Item | Value |
---|---|
geneid | 3360 |
ensemblid | ENSG00000164270.19 |
hgncid | 5299 |
symbol | HTR4 |
name | 5-hydroxytryptamine receptor 4 |
refseq_nuc | NM_000870.7 |
refseq_prot | NP_000861.1 |
ensembl_nuc | ENST00000377888.8 |
ensembl_prot | ENSP00000367120.4 |
mane_status | MANE Select |
chr | chr5 |
start | 148481547 |
end | 148654527 |
strand | - |
ver | v1.2 |
region | chr5:148481547-148654527 |
region5000 | chr5:148476547-148659527 |
regionname0 | HTR4_chr5_148481547_148654527 |
regionname5000 | HTR4_chr5_148476547_148659527 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 388 | 304 | 84 | 37 | 141 | 10 | 30 | 105 | HTR4_chr5_148476547_148659527 | HTR4 | MDKLD others(383): Show |
chr5 | 148476547 | 148659527 |
a0002 | 0/0 | 388 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | MDKLD others(383): Show |
chr5 | 148476547 | 148659527 |
a0003 | 0/0 | 388 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | MDKLD others(383): Show |
chr5 | 148476547 | 148659527 |
a0004 | 0/0 | 388 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | MDKLD others(383): Show |
chr5 | 148476547 | 148659527 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1164 | 290 | 74 | 36 | 141 | 10 | 27 | HTR4_chr5_148476547_148659527 | HTR4 | ATGGA others(1159): Show |
chr5 | 148476547 | 148659527 | ||
a0001c0002 | 0/0 | 1164 | 8 | 8 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | ATGGA others(1159): Show |
chr5 | 148476547 | 148659527 | ||
a0001c0004 | 0/0 | 1164 | 2 | 0 | 1 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | ATGGA others(1159): Show |
chr5 | 148476547 | 148659527 | ||
a0001c0005 | 0/0 | 1164 | 2 | 1 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | ATGGA others(1159): Show |
chr5 | 148476547 | 148659527 | ||
a0001c0006 | 0/0 | 1164 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | ATGGA others(1159): Show |
chr5 | 148476547 | 148659527 | ||
a0001c0008 | 0/0 | 1164 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | ATGGA others(1159): Show |
chr5 | 148476547 | 148659527 | ||
a0002c0003 | 0/0 | 1164 | 4 | 4 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | ATGGA others(1159): Show |
chr5 | 148476547 | 148659527 | ||
a0003c0009 | 0/0 | 1164 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | ATGGA others(1159): Show |
chr5 | 148476547 | 148659527 | ||
a0004c0007 | 0/0 | 1164 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | ATGGA others(1159): Show |
chr5 | 148476547 | 148659527 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 3336 | 112 | 38 | 16 | 39 | 4 | 13 | HTR4_chr5_148476547_148659527 | HTR4 | AGATG others(3331): Show |
chr5 | 148476547 | 148659527 |
a0001c0001t0002 | 0/0 | 3336 | 66 | 3 | 6 | 48 | 4 | 5 | HTR4_chr5_148476547_148659527 | HTR4 | AGATG others(3331): Show |
chr5 | 148476547 | 148659527 |
a0001c0001t0003 | 0/0 | 3336 | 34 | 13 | 1 | 16 | 1 | 3 | HTR4_chr5_148476547_148659527 | HTR4 | AGATG others(3331): Show |
chr5 | 148476547 | 148659527 |
a0001c0001t0004 | 0/0 | 3336 | 20 | 0 | 0 | 20 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | AGATG others(3331): Show |
chr5 | 148476547 | 148659527 |
a0001c0001t0005 | 0/0 | 3336 | 14 | 0 | 7 | 4 | 0 | 3 | HTR4_chr5_148476547_148659527 | HTR4 | AGATG others(3331): Show |
chr5 | 148476547 | 148659527 |
a0001c0001t0006 | 0/0 | 3336 | 10 | 2 | 3 | 3 | 0 | 2 | HTR4_chr5_148476547_148659527 | HTR4 | AGATG others(3331): Show |
chr5 | 148476547 | 148659527 |
a0001c0001t0007 | 0/0 | 3336 | 9 | 0 | 0 | 8 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | AGATG others(3331): Show |
chr5 | 148476547 | 148659527 |
a0001c0001t0008 | 0/0 | 3336 | 2 | 2 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | AGATG others(3331): Show |
chr5 | 148476547 | 148659527 |
a0001c0001t0009 | 0/0 | 3336 | 4 | 4 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | AGATG others(3331): Show |
chr5 | 148476547 | 148659527 |
a0001c0001t0010 | 0/0 | 3336 | 3 | 3 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | AGATG others(3331): Show |
chr5 | 148476547 | 148659527 |
a0001c0001t0011 | 0/0 | 3336 | 3 | 2 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | AGATG others(3331): Show |
chr5 | 148476547 | 148659527 |
a0001c0001t0012 | 0/0 | 3336 | 2 | 2 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | AGATG others(3331): Show |
chr5 | 148476547 | 148659527 |
a0001c0001t0014 | 0/0 | 3336 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | AGATG others(3331): Show |
chr5 | 148476547 | 148659527 |
a0001c0001t0015 | 0/0 | 3336 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | AGATG others(3331): Show |
chr5 | 148476547 | 148659527 |
a0001c0001t0016 | 0/0 | 3336 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | AGATG others(3331): Show |
chr5 | 148476547 | 148659527 |
a0001c0001t0017 | 0/0 | 3336 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | AGATG others(3331): Show |
chr5 | 148476547 | 148659527 |
a0001c0001t0018 | 0/0 | 3336 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | AGATG others(3331): Show |
chr5 | 148476547 | 148659527 |
a0001c0001t0020 | 0/0 | 3336 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | AGATG others(3331): Show |
chr5 | 148476547 | 148659527 |
a0001c0001t0021 | 0/0 | 3336 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | AGATG others(3331): Show |
chr5 | 148476547 | 148659527 |
a0001c0001t0023 | 0/0 | 3336 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | AGATG others(3331): Show |
chr5 | 148476547 | 148659527 |
a0001c0001t0024 | 0/0 | 3336 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | AGATG others(3331): Show |
chr5 | 148476547 | 148659527 |
a0001c0001t0025 | 0/0 | 3336 | 1 | 0 | 0 | 0 | 1 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | AGATG others(3331): Show |
chr5 | 148476547 | 148659527 |
a0001c0001t0026 | 0/0 | 3336 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | AGATG others(3331): Show |
chr5 | 148476547 | 148659527 |
a0001c0002t0001 | 0/0 | 3336 | 3 | 3 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | AGATG others(3331): Show |
chr5 | 148476547 | 148659527 |
a0001c0002t0003 | 0/0 | 3336 | 3 | 3 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | AGATG others(3331): Show |
chr5 | 148476547 | 148659527 |
a0001c0002t0008 | 0/0 | 3336 | 2 | 2 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | AGATG others(3331): Show |
chr5 | 148476547 | 148659527 |
a0001c0004t0001 | 0/0 | 3336 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | AGATG others(3331): Show |
chr5 | 148476547 | 148659527 |
a0001c0004t0003 | 0/0 | 3336 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | AGATG others(3331): Show |
chr5 | 148476547 | 148659527 |
a0001c0005t0005 | 0/0 | 3336 | 2 | 1 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | AGATG others(3331): Show |
chr5 | 148476547 | 148659527 |
a0001c0006t0003 | 0/0 | 3336 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | AGATG others(3331): Show |
chr5 | 148476547 | 148659527 |
a0001c0008t0001 | 0/0 | 3336 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | AGATG others(3331): Show |
chr5 | 148476547 | 148659527 |
a0002c0003t0013 | 0/0 | 3336 | 2 | 2 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | AGATG others(3331): Show |
chr5 | 148476547 | 148659527 |
a0002c0003t0019 | 0/0 | 3336 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | AGATG others(3331): Show |
chr5 | 148476547 | 148659527 |
a0002c0003t0022 | 0/0 | 3336 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | AGATG others(3331): Show |
chr5 | 148476547 | 148659527 |
a0003c0009t0027 | 0/0 | 3336 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | AGATG others(3331): Show |
chr5 | 148476547 | 148659527 |
a0004c0007t0002 | 0/0 | 3336 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | AGATG others(3331): Show |
