 | HG01109.hp2 HG01516.hp2 HG02135.hp2 others(20): Show |
intron_variant | MODIFIER | c.223+3689dupT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47994948 | |||||||
chr3:47995250 | C | CT | 13 | a0002c0002t0002g0030 a0002c0002t0002g0036 a0002c0002t0002g0039 others(10): Show |
13 | HG01891.hp2 HG02135.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.223+3387dupA | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47995250 | |||||||
chr3:47995250 | CT | C | 103 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(100): Show |
103 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.223+3387delA | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47995250 | |||||||
chr3:47995399 | C | T | 3 | a0010c0013t0010g0002 a0010c0013t0010g0222 a0021c0028t0002g0224 |
3 | HG02145.hp2 HG02451.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.223+3239G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47995399 | |||||||
chr3:47995531 | G | A | 1 | a0023c0022t0002g0088 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.223+3107C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47995531 | |||||||
chr3:47995588 | G | A | 109 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(106): Show |
109 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.223+3050C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47995588 | |||||||
chr3:47995621 | C | G | 2 | a0013c0014t0001g0142 a0013c0014t0001g0143 |
2 | NA19007.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.223+3017G>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47995621 | |||||||
chr3:47995697 | C | T | 1 | a0022c0030t0023g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.223+2941G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47995697 | |||||||
chr3:47995722 | A | G | 1 | a0008c0010t0007g0112 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.223+2916T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47995722 | |||||||
chr3:47995851 | T | C | 1 | a0002c0002t0002g0057 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.223+2787A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47995851 | |||||||
chr3:47996042 | T | C | 1 | a0002c0002t0002g0066 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.223+2596A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47996042 | |||||||
chr3:47996124 | T | C | 2 | a0001c0001t0001g0198 a0001c0001t0001g0199 |
2 | NA18963.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.223+2514A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47996124 | |||||||
chr3:47996599 | G | C | 1 | a0001c0007t0001g0221 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.223+2039C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47996599 | |||||||
chr3:47996737 | G | GAC | 5 | a0001c0001t0001g0227 a0002c0002t0002g0055 a0002c0011t0002g0073 others(2): Show |
5 | HG00733.hp1 HG02559.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.223+1899_223+1900d others(4): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47996737 | |||||||
chr3:47996737 | G | GACAC | 39 | a0002c0002t0002g0004 a0002c0002t0002g0005 a0002c0002t0002g0010 others(36): Show |
39 | HG00099.hp2 HG00544.hp2 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.223+1897_223+1900d others(6): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47996737 | |||||||
chr3:47996737 | G | GACACAC | 9 | a0004c0004t0002g0083 a0004c0004t0002g0084 a0004c0004t0002g0085 others(6): Show |
9 | HG00597.hp2 HG01934.hp1 HG02040.hp2 others(6): Show |
intron_variant | MODIFIER | c.223+1895_223+1900d others(8): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47996737 | |||||||
chr3:47996737 | G | GACACACA others(1): Show |
18 | a0003c0003t0003g0095 a0003c0003t0003g0098 a0003c0003t0003g0099 others(15): Show |
18 | HG01109.hp2 HG01891.hp2 HG02630.hp1 others(15): Show |
intron_variant | MODIFIER | c.223+1893_223+1900d others(10): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47996737 | |||||||
chr3:47996737 | G | GACACACA others(3): Show |
9 | a0004c0004t0011g0049 a0004c0004t0018g0060 a0005c0005t0003g0114 others(6): Show |
9 | HG02258.hp1 HG02486.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.223+1891_223+1900d others(12): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47996737 | |||||||
chr3:47996737 | G | GACACACA others(5): Show |
2 | a0003c0003t0003g0107 a0005c0005t0003g0121 |
2 | HG02055.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.223+1889_223+1900d others(14): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47996737 | |||||||
chr3:47996737 | G | GACACACA others(9): Show |
2 | a0005c0005t0003g0115 a0005c0005t0003g0117 |
2 | HG01884.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.223+1885_223+1900d others(18): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47996737 | |||||||
chr3:47996737 | G | GACACACA others(11): Show |
1 | a0008c0010t0007g0112 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.223+1883_223+1900d others(20): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47996737 | |||||||
chr3:47996737 | G | GACACACA others(13): Show |
1 | a0008c0010t0007g0113 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.223+1881_223+1900d others(22): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47996737 | |||||||
chr3:47996737 | GAC | G | 10 | a0001c0001t0001g0126 a0001c0001t0001g0161 a0001c0001t0001g0162 others(7): Show |
10 | HG00609.hp1 HG00609.hp2 HG00673.hp1 others(7): Show |
intron_variant | MODIFIER | c.223+1899_223+1900d others(4): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47996737 | |||||||
chr3:47996737 | GACAC | G | 94 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(91): Show |
94 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.223+1897_223+1900d others(6): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47996737 | |||||||
chr3:47997224 | C | T | 104 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(101): Show |
104 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.223+1414G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47997224 | |||||||
chr3:47997276 | CAAG | C | 2 | a0002c0002t0002g0037 a0002c0002t0002g0039 |
2 | HG02135.hp1 NA18946.hp1 |
intron_variant | MODIFIER | c.223+1359_223+1361d others(5): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47997276 | |||||||
chr3:47997326 | T | TAAAAAA | 5 | a0002c0002t0002g0063 a0002c0002t0005g0040 a0002c0002t0019g0064 others(2): Show |
5 | HG00280.hp2 HG01074.hp2 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.223+1306_223+1311d others(8): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47997326 | |||||||
chr3:47997326 | T | TAAAAAAA others(2): Show |
10 | a0005c0005t0003g0114 a0005c0005t0003g0115 a0005c0005t0003g0116 others(7): Show |
10 | HG00738.hp1 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.223+1303_223+1311d others(11): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47997326 | |||||||
chr3:47997326 | T | TAAAAAAA others(3): Show |
13 | a0003c0003t0003g0095 a0003c0003t0003g0100 a0003c0003t0003g0101 others(10): Show |
13 | HG01109.hp2 HG02717.hp2 HG02886.hp2 others(10): Show |
intron_variant | MODIFIER | c.223+1302_223+1311d others(12): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47997326 | |||||||
chr3:47997326 | T | TAAAAAAA others(4): Show |
8 | a0002c0002t0002g0082 a0002c0002t0002g0091 a0003c0003t0003g0107 others(5): Show |
8 | HG01891.hp2 HG01934.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.223+1301_223+1311d others(13): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47997326 | |||||||
chr3:47997326 | T | TAAAAAAA others(5): Show |
2 | a0004c0004t0011g0049 a0022c0030t0023g0044 |
2 | HG02486.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.223+1300_223+1311d others(14): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47997326 | |||||||
chr3:47997326 | T | TAAAAAAA others(6): Show |
6 | a0002c0002t0013g0065 a0004c0004t0002g0083 a0004c0004t0002g0084 others(3): Show |
6 | HG02071.hp2 HG02083.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.223+1299_223+1311d others(15): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47997326 | |||||||
chr3:47997326 | T | TAAAAAAA others(7): Show |
1 | a0004c0004t0002g0223 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.223+1298_223+1311d others(16): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47997326 | |||||||
chr3:47997326 | T | TAAAAAAA others(8): Show |
2 | a0002c0002t0002g0094 a0004c0004t0002g0085 |
2 | NA19000.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.223+1297_223+1311d others(17): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47997326 | |||||||
chr3:47997326 | T | TAAAAAAA others(9): Show |
1 | a0002c0002t0002g0057 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.223+1296_223+1311d others(18): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47997326 | |||||||
chr3:47997326 | T | TAAAAAAA others(10): Show |
2 | a0002c0002t0002g0092 a0002c0002t0002g0093 |
2 | NA18970.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.223+1295_223+1311d others(19): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47997326 | |||||||
chr3:47997326 | T | TAAAAAAA others(12): Show |
1 | a0002c0002t0002g0066 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.223+1293_223+1311d others(21): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47997326 | |||||||
chr3:47997326 | T | TAAAAAAA others(14): Show |
6 | a0002c0002t0002g0027 a0002c0002t0002g0029 a0002c0002t0002g0032 others(3): Show |
6 | HG00544.hp2 HG02145.hp1 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.223+1311_223+1312i others(23): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47997326 | |||||||
chr3:47997326 | T | TAAAAAAA others(15): Show |
14 | a0002c0002t0002g0004 a0002c0002t0002g0005 a0002c0002t0002g0025 others(11): Show |
14 | HG00099.hp2 HG02015.hp2 NA18747.hp1 others(11): Show |
intron_variant | MODIFIER | c.223+1311_223+1312i others(24): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47997326 | |||||||
chr3:47997326 | T | TAAAAAAA others(16): Show |
11 | a0002c0002t0002g0001 a0002c0002t0002g0010 a0002c0002t0002g0020 others(8): Show |
12 | HG00597.hp2 HG01257.hp1 HG01258.hp2 others(9): Show |
intron_variant | MODIFIER | c.223+1311_223+1312i others(25): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47997326 | |||||||
chr3:47997326 | T | TAAAAAAA others(17): Show |
7 | a0002c0002t0002g0012 a0002c0002t0002g0013 a0002c0002t0002g0014 others(4): Show |
7 | HG00673.hp2 HG00735.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.223+1311_223+1312i others(26): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47997326 | |||||||
chr3:47997326 | T | TAAAAAAA others(18): Show |
7 | a0002c0002t0002g0061 a0002c0002t0005g0026 a0002c0002t0005g0028 others(4): Show |