chr5 | 148476547 | 148659527 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0206 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0272 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0002g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0002g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0002g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0002g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0002g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0002g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0002g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0002g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0002g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0002g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0003g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0003g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0003g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0003g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0003g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0003g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0003g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0003g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0003g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0004g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0004g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0004g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0004g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0004g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0004g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0004g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0004g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0004g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0004g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0004g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0004g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0004g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0004g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0004g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0004g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0004g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0004g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0004g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0005g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0005g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0005g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0005g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0005g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0005g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0005g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0005g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0005g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0005g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0005g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0005g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0005g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0006g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0006g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0006g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0006g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0006g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0006g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0006g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0006g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0006g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0006g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0007g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0007g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0007g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0007g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0007g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0007g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0007g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0007g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0007g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0008g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0008g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0009g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0009g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0009g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0009g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0010g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0010g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0010g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0011g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0011g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0011g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0012g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0012g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0014g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0015g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0016g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0017g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0018g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0020g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0021g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0023g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0024g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0025g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0001t0026g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0002t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0002t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0002t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0002t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0002t0003g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0002t0003g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0002t0008g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0002t0008g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0004t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0004t0003g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0005t0005g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0005t0005g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0006t0003g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0001c0008t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0002c0003t0013g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0002c0003t0013g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0002c0003t0019g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0002c0003t0022g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0003c0009t0027g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
a0004c0007t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0025 | g0270 | EUR | GBR | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0016 | EUR | GBR | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0274 | EUR | GBR | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG00140 | hp2 | a0001 | c0001 | t0003 | g0127 | EUR | GBR | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0017 | EUR | FIN | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0263 | EUR | FIN | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | CHS | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | CHS | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | CHS | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | CHS | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG00438 | hp1 | a0001 | c0001 | t0014 | g0004 | EAS | CHS | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | CHS | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG00544 | hp1 | a0001 | c0001 | t0004 | g0297 | EAS | CHS | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG00544 | hp2 | a0001 | c0001 | t0007 | g0006 | EAS | CHS | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | CHS | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG00558 | hp2 | a0001 | c0001 | t0003 | g0111 | EAS | CHS | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | CHS | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | CHS | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | CHS | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | CHS | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | CHS | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | CHS | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG00673 | hp1 | a0001 | c0001 | t0003 | g0087 | EAS | CHS | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | CHS | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0292 | AMR | PUR | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0301 | AMR | PUR | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0299 | AMR | PUR | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0247 | AMR | PUR | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG01071 | hp1 | a0001 | c0001 | t0005 | g0001 | AMR | PUR | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0246 | AMR | PUR | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG01074 | hp2 | a0001 | c0001 | t0005 | g0001 | AMR | PUR | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0287 | AMR | PUR | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0290 | AMR | PUR | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0291 | AMR | PUR | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | PUR | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG01192 | hp2 | a0001 | c0001 | t0003 | g0119 | AMR | PUR | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG01243 | hp1 | a0003 | c0009 | t0027 | g0307 | AMR | PUR | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG01257 | hp1 | a0001 | c0001 | t0006 | g0241 | AMR | CLM | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG01257 | hp2 | a0001 | c0001 | t0005 | g0148 | AMR | CLM | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | CLM | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | CLM | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | CLM | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG01433 | hp2 | a0001 | c0001 | t0006 | g0223 | AMR | CLM | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG01496 | hp1 | a0001 | c0001 | t0023 | g0140 | AMR | CLM | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG01496 | hp2 | a0001 | c0001 | t0011 | g0103 | AMR | CLM | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0077 | EUR | IBS | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0289 | EUR | IBS | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG01884 | hp1 | a0001 | c0001 | t0026 | g0184 | AFR | ACB | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG01884 | hp2 | a0001 | c0001 | t0018 | g0104 | AFR | ACB | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | ACB | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | ACB | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG01928 | hp1 | a0001 | c0001 | t0006 | g0229 | AMR | PEL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0023 | AMR | PEL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG01952 | hp1 | a0001 | c0001 | t0005 | g0151 | AMR | PEL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0024 | AMR | PEL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0045 | AMR | PEL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG01978 | hp2 | a0001 | c0001 | t0005 | g0145 | AMR | PEL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0020 | AMR | PEL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG01981 | hp2 | a0001 | c0001 | t0015 | g0014 | AMR | PEL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | KHV | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | KHV | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | ACB | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG02055 | hp2 | a0002 | c0003 | t0013 | g0194 | AFR | ACB | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | KHV | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG02074 | hp1 | a0001 | c0001 | t0005 | g0147 | EAS | KHV | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG02074 | hp2 | a0001 | c0001 | t0016 | g0067 | EAS | KHV | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | KHV | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | KHV | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | KHV | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | KHV | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | KHV | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | KHV | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG02145 | hp1 | a0001 | c0001 | t0006 | g0200 | AFR | ACB | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG02145 | hp2 | a0001 | c0002 | t0003 | g0089 | AFR | ACB | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0022 | AMR | PEL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG02148 | hp2 | a0001 | c0001 | t0005 | g0143 | AMR | PEL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | CDX | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | CDX | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | ACB | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG02257 | hp2 | a0001 | c0001 | t0003 | g0133 | AFR | ACB | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG02258 | hp1 | a0001 | c0001 | t0003 | g0093 | AFR | ACB | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0019 | AFR | ACB | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG02300 | hp1 | a0001 | c0001 | t0005 | g0141 | AMR | PEL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG02300 | hp2 | a0001 | c0004 | t0001 | g0242 | AMR | PEL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG02451 | hp1 | a0001 | c0001 | t0024 | g0154 | AFR | ACB | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG02451 | hp2 | a0001 | c0002 | t0001 | g0162 | AFR | ACB | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | GWD | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG02615 | hp1 | a0001 | c0001 | t0011 | g0105 | AFR | GWD | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | GWD | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | GWD | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | GWD | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG02630 | hp1 | a0001 | c0001 | t0006 | g0212 | AFR | GWD | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG02630 | hp2 | a0001 | c0001 | t0003 | g0112 | AFR | GWD | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG02647 | hp1 | a0001 | c0001 | t0012 | g0205 | AFR | GWD | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG02647 | hp2 | a0001 | c0002 | t0003 | g0088 | AFR | GWD | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG02683 | hp1 | a0001 | c0008 | t0001 | g0159 | SAS | PJL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG02683 | hp2 | a0001 | c0001 | t0005 | g0152 | SAS | PJL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG02698 | hp1 | a0001 | c0001 | t0005 | g0139 | SAS | PJL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG02717 | hp2 | a0001 | c0001 | t0003 | g0095 | AFR | GWD | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | GWD | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0288 | AFR | GWD | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0275 | SAS | PJL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG02735 | hp2 | a0001 | c0005 | t0005 | g0149 | SAS | PJL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0018 | SAS | PJL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0302 | AFR | GWD | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG02809 | hp2 | a0001 | c0001 | t0009 | g0155 | AFR | GWD | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | GWD | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG02886 | hp1 | a0001 | c0001 | t0003 | g0114 | AFR | GWD | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG02886 | hp2 | a0001 | c0002 | t0003 | g0094 | AFR | GWD | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | GWD | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG02895 | hp2 | a0001 | c0002 | t0001 | g0160 | AFR | GWD | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG02896 | hp1 | a0001 | c0001 | t0010 | g0083 | AFR | GWD | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | GWD | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG02897 | hp1 | a0001 | c0001 | t0010 | g0084 | AFR | GWD | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | GWD | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG02922 | hp1 | a0001 | c0002 | t0008 | g0137 | AFR | ESN | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG02922 | hp2 | a0001 | c0001 | t0011 | g0107 | AFR | ESN | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG02965 | hp1 | a0002 | c0003 | t0013 | g0189 | AFR | ESN | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG02965 | hp2 | a0001 | c0001 | t0003 | g0100 | AFR | ESN | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | ESN | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | ESN | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG02976 | hp1 | a0001 | c0001 | t0003 | g0117 | AFR | ESN | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | ESN | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG03017 | hp1 | a0001 | c0001 | t0003 | g0108 | SAS | PJL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG03017 | hp2 | a0001 | c0001 | t0006 | g0175 | SAS | PJL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG03041 | hp1 | a0001 | c0006 | t0003 | g0110 | AFR | GWD | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | GWD | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG03098 | hp1 | a0001 | c0001 | t0003 | g0090 | AFR | MSL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG03098 | hp2 | a0001 | c0001 | t0003 | g0115 | AFR | MSL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG03139 | hp1 | a0001 | c0001 | t0003 | g0102 | AFR | ESN | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | ESN | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG03195 | hp1 | a0001 | c0001 | t0003 | g0091 | AFR | ESN | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG03195 | hp2 | a0001 | c0002 | t0001 | g0197 | AFR | ESN | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG03209 | hp1 | a0002 | c0003 | t0022 | g0109 | AFR | MSL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG03209 | hp2 | a0001 | c0002 | t0008 | g0136 | AFR | MSL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | MSL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG03225 | hp2 | a0002 | c0003 | t0019 | g0123 | AFR | MSL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG03239 | hp1 | a0001 | c0001 | t0006 | g0257 | SAS | PJL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0283 | SAS | PJL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | MSL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | MSL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0304 | AFR | GWD | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0280 | AFR | GWD | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0306 | AFR | MSL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | MSL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0047 | SAS | PJL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0271 | SAS | PJL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG03669 | hp1 | a0001 | c0001 | t0005 | g0142 | SAS | PJL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0282 | SAS | PJL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG03688 | hp1 | a0001 | c0001 | t0007 | g0038 | SAS | STU | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0273 | SAS | STU | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0238 | SAS | PJL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0258 | SAS | BEB | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0066 | SAS | BEB | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG03927 | hp1 | a0001 | c0004 | t0003 | g0118 | SAS | BEB | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0281 | SAS | BEB | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG04184 | hp1 | a0001 | c0001 | t0003 | g0132 | SAS | BEB | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG04184 | hp2 | a0001 | c0001 | t0003 | g0113 | SAS | BEB | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0207 | SAS | STU | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0069 | SAS | STU | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA18522 | hp1 | a0001 | c0001 | t0003 | g0092 | AFR | YRI | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA18522 | hp2 | a0001 | c0001 | t0008 | g0134 | AFR | YRI | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA18612 | hp1 | a0001 | c0001 | t0003 | g0116 | EAS | CHB | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | CHB | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | CHB | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA18747 | hp2 | a0001 | c0001 | t0003 | g0121 | EAS | CHB | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA18906 | hp1 | a0001 | c0001 | t0008 | g0135 | AFR | YRI | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA18906 | hp2 | a0001 | c0001 | t0009 | g0153 | AFR | YRI | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA18941 | hp1 | a0001 | c0001 | t0003 | g0126 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA18943 | hp1 | a0001 | c0001 | t0004 | g0255 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA18945 | hp2 | a0001 | c0001 | t0004 | g0256 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA18947 | hp2 | a0001 | c0001 | t0004 | g0169 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA18949 | hp1 | a0001 | c0001 | t0007 | g0051 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA18951 | hp2 | a0001 | c0001 | t0003 | g0097 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA18952 | hp1 | a0001 | c0001 | t0005 | g0144 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA18957 | hp1 | a0001 | c0001 | t0007 | g0073 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA18960 | hp2 | a0001 | c0001 | t0007 | g0048 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA18962 | hp1 | a0001 | c0001 | t0004 | g0170 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA18962 | hp2 | a0004 | c0007 | t0002 | g0042 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA18963 | hp2 | a0001 | c0001 | t0004 | g0286 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA18964 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA18964 | hp2 | a0001 | c0001 | t0007 | g0034 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA18965 | hp2 | a0001 | c0001 | t0004 | g0293 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA18971 | hp1 | a0001 | c0001 | t0003 | g0124 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA18974 | hp1 | a0001 | c0001 | t0004 | g0305 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA18975 | hp2 | a0001 | c0001 | t0003 | g0099 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA18977 | hp1 | a0001 | c0001 | t0006 | g0265 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA18981 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA18981 | hp2 | a0001 | c0001 | t0003 | g0122 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA18983 | hp1 | a0001 | c0001 | t0003 | g0130 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA18983 | hp2 | a0001 | c0001 | t0003 | g0120 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA18984 | hp1 | a0001 | c0001 | t0007 | g0071 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA18984 | hp2 | a0001 | c0001 | t0004 | g0296 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA18986 | hp1 | a0001 | c0001 | t0005 | g0150 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA18986 | hp2 | a0001 | c0001 | t0004 | g0168 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA18988 | hp1 | a0001 | c0001 | t0007 | g0074 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA18991 | hp1 | a0001 | c0001 | t0004 | g0165 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA18991 | hp2 | a0001 | c0001 | t0006 | g0268 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA18995 | hp1 | a0001 | c0001 | t0004 | g0167 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA19000 | hp2 | a0001 | c0001 | t0003 | g0131 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA19001 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA19001 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA19002 | hp2 | a0001 | c0001 | t0004 | g0235 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA19006 | hp2 | a0001 | c0001 | t0003 | g0125 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA19011 | hp2 | a0001 | c0001 | t0004 | g0259 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA19012 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA19012 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA19030 | hp1 | a0001 | c0001 | t0010 | g0086 | AFR | LWK | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | LWK | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA19043 | hp1 | a0001 | c0001 | t0003 | g0101 | AFR | LWK | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA19043 | hp2 | a0001 | c0001 | t0017 | g0085 | AFR | LWK | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA19057 | hp1 | a0001 | c0001 | t0003 | g0129 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA19057 | hp2 | a0001 | c0001 | t0004 | g0166 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA19060 | hp2 | a0001 | c0001 | t0004 | g0298 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA19064 | hp1 | a0001 | c0001 | t0004 | g0158 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA19067 