7 | HG01123.hp2 HG01169.hp2 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.223+1311_223+1312i others(27): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47997326 | |||||||
chr3:47997326 | T | TAAAAAAA others(19): Show |
1 | a0002c0011t0002g0087 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.223+1311_223+1312i others(28): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47997326 | |||||||
chr3:47997326 | T | TAAAAAAA others(20): Show |
3 | a0001c0001t0001g0067 a0002c0002t0002g0045 a0026c0019t0002g0077 |
3 | HG01516.hp1 HG03540.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.223+1311_223+1312i others(29): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47997326 | |||||||
chr3:47997326 | T | TAAAAAAA others(21): Show |
3 | a0002c0002t0002g0068 a0002c0002t0002g0069 a0028c0017t0002g0038 |
3 | HG01099.hp1 HG02615.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.223+1311_223+1312i others(30): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47997326 | |||||||
chr3:47997326 | T | TAAAAAAA others(22): Show |
1 | a0002c0002t0004g0016 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.223+1311_223+1312i others(31): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47997326 | |||||||
chr3:47997326 | T | TAAAAAAA others(23): Show |
3 | a0002c0002t0002g0051 a0006c0006t0002g0062 a0012c0012t0002g0071 |
3 | HG02300.hp1 HG02698.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.223+1311_223+1312i others(32): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47997326 | |||||||
chr3:47997326 | T | TAAAAAAA others(25): Show |
3 | a0002c0002t0002g0055 a0002c0002t0002g0072 a0002c0002t0002g0090 |
3 | HG03098.hp1 NA18998.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.223+1311_223+1312i others(34): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47997326 | |||||||
chr3:47997326 | T | TAAAAAAA others(26): Show |
1 | a0002c0002t0002g0123 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.223+1311_223+1312i others(35): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47997326 | |||||||
chr3:47997326 | T | TAAAAAAA others(27): Show |
1 | a0002c0002t0002g0089 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.223+1311_223+1312i others(36): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47997326 | |||||||
chr3:47997326 | T | TAAAAAAA others(28): Show |
2 | a0002c0002t0002g0056 a0002c0011t0002g0073 |
2 | HG00733.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.223+1311_223+1312i others(37): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47997326 | |||||||
chr3:47997326 | T | TAAAAAAA others(29): Show |
1 | a0002c0002t0002g0231 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.223+1311_223+1312i others(38): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47997326 | |||||||
chr3:47997326 | T | TAAAAAAA others(31): Show |
1 | a0002c0002t0002g0058 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.223+1311_223+1312i others(40): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47997326 | |||||||
chr3:47997326 | T | TAAAAAAA others(32): Show |
1 | a0012c0012t0002g0078 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.223+1311_223+1312i others(41): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47997326 | |||||||
chr3:47997326 | T | TAAAAAAA others(34): Show |
3 | a0002c0002t0002g0125 a0002c0020t0002g0054 a0027c0032t0002g0059 |
3 | HG02723.hp2 HG02976.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.223+1311_223+1312i others(43): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47997326 | |||||||
chr3:47997397 | T | C | 3 | a0009c0009t0002g0046 a0009c0009t0002g0047 a0009c0009t0002g0048 |
3 | HG01891.hp2 HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.223+1241A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47997397 | |||||||
chr3:47997707 | C | CAAAG | 11 | a0002c0002t0002g0090 a0004c0004t0002g0083 a0004c0004t0002g0084 others(8): Show |
11 | HG02040.hp2 HG02071.hp2 HG02083.hp2 others(8): Show |
intron_variant | MODIFIER | c.223+927_223+930dup others(4): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47997707 | |||||||
chr3:47997707 | C | CAAAGAAA others(5): Show |
3 | a0004c0004t0011g0049 a0004c0004t0011g0050 a0004c0004t0017g0086 |
3 | HG03041.hp2 HG03453.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.223+919_223+930dup others(12): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47997707 | |||||||
chr3:47997809 | T | G | 1 | a0022c0030t0023g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.223+829A>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47997809 | |||||||
chr3:47998418 | A | G | 4 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(1): Show |
4 | HG01255.hp1 HG02015.hp1 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.223+220T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47998418 | |||||||
chr3:47998540 | A | G | 1 | a0004c0004t0018g0060 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.223+98T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 2/20 | chr3 | 47998540 | |||||||
chr3:47999238 | T | C | 1 | a0023c0022t0002g0088 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-19-359A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 47999238 | |||||||
chr3:47999772 | C | A | 1 | a0001c0001t0001g0159 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-19-893G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 47999772 | |||||||
chr3:47999845 | TA | T | 121 | a0001c0001t0001g0067 a0001c0001t0001g0229 a0002c0002t0002g0001 others(118): Show |