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA19067 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA19074 | hp2 | a0001 | c0001 | t0020 | g0128 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA19075 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA19082 | hp2 | a0001 | c0001 | t0003 | g0098 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA19083 | hp2 | a0001 | c0001 | t0007 | g0065 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA19084 | hp1 | a0001 | c0001 | t0003 | g0096 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA19087 | hp1 | a0001 | c0001 | t0004 | g0276 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA19090 | hp2 | a0001 | c0001 | t0006 | g0240 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | YRI | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | YRI | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA20129 | hp1 | a0001 | c0001 | t0012 | g0220 | AFR | ASW | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | ASW | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0015 | EUR | TSI | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0300 | EUR | TSI | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0225 | SAS | GIH | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0032 | SAS | GIH | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | ACB | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0046 | AFR | ACB | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG02559 | hp1 | a0001 | c0001 | t0009 | g0156 | AFR | ACB | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG02559 | hp2 | a0001 | c0005 | t0005 | g0146 | AFR | ACB | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG03471 | hp1 | a0001 | c0001 | t0021 | g0106 | AFR | MSL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | MSL | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0025 | AFR | USA | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
HG06807 | hp2 | a0001 | c0001 | t0009 | g0157 | AFR | USA | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA18955 | hp1 | a0001 | c0001 | t0005 | g0138 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0206 | REF | REF | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0272 | REF | REF | HTR4_chr5_148476547_148659527 | HTR4 | chr5 | 148476547 | 148659527 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:148483255 | C | T | 1 | a0002 | 4 | HG02055.hp2 HG02965.hp1 HG03209.hp1 others(1): Show |
missense_variant | MODERATE | c.1115G>A | p.Cys372Tyr | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 7/7 | 1628/3336 | 1115/1167 | 372/388 | chr5 | 148483255 | |||
chr5:148483280 | A | G | 1 | a0004 | 1 | NA18962.hp2 | missense_variant | MODERATE | c.1090T>C | p.Cys364Arg | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 7/7 | 1603/3336 | 1090/1167 | 364/388 | chr5 | 148483280 | |||
chr5:148550218 | G | A | 1 | a0003 | 1 | HG01243.hp1 | missense_variant | MODERATE | c.71C>T | p.Thr24Met | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 3/7 | 584/3336 | 71/1167 | 24/388 | chr5 | 148550218 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:148509464 | A | G | 1 | a0001c0002 | 8 | HG02145.hp2 HG02451.hp2 HG02647.hp2 others(5): Show |
synonymous_variant | LOW | c.1068T>C | p.His356His | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/7 | 1581/3336 | 1068/1167 | 356/388 | chr5 | 148509464 | |||
chr5:148509548 | G | A | 1 | a0001c0006 | 1 | HG03041.hp1 | synonymous_variant | LOW | c.984C>T | p.Cys328Cys | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/7 | 1497/3336 | 984/1167 | 328/388 | chr5 | 148509548 | |||
chr5:148509590 | G | A | 1 | a0001c0008 | 1 | HG02683.hp1 | synonymous_variant | LOW | c.942C>T | p.Phe314Phe | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/7 | 1455/3336 | 942/1167 | 314/388 | chr5 | 148509590 | |||
chr5:148509785 | A | G | 3 | a0001c0004 a0001c0006 a0003c0009 |
4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
synonymous_variant | LOW | c.747T>C | p.His249His | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/7 | 1260/3336 | 747/1167 | 249/388 | chr5 | 148509785 | |||
chr5:148550177 | G | A | 1 | a0001c0005 | 2 | HG02559.hp2 HG02735.hp2 |
synonymous_variant | LOW | c.112C>T | p.Leu38Leu | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 3/7 | 625/3336 | 112/1167 | 38/388 | chr5 | 148550177 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:148481738 | A | G | 1 | a0001c0001t0015 | 1 | HG01981.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1465T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 7/7 | 1465 | chr5 | 148481738 | ||||||
chr5:148482152 | G | T | 1 | a0001c0001t0025 | 1 | HG00099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1051C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 7/7 | 1051 | chr5 | 148482152 | ||||||
chr5:148482193 | G | C | 6 | a0001c0001t0006 a0001c0001t0007 a0001c0001t0011 others(3): Show |
25 | HG00438.hp1 HG00544.hp2 HG01257.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1010C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 7/7 | 1010 | chr5 | 148482193 | ||||||
chr5:148482204 | G | A | 3 | a0002c0003t0013 a0002c0003t0019 a0002c0003t0022 |
4 | HG02055.hp2 HG02965.hp1 HG03209.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*999C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 7/7 | 999 | chr5 | 148482204 | ||||||
chr5:148482404 | T | C | 3 | a0001c0001t0004 a0001c0001t0016 a0001c0001t0020 |
22 | HG00544.hp1 HG02074.hp2 NA18943.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*799A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 7/7 | 799 | chr5 | 148482404 | ||||||
chr5:148482442 | A | G | 3 | a0001c0001t0012 a0001c0001t0017 a0001c0001t0018 |
4 | HG01884.hp2 HG02647.hp1 NA19043.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*761T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 7/7 | 761 | chr5 | 148482442 | ||||||
chr5:148482609 | C | G | 1 | a0001c0001t0024 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*594G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 7/7 | 594 | chr5 | 148482609 | ||||||
chr5:148482724 | G | A | 1 | a0001c0001t0021 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*479C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 7/7 | 479 | chr5 | 148482724 | ||||||
chr5:148483072 | C | A | 1 | a0001c0001t0026 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*131G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 7/7 | 131 | chr5 | 148483072 | ||||||
chr5:148483098 | G | A | 1 | a0002c0003t0022 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*105C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 7/7 | 105 | chr5 | 148483098 | ||||||
chr5:148654084 | G | A | 2 | a0001c0001t0008 a0001c0002t0008 |
4 | HG02922.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-70C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/7 | chr5 | 148654084 | |||||||
chr5:148654188 | G | C | 1 | a0001c0001t0014 | 1 | HG00438.hp1 | 5_prime_UTR_variant | MODIFIER | c.-174C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/7 | 17174 | chr5 | 148654188 | ||||||
chr5:148654296 | C | T | 2 | a0001c0001t0009 a0001c0001t0024 |
5 | HG02451.hp1 HG02559.hp1 HG02809.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-282G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/7 | 17282 | chr5 | 148654296 | ||||||
chr5:148654328 | C | T | 3 | a0001c0001t0005 a0001c0001t0023 a0001c0005t0005 |
17 | HG01071.hp1 HG01074.hp2 HG01257.hp2 others(14): Show |
5_prime_UTR_variant | MODIFIER | c.-314G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/7 | 17314 | chr5 | 148654328 | ||||||
chr5:148654421 | C | G | 2 | a0001c0001t0010 a0001c0001t0017 |
4 | HG02896.hp1 HG02897.hp1 NA19030.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-407G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/7 | 17407 | chr5 | 148654421 | ||||||
chr5:148654434 | G | A | 1 | a0003c0009t0027 | 1 | HG01243.hp1 | 5_prime_UTR_variant | MODIFIER | c.-420C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/7 | 17420 | chr5 | 148654434 | ||||||
chr5:148654450 | A | G | 20 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0007 others(17): Show |
134 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(131): Show |
5_prime_UTR_variant | MODIFIER | c.-436T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/7 | 17436 | chr5 | 148654450 | ||||||