122 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.-19-967delT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 47999845 | |||||||
chr3:47999845 | TAA | T | 104 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(101): Show |
104 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.-19-968_-19-967del others(2): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 47999845 | |||||||
chr3:47999981 | G | A | 16 | a0003c0003t0003g0095 a0003c0003t0003g0098 a0003c0003t0003g0099 others(13): Show |
16 | HG01109.hp2 HG02055.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.-19-1102C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 47999981 | |||||||
chr3:48000025 | G | T | 1 | a0002c0002t0002g0039 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-19-1146C>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48000025 | |||||||
chr3:48000130 | G | A | 1 | a0001c0001t0001g0136 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-19-1251C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48000130 | |||||||
chr3:48000221 | C | CA | 45 | a0001c0001t0001g0132 a0001c0001t0001g0227 a0002c0002t0002g0018 others(42): Show |
45 | HG00544.hp2 HG00738.hp1 HG01884.hp1 others(42): Show |
intron_variant | MODIFIER | c.-19-1343dupT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48000221 | |||||||
chr3:48000221 | C | CAA | 51 | a0001c0001t0001g0041 a0001c0001t0001g0043 a0001c0001t0001g0161 others(48): Show |
51 | HG00099.hp1 HG00280.hp1 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.-19-1344_-19-1343d others(4): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48000221 | |||||||
chr3:48000221 | C | CAAA | 11 | a0001c0001t0001g0042 a0001c0001t0001g0169 a0001c0001t0001g0170 others(8): Show |
11 | HG01074.hp1 HG02280.hp1 HG02602.hp2 others(8): Show |
intron_variant | MODIFIER | c.-19-1345_-19-1343d others(5): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48000221 | |||||||
chr3:48000221 | CAAAAAAA others(2): Show |
C | 44 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(41): Show |
44 | HG00544.hp1 HG00639.hp2 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.-19-1351_-19-1343d others(11): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48000221 | |||||||
chr3:48000257 | G | T | 1 | a0002c0002t0005g0026 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-19-1378C>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48000257 | |||||||
chr3:48000455 | G | T | 1 | a0001c0001t0001g0179 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-19-1576C>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48000455 | |||||||
chr3:48000702 | T | C | 13 | a0003c0003t0003g0095 a0003c0003t0003g0098 a0003c0003t0003g0099 others(10): Show |
13 | HG01109.hp2 HG02055.hp2 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.-19-1823A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48000702 | |||||||
chr3:48001018 | T | C | 1 | a0001c0001t0009g0178 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-19-2139A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48001018 | |||||||
chr3:48001232 | G | A | 1 | a0006c0006t0002g0079 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-19-2353C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48001232 | |||||||
chr3:48001350 | T | C | 1 | a0003c0003t0003g0108 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-19-2471A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48001350 | |||||||
chr3:48001568 | T | C | 148 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(145): Show |
148 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(145): Show |
intron_variant | MODIFIER | c.-19-2689A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48001568 | |||||||
chr3:48001917 | C | A | 1 | a0001c0001t0001g0160 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-19-3038G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48001917 | |||||||
chr3:48002206 | A | C | 1 | a0001c0001t0001g0162 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-19-3327T>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48002206 | |||||||
chr3:48002241 | C | CA | 3 | a0001c0001t0001g0206 a0001c0001t0001g0229 a0020c0023t0002g0053 |
3 | HG02071.hp2 HG02738.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.-19-3363dupT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48002241 | |||||||
chr3:48002246 | AG | A | 5 | a0001c0001t0001g0138 a0004c0004t0011g0049 a0004c0004t0011g0050 others(2): Show |
5 | HG01934.hp1 HG02015.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-19-3368delC | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48002246 | |||||||
chr3:48002247 | G | A | 143 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(140): Show |
143 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.-19-3368C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48002247 | |||||||
chr3:48002258 | G | GA | 11 | a0005c0005t0003g0114 a0005c0005t0003g0115 a0005c0005t0003g0116 others(8): Show |
11 | HG00738.hp1 HG01884.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.-19-3380dupT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48002258 | |||||||
chr3:48002606 | T | C | 1 | a0002c0011t0002g0087 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-19-3727A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48002606 | |||||||
chr3:48002755 | C | T | 1 | a0021c0028t0002g0224 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-19-3876G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48002755 | |||||||
chr3:48002769 | T | TACTC | 109 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(106): Show |
109 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.-19-3891_-19-3890i others(6): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48002769 | |||||||
chr3:48002912 | A | T | 2 | a0004c0004t0018g0060 a0004c0004t0020g0080 |
2 | HG01934.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.-19-4033T>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48002912 | |||||||
chr3:48002954 | A | AAAAT | 75 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(72): Show |
75 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(72): Show |
intron_variant | MODIFIER | c.-19-4079_-19-4076d others(6): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48002954 | |||||||
chr3:48002954 | A | AAAATAAA others(1): Show |
42 | a0001c0001t0001g0126 a0001c0001t0001g0128 a0001c0001t0001g0129 others(39): Show |
42 | HG00609.hp1 HG00609.hp2 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.-19-4083_-19-4076d others(10): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48002954 | |||||||
chr3:48002954 | A | AAAATAAA others(5): Show |
6 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0216 others(3): Show |
6 | HG02015.hp1 HG02486.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-4087_-19-4076d others(14): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48002954 | |||||||
chr3:48002954 | A | AAAATAAA others(9): Show |
1 | a0014c0025t0001g0215 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-19-4091_-19-4076d others(18): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48002954 | |||||||
chr3:48002954 | A | AAAATAAA others(13): Show |
2 | a0001c0001t0001g0214 a0001c0001t0022g0213 |
2 | NA19006.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.-19-4095_-19-4076d others(22): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48002954 | |||||||
chr3:48002954 | AAAAT | A | 13 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0005c0005t0003g0114 others(10): Show |
13 | HG00738.hp1 HG01884.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.-19-4079_-19-4076d others(6): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48002954 | |||||||
chr3:48002954 | AAAATAAA others(1): Show |
A | 3 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0002c0002t0002g0231 |
3 | HG00738.hp2 HG00741.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.-19-4083_-19-4076d others(10): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48002954 | |||||||
chr3:48002977 | A | ATAAAT | 3 | a0001c0001t0001g0127 a0001c0001t0001g0136 a0001c0001t0016g0135 |
3 | HG03139.hp1 NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-19-4103_-19-4099d others(7): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48002977 | |||||||
chr3:48002991 | A | AAATAAAT others(5): Show |
1 | a0010c0013t0010g0002 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-19-4113_-19-4112i others(14): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48002991 | |||||||
chr3:48002991 | A | AAATTAAT others(5): Show |
2 | a0010c0013t0010g0222 a0021c0028t0002g0224 |
2 | HG02145.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-19-4113_-19-4112i others(14): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48002991 | |||||||
chr3:48003453 | C | CA | 31 | a0002c0002t0002g0082 a0002c0002t0002g0123 a0002c0002t0002g0130 others(28): Show |
31 | HG00639.hp1 HG01123.hp2 HG01255.hp2 others(28): Show |
intron_variant | MODIFIER | c.-19-4575dupT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48003453 | |||||||
chr3:48003453 | CA | C | 5 | a0002c0020t0002g0054 a0009c0009t0002g0046 a0009c0009t0002g0047 others(2): Show |
5 | HG01891.hp2 HG02258.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.-19-4575delT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48003453 | |||||||
chr3:48003453 | CAA | C | 5 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0212 others(2): Show |
5 | HG01257.hp2 HG01934.hp2 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.-19-4576_-19-4575d others(4): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48003453 | |||||||
chr3:48003453 | CAAA | C | 94 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(91): Show |
94 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.-19-4577_-19-4575d others(5): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48003453 | |||||||
chr3:48003453 | CAAAA | C | 7 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(4): Show |
7 | HG01074.hp1 HG01169.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.-19-4578_-19-4575d others(6): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48003453 | |||||||
chr3:48003573 | CT | C | 27 | a0002c0002t0002g0004 a0002c0002t0002g0005 a0002c0002t0002g0010 others(24): Show |
27 | HG00099.hp2 HG00597.hp2 HG00673.hp2 others(24): Show |
intron_variant | MODIFIER | c.-19-4695delA | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48003573 | |||||||
chr3:48003647 | C | A | 105 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(102): Show |
105 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.-19-4768G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48003647 | |||||||
chr3:48003805 | A | G | 1 | a0023c0022t0002g0088 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-19-4926T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48003805 | |||||||