chr5:148654477 | C | G | 5 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0015 others(2): Show |
78 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(75): Show |
5_prime_UTR_variant | MODIFIER | c.-463G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/7 | 17463 | chr5 | 148654477 | ||||||
chr5:148654482 | C | G | 1 | a0001c0001t0014 | 1 | HG00438.hp1 | 5_prime_UTR_variant | MODIFIER | c.-468G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/7 | 17468 | chr5 | 148654482 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:148483471 | A | G | 101 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0173 others(98): Show |
103 | HG00438.hp1 HG00544.hp1 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.1077-178T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148483471 | |||||||
chr5:148483523 | T | A | 2 | a0001c0001t0001g0291 a0001c0001t0005g0001 |
3 | HG01071.hp1 HG01074.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1077-230A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148483523 | |||||||
chr5:148483536 | C | T | 1 | a0002c0003t0019g0123 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1077-243G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148483536 | |||||||
chr5:148483555 | C | T | 4 | a0001c0001t0012g0205 a0001c0001t0012g0220 a0001c0001t0017g0085 others(1): Show |
4 | HG01884.hp2 HG02647.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1077-262G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148483555 | |||||||
chr5:148483797 | T | C | 3 | a0001c0001t0001g0173 a0001c0001t0001g0190 a0001c0001t0001g0191 |
3 | HG01891.hp1 HG02818.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1077-504A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148483797 | |||||||
chr5:148483934 | ATTAT | A | 214 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0171 others(211): Show |
215 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.1077-645_1077-642d others(6): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148483934 | |||||||
chr5:148483934 | ATTATTTA others(1): Show |
A | 26 | a0001c0001t0001g0161 a0001c0001t0001g0183 a0001c0001t0001g0185 others(23): Show |
26 | HG00099.hp2 HG01243.hp1 HG02148.hp1 others(23): Show |
intron_variant | MODIFIER | c.1077-649_1077-642d others(10): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148483934 | |||||||
chr5:148483934 | ATTATTTA others(5): Show |
A | 20 | a0001c0001t0001g0003 a0001c0001t0001g0211 a0001c0001t0001g0213 others(17): Show |
21 | HG01069.hp2 HG01071.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.1077-653_1077-642d others(14): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148483934 | |||||||
chr5:148483934 | ATTATTTA others(9): Show |
A | 4 | a0001c0001t0001g0210 a0001c0001t0001g0214 a0001c0001t0001g0215 others(1): Show |
4 | HG01167.hp2 HG01169.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1077-657_1077-642d others(18): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148483934 | |||||||
chr5:148483934 | ATTATTTA others(17): Show |
A | 25 | a0001c0001t0004g0002 a0001c0001t0004g0158 a0001c0001t0004g0165 others(22): Show |
26 | HG00544.hp1 HG02055.hp2 HG02074.hp2 others(23): Show |
intron_variant | MODIFIER | c.1077-665_1077-642d others(26): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148483934 | |||||||
chr5:148484023 | G | A | 1 | a0001c0001t0001g0204 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1077-730C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148484023 | |||||||
chr5:148484091 | G | T | 1 | a0001c0001t0014g0004 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1077-798C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148484091 | |||||||
chr5:148484234 | A | G | 1 | a0001c0001t0001g0181 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1077-941T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148484234 | |||||||
chr5:148484271 | C | T | 3 | a0001c0001t0001g0232 a0001c0001t0001g0250 a0001c0001t0003g0125 |
3 | NA18974.hp2 NA19006.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1077-978G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148484271 | |||||||
chr5:148484289 | T | C | 3 | a0001c0001t0001g0003 a0001c0001t0001g0246 a0001c0001t0001g0247 |
4 | HG01069.hp2 HG01071.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1077-996A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148484289 | |||||||
chr5:148484320 | G | A | 1 | a0001c0001t0016g0067 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1077-1027C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148484320 | |||||||
chr5:148484415 | A | G | 1 | a0001c0001t0004g0305 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1077-1122T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148484415 | |||||||
chr5:148484547 | T | A | 21 | a0001c0001t0004g0002 a0001c0001t0004g0158 a0001c0001t0004g0165 others(18): Show |
22 | HG00544.hp1 HG02074.hp2 NA18943.hp1 others(19): Show |
intron_variant | MODIFIER | c.1077-1254A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148484547 | |||||||
chr5:148484603 | T | C | 21 | a0001c0001t0004g0002 a0001c0001t0004g0158 a0001c0001t0004g0165 others(18): Show |
22 | HG00544.hp1 HG02074.hp2 NA18943.hp1 others(19): Show |
intron_variant | MODIFIER | c.1077-1310A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148484603 | |||||||
chr5:148484609 | C | G | 1 | a0001c0001t0003g0127 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1077-1316G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148484609 | |||||||
chr5:148484842 | C | G | 1 | a0001c0002t0008g0137 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1077-1549G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148484842 | |||||||
chr5:148484873 | C | G | 1 | a0001c0001t0010g0086 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1077-1580G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148484873 | |||||||
chr5:148485074 | G | A | 3 | a0001c0001t0005g0141 a0001c0001t0005g0143 a0001c0001t0005g0151 |
3 | HG01952.hp1 HG02148.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.1077-1781C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148485074 | |||||||
chr5:148485496 | G | C | 130 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0172 others(127): Show |
131 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.1077-2203C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148485496 | |||||||
chr5:148485527 | G | C | 2 | a0001c0001t0002g0077 a0001c0001t0005g0145 |
2 | HG01516.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.1077-2234C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148485527 | |||||||
chr5:148485565 | C | T | 16 | a0001c0001t0001g0264 a0001c0001t0002g0057 a0001c0001t0002g0058 others(13): Show |
17 | HG01952.hp1 HG02148.hp2 HG02300.hp1 others(14): Show |
intron_variant | MODIFIER | c.1077-2272G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148485565 | |||||||
chr5:148485947 | G | T | 1 | a0001c0001t0001g0301 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1077-2654C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148485947 | |||||||
chr5:148486127 | C | G | 1 | a0001c0001t0002g0035 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1077-2834G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148486127 | |||||||
chr5:148486129 | C | T | 1 | a0001c0001t0001g0269 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1077-2836G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148486129 | |||||||
chr5:148486142 | G | A | 1 | a0001c0001t0010g0086 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1077-2849C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148486142 | |||||||
chr5:148486319 | T | G | 105 | a0001c0001t0001g0161 a0001c0001t0001g0183 a0001c0001t0001g0185 others(102): Show |
105 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.1077-3026A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148486319 | |||||||
chr5:148486339 | C | T | 7 | a0001c0001t0002g0005 a0001c0001t0002g0036 a0001c0001t0003g0120 others(4): Show |
7 | HG02080.hp1 NA18941.hp1 NA18981.hp2 others(4): Show |
intron_variant | MODIFIER | c.1077-3046G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148486339 | |||||||
chr5:148486393 | G | A | 1 | a0001c0001t0002g0069 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1077-3100C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148486393 | |||||||