chr3:48003962 | C | T | 2 | a0001c0001t0001g0227 a0001c0001t0001g0228 |
2 | HG02559.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.-19-5083G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48003962 | |||||||
chr3:48004066 | T | C | 221 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(218): Show |
222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.-19-5187A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48004066 | |||||||
chr3:48004402 | A | G | 1 | a0001c0001t0001g0134 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-19-5523T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48004402 | |||||||
chr3:48004541 | G | A | 1 | a0004c0004t0002g0223 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-19-5662C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48004541 | |||||||
chr3:48004543 | T | C | 3 | a0010c0013t0010g0002 a0010c0013t0010g0222 a0021c0028t0002g0224 |
3 | HG02145.hp2 HG02451.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-19-5664A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48004543 | |||||||
chr3:48004576 | A | G | 1 | a0022c0030t0023g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-19-5697T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48004576 | |||||||
chr3:48004820 | C | T | 1 | a0002c0002t0002g0027 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-19-5941G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48004820 | |||||||
chr3:48004854 | A | G | 1 | a0022c0030t0023g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-19-5975T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48004854 | |||||||
chr3:48005114 | T | C | 221 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(218): Show |
222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.-19-6235A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48005114 | |||||||
chr3:48005186 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-19-6307G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48005186 | |||||||
chr3:48005218 | G | C | 16 | a0003c0003t0003g0095 a0003c0003t0003g0098 a0003c0003t0003g0099 others(13): Show |
16 | HG01109.hp2 HG02055.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.-19-6339C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48005218 | |||||||
chr3:48005254 | G | A | 1 | a0022c0030t0023g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-19-6375C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48005254 | |||||||
chr3:48005255 | G | A | 1 | a0022c0030t0023g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-19-6376C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48005255 | |||||||
chr3:48005256 | C | G | 1 | a0022c0030t0023g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-19-6377G>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48005256 | |||||||
chr3:48005258 | G | C | 1 | a0022c0030t0023g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-19-6379C>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48005258 | |||||||
chr3:48005261 | T | A | 1 | a0022c0030t0023g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-19-6382A>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48005261 | |||||||
chr3:48005305 | G | A | 2 | a0001c0001t0001g0227 a0001c0001t0001g0228 |
2 | HG02559.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.-19-6426C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48005305 | |||||||
chr3:48005335 | T | TG | 138 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(135): Show |
138 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(135): Show |
intron_variant | MODIFIER | c.-19-6457dupC | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48005335 | |||||||
chr3:48005410 | A | C | 104 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(101): Show |
104 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.-19-6531T>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48005410 | |||||||
chr3:48005553 | A | G | 29 | a0003c0003t0003g0095 a0003c0003t0003g0098 a0003c0003t0003g0099 others(26): Show |
29 | HG00738.hp1 HG01109.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.-19-6674T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48005553 | |||||||
chr3:48005698 | A | G | 2 | a0010c0013t0010g0222 a0021c0028t0002g0224 |
2 | HG02145.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-19-6819T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48005698 | |||||||
chr3:48006151 | T | C | 1 | a0002c0002t0002g0025 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-19-7272A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48006151 | |||||||
chr3:48006231 | C | CCA | 60 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(57): Show |
60 | HG00099.hp1 HG00280.hp1 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.-19-7353_-19-7352i others(4): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48006231 | |||||||
chr3:48006384 | C | T | 108 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(105): Show |
108 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.-19-7505G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48006384 | |||||||
chr3:48006498 | T | C | 1 | a0002c0002t0002g0020 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-19-7619A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48006498 | |||||||
chr3:48007037 | C | T | 3 | a0008c0010t0007g0111 a0008c0010t0007g0112 a0008c0010t0007g0113 |
3 | HG00738.hp1 HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-19-8158G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48007037 | |||||||
chr3:48007676 | C | CT | 30 | a0002c0002t0005g0026 a0003c0003t0003g0095 a0003c0003t0003g0098 others(27): Show |
30 | HG00738.hp1 HG01109.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.-20+8657dupA | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48007676 | |||||||
chr3:48007676 | CT | C | 107 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(104): Show |
107 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.-20+8657delA | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48007676 | |||||||
chr3:48007840 | T | A | 1 | a0002c0002t0002g0020 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-20+8494A>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48007840 | |||||||
chr3:48007940 | A | G | 1 | a0002c0002t0002g0045 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-20+8394T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48007940 | |||||||
chr3:48008006 | G | A | 9 | a0002c0002t0002g0052 a0002c0002t0002g0089 a0002c0002t0002g0090 others(6): Show |
9 | HG02015.hp2 NA18747.hp1 NA18941.hp1 others(6): Show |
intron_variant | MODIFIER | c.-20+8328C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48008006 | |||||||
chr3:48008612 | C | A | 4 | a0001c0001t0001g0214 a0001c0001t0001g0216 a0001c0001t0022g0213 others(1): Show |
4 | HG00544.hp1 NA18982.hp1 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.-20+7722G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48008612 | |||||||
chr3:48008701 | G | A | 1 | a0022c0030t0023g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-20+7633C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48008701 | |||||||
chr3:48008703 | G | A | 1 | a0003c0003t0003g0110 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-20+7631C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48008703 | |||||||
chr3:48008740 | C | T | 2 | a0001c0001t0001g0132 a0007c0008t0006g0131 |
2 | NA19240.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-20+7594G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48008740 | |||||||
chr3:48008767 | C | A | 1 | a0001c0001t0001g0217 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-20+7567G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48008767 | |||||||
chr3:48008950 | T | C | 1 | a0002c0002t0002g0094 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-20+7384A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48008950 | |||||||
chr3:48009066 | A | G | 16 | a0003c0003t0003g0095 a0003c0003t0003g0098 a0003c0003t0003g0099 others(13): Show |
16 | HG01109.hp2 HG02055.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.-20+7268T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48009066 | |||||||
chr3:48009440 | G | A | 3 | a0010c0013t0010g0002 a0010c0013t0010g0222 a0021c0028t0002g0224 |
3 | HG02145.hp2 HG02451.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-20+6894C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48009440 | |||||||
chr3:48009566 | A | C | 1 | a0002c0002t0002g0052 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-20+6768T>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48009566 | |||||||
chr3:48010238 | A | G | 1 | a0001c0001t0001g0225 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-20+6096T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48010238 | |||||||
chr3:48010321 | A | G | 1 | a0010c0013t0010g0002 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-20+6013T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48010321 | |||||||
chr3:48010495 | T | A | 26 | a0003c0003t0003g0095 a0003c0003t0003g0098 a0003c0003t0003g0099 others(23): Show |
26 | HG00738.hp1 HG01109.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.-20+5839A>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48010495 | |||||||
chr3:48010843 | C | T | 3 | a0010c0013t0010g0002 a0010c0013t0010g0222 a0021c0028t0002g0224 |
3 | HG02145.hp2 HG02451.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-20+5491G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48010843 | |||||||
chr3:48010902 | G | A | 2 | a0001c0007t0001g0218 a0001c0007t0001g0219 |
2 | HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-20+5432C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48010902 | |||||||
chr3:48011344 | C | T | 1 | a0002c0002t0002g0051 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-20+4990G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48011344 | |||||||
chr3:48011529 | C | T | 1 | a0002c0002t0004g0003 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-20+4805G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48011529 | |||||||
chr3:48011575 | A | G | 1 | a0005c0005t0003g0119 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-20+4759T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48011575 | |||||||
chr3:48011644 | T | C | 2 | a0001c0007t0001g0220 a0001c0007t0001g0221 |
2 | HG02451.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-20+4690A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48011644 | |||||||
chr3:48012057 | C | T | 2 | a0004c0004t0011g0049 a0004c0004t0011g0050 |
2 | HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-20+4277G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48012057 | |||||||
chr3:48012214 | A | G | 3 | a0009c0009t0002g0046 a0009c0009t0002g0047 a0009c0009t0002g0048 |