chr5:148486437 | C | A | 1 | a0001c0001t0010g0086 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1077-3144G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148486437 | |||||||
chr5:148486442 | A | G | 3 | a0001c0001t0001g0281 a0001c0001t0001g0282 a0001c0001t0001g0283 |
3 | HG03239.hp2 HG03669.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1077-3149T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148486442 | |||||||
chr5:148486483 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1077-3190C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148486483 | |||||||
chr5:148486692 | C | A | 1 | a0002c0003t0013g0194 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1077-3399G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148486692 | |||||||
chr5:148486781 | T | C | 1 | a0001c0006t0003g0110 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1077-3488A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148486781 | |||||||
chr5:148486926 | C | T | 1 | a0001c0001t0003g0113 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1077-3633G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148486926 | |||||||
chr5:148487102 | CT | C | 171 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0177 others(168): Show |
173 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.1077-3810delA | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148487102 | |||||||
chr5:148487144 | G | C | 1 | a0001c0001t0001g0176 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1077-3851C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148487144 | |||||||
chr5:148487168 | GTT | G | 3 | a0001c0001t0003g0095 a0001c0001t0009g0155 a0001c0001t0012g0220 |
3 | HG02717.hp2 HG02809.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1077-3877_1077-387 others(6): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148487168 | |||||||
chr5:148487215 | G | A | 4 | a0001c0001t0001g0266 a0001c0001t0001g0277 a0001c0001t0004g0255 others(1): Show |
4 | NA18943.hp1 NA18945.hp2 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.1077-3922C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148487215 | |||||||
chr5:148487232 | T | A | 1 | a0001c0001t0021g0106 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1077-3939A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148487232 | |||||||
chr5:148487239 | A | T | 1 | a0001c0001t0001g0280 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1077-3946T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148487239 | |||||||
chr5:148487347 | G | C | 1 | a0001c0001t0001g0243 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1077-4054C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148487347 | |||||||
chr5:148487391 | A | G | 2 | a0001c0001t0001g0238 a0001c0001t0006g0175 |
2 | HG03017.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1077-4098T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148487391 | |||||||
chr5:148487576 | C | G | 172 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0177 others(169): Show |
174 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.1077-4283G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148487576 | |||||||
chr5:148487673 | C | CAGAGAGT others(53): Show |
1 | a0001c0001t0021g0106 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1077-4381_1077-438 others(64): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148487673 | |||||||
chr5:148487673 | CAGAGAGC others(23): Show |
C | 2 | a0001c0004t0001g0242 a0001c0004t0003g0118 |
2 | HG02300.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1077-4410_1077-438 others(34): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148487673 | |||||||
chr5:148487916 | G | T | 165 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0177 others(162): Show |
167 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.1077-4623C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148487916 | |||||||
chr5:148487974 | G | T | 5 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0216 others(2): Show |
5 | HG01167.hp1 HG01884.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1077-4681C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148487974 | |||||||
chr5:148488206 | T | A | 1 | a0001c0006t0003g0110 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1077-4913A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148488206 | |||||||
chr5:148488221 | T | C | 2 | a0001c0004t0001g0242 a0001c0004t0003g0118 |
2 | HG02300.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1077-4928A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148488221 | |||||||
chr5:148488284 | G | T | 60 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0177 others(57): Show |
62 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.1077-4991C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148488284 | |||||||
chr5:148488375 | G | A | 60 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0177 others(57): Show |
62 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.1077-5082C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148488375 | |||||||
chr5:148488461 | T | C | 1 | a0001c0001t0010g0086 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1077-5168A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148488461 | |||||||
chr5:148488464 | T | C | 5 | a0001c0001t0002g0007 a0001c0001t0003g0096 a0001c0001t0003g0097 others(2): Show |
5 | HG00423.hp2 HG00544.hp2 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.1077-5171A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148488464 | |||||||
chr5:148488539 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1077-5246G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148488539 | |||||||
chr5:148488573 | A | G | 102 | a0001c0001t0001g0161 a0001c0001t0001g0185 a0001c0001t0001g0188 others(99): Show |
102 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.1077-5280T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148488573 | |||||||
chr5:148488592 | G | A | 2 | a0001c0004t0001g0242 a0001c0004t0003g0118 |
2 | HG02300.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1077-5299C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148488592 | |||||||
chr5:148488693 | G | A | 6 | a0001c0001t0002g0027 a0001c0001t0002g0052 a0001c0001t0003g0087 others(3): Show |
6 | HG00673.hp1 HG02074.hp1 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.1077-5400C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148488693 | |||||||
chr5:148488824 | C | A | 2 | a0001c0001t0001g0249 a0001c0001t0001g0254 |
2 | NA18971.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.1077-5531G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148488824 | |||||||
chr5:148488853 | C | G | 4 | a0001c0001t0002g0027 a0001c0001t0002g0052 a0001c0001t0003g0087 others(1): Show |
4 | HG00673.hp1 HG02074.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.1077-5560G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148488853 | |||||||
chr5:148488856 | A | C | 1 | a0001c0001t0003g0112 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1077-5563T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148488856 | |||||||
chr5:148488902 | T | C | 2 | a0001c0004t0001g0242 a0001c0004t0003g0118 |
2 | HG02300.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1077-5609A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148488902 | |||||||
chr5:148488950 | G | A | 15 | a0001c0001t0001g0185 a0001c0001t0001g0188 a0001c0001t0001g0193 others(12): Show |
15 | HG01069.hp2 HG01071.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.1077-5657C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148488950 | |||||||
chr5:148488979 | C | T | 1 | a0003c0009t0027g0307 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1077-5686G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148488979 | |||||||
chr5:148489008 | CAG | C | 9 | a0001c0001t0001g0192 a0001c0001t0001g0251 a0001c0001t0001g0252 others(6): Show |
9 | HG01884.hp2 HG02615.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1077-5717_1077-571 others(6): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148489008 | |||||||
chr5:148489056 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1077-5763C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148489056 | |||||||
chr5:148489276 | A | G | 1 | a0001c0001t0010g0086 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1077-5983T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148489276 | |||||||