3 | HG01891.hp2 HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-20+4120T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48012214 | |||||||
chr3:48012429 | T | G | 23 | a0002c0002t0002g0004 a0002c0002t0002g0005 a0002c0002t0002g0010 others(20): Show |
23 | HG00099.hp2 HG00597.hp2 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.-20+3905A>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48012429 | |||||||
chr3:48012966 | CTGT | C | 104 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(101): Show |
104 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.-20+3365_-20+3367d others(5): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48012966 | |||||||
chr3:48012981 | T | C | 5 | a0002c0002t0002g0021 a0002c0002t0002g0022 a0002c0002t0002g0024 others(2): Show |
5 | HG00099.hp2 HG00673.hp2 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20+3353A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48012981 | |||||||
chr3:48013015 | G | A | 1 | a0002c0002t0002g0118 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-20+3319C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48013015 | |||||||
chr3:48013054 | A | G | 1 | a0002c0002t0002g0045 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-20+3280T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48013054 | |||||||
chr3:48013063 | A | G | 106 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(103): Show |
106 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.-20+3271T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48013063 | |||||||
chr3:48013709 | T | TA | 106 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(103): Show |
106 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.-20+2624dupT | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48013709 | |||||||
chr3:48013765 | C | G | 228 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(225): Show |
229 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.-20+2569G>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48013765 | |||||||
chr3:48013776 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-20+2558G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48013776 | |||||||
chr3:48013829 | A | G | 23 | a0002c0002t0002g0004 a0002c0002t0002g0005 a0002c0002t0002g0010 others(20): Show |
23 | HG00099.hp2 HG00597.hp2 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.-20+2505T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48013829 | |||||||
chr3:48014621 | T | C | 1 | a0002c0002t0002g0123 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-20+1713A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48014621 | |||||||
chr3:48014812 | A | G | 1 | a0001c0001t0001g0126 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-20+1522T>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48014812 | |||||||
chr3:48014911 | C | T | 228 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(225): Show |
229 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.-20+1423G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48014911 | |||||||
chr3:48014919 | T | C | 105 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(102): Show |
105 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.-20+1415A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48014919 | |||||||
chr3:48014966 | G | A | 3 | a0010c0013t0010g0002 a0010c0013t0010g0222 a0021c0028t0002g0224 |
3 | HG02145.hp2 HG02451.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-20+1368C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48014966 | |||||||
chr3:48015149 | C | A | 1 | a0004c0004t0002g0223 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-20+1185G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48015149 | |||||||
chr3:48015196 | T | A | 1 | a0021c0028t0002g0224 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-20+1138A>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48015196 | |||||||
chr3:48015321 | T | G | 4 | a0001c0001t0001g0225 a0001c0001t0001g0227 a0001c0001t0001g0228 others(1): Show |
4 | HG01884.hp2 HG02559.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.-20+1013A>C | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48015321 | |||||||
chr3:48015354 | G | A | 1 | a0001c0001t0001g0043 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-20+980C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48015354 | |||||||
chr3:48015413 | T | C | 1 | a0001c0001t0001g0229 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-20+921A>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48015413 | |||||||
chr3:48015657 | A | C | 41 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(38): Show |
41 | HG00099.hp2 HG00544.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.-20+677T>G | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48015657 | |||||||
chr3:48015957 | C | A | 1 | a0001c0001t0001g0230 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-20+377G>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48015957 | |||||||
chr3:48016113 | G | A | 1 | a0002c0002t0002g0231 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-20+221C>T | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48016113 | |||||||
chr3:48016220 | C | T | 1 | a0010c0013t0010g0002 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-20+114G>A | MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 1/20 | chr3 | 48016220 |