chr5:148489308 | A | T | 101 | a0001c0001t0001g0161 a0001c0001t0001g0185 a0001c0001t0001g0188 others(98): Show |
101 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.1077-6015T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148489308 | |||||||
chr5:148489380 | A | G | 1 | a0001c0006t0003g0110 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1077-6087T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148489380 | |||||||
chr5:148489432 | G | T | 6 | a0001c0001t0002g0027 a0001c0001t0002g0052 a0001c0001t0003g0087 others(3): Show |
6 | HG00673.hp1 HG02074.hp1 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.1077-6139C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148489432 | |||||||
chr5:148489557 | T | C | 1 | a0001c0001t0001g0186 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1077-6264A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148489557 | |||||||
chr5:148489845 | C | T | 65 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0177 others(62): Show |
67 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.1077-6552G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148489845 | |||||||
chr5:148489846 | T | G | 67 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0177 others(64): Show |
69 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.1077-6553A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148489846 | |||||||
chr5:148489946 | A | G | 2 | a0001c0004t0001g0242 a0001c0004t0003g0118 |
2 | HG02300.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1077-6653T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148489946 | |||||||
chr5:148490146 | T | TATGTATA | 7 | a0001c0001t0001g0183 a0001c0001t0001g0195 a0001c0001t0001g0196 others(4): Show |
7 | HG02257.hp1 HG02451.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1077-6854_1077-685 others(11): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148490146 | |||||||
chr5:148490317 | C | T | 1 | a0001c0001t0026g0184 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1077-7024G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148490317 | |||||||
chr5:148490413 | G | A | 2 | a0001c0001t0001g0186 a0001c0001t0001g0287 |
2 | HG01167.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1077-7120C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148490413 | |||||||
chr5:148490433 | T | C | 61 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0177 others(58): Show |
63 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.1077-7140A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148490433 | |||||||
chr5:148490514 | A | T | 1 | a0001c0001t0026g0184 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1077-7221T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148490514 | |||||||
chr5:148490528 | C | T | 1 | a0001c0001t0002g0021 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1077-7235G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148490528 | |||||||
chr5:148490554 | G | T | 1 | a0001c0001t0001g0225 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1077-7261C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148490554 | |||||||
chr5:148490946 | G | T | 1 | a0001c0001t0003g0099 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1077-7653C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148490946 | |||||||
chr5:148491201 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1077-7908C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148491201 | |||||||
chr5:148491249 | C | T | 2 | a0001c0001t0004g0255 a0001c0001t0004g0256 |
2 | NA18943.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.1077-7956G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148491249 | |||||||
chr5:148491317 | T | TA | 4 | a0001c0001t0002g0027 a0001c0001t0002g0052 a0001c0001t0003g0087 others(1): Show |
4 | HG00673.hp1 HG02074.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.1077-8025dupT | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148491317 | |||||||
chr5:148491319 | T | A | 2 | a0001c0004t0001g0242 a0001c0004t0003g0118 |
2 | HG02300.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1077-8026A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148491319 | |||||||
chr5:148491320 | A | T | 6 | a0001c0001t0002g0027 a0001c0001t0002g0052 a0001c0001t0003g0087 others(3): Show |
6 | HG00673.hp1 HG02074.hp1 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.1077-8027T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148491320 | |||||||
chr5:148491322 | A | T | 6 | a0001c0001t0002g0027 a0001c0001t0002g0052 a0001c0001t0003g0087 others(3): Show |
6 | HG00673.hp1 HG02074.hp1 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.1077-8029T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148491322 | |||||||
chr5:148491324 | T | A | 71 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0177 others(68): Show |
73 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.1077-8031A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148491324 | |||||||
chr5:148491326 | T | A | 69 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0177 others(66): Show |
71 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.1077-8033A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148491326 | |||||||
chr5:148491328 | T | A | 63 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(60): Show |
64 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.1077-8035A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148491328 | |||||||
chr5:148491355 | A | G | 2 | a0001c0004t0001g0242 a0001c0004t0003g0118 |
2 | HG02300.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1077-8062T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148491355 | |||||||
chr5:148491574 | G | A | 162 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0173 others(159): Show |
164 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.1077-8281C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148491574 | |||||||
chr5:148491576 | C | A | 162 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0173 others(159): Show |
164 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.1077-8283G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148491576 | |||||||
chr5:148491636 | A | T | 164 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0173 others(161): Show |
166 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.1077-8343T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148491636 | |||||||
chr5:148491656 | C | T | 69 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0177 others(66): Show |
71 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.1077-8363G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148491656 | |||||||
chr5:148491828 | A | G | 1 | a0003c0009t0027g0307 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1077-8535T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148491828 | |||||||
chr5:148491856 | C | T | 1 | a0001c0001t0003g0100 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1077-8563G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148491856 | |||||||
chr5:148491911 | C | T | 2 | a0001c0001t0001g0250 a0001c0001t0002g0019 |
2 | HG02258.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.1077-8618G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148491911 | |||||||
chr5:148491927 | A | T | 1 | a0001c0001t0001g0250 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1077-8634T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148491927 | |||||||
chr5:148491945 | A | G | 161 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0173 others(158): Show |
163 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.1077-8652T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148491945 | |||||||
chr5:148491948 | A | G | 1 | a0001c0001t0006g0200 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1077-8655T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148491948 | |||||||
chr5:148492144 | C | T | 4 | a0001c0001t0001g0209 a0001c0001t0001g0285 a0001c0001t0002g0078 others(1): Show |
4 | NA18945.hp1 NA18949.hp2 NA18952.hp2 others(1): Show |
intron_variant | MODIFIER | c.1077-8851G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148492144 | |||||||
chr5:148492176 | C | T | 65 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(62): Show |
66 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.1077-8883G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148492176 | |||||||
chr5:148492187 | C | A | 1 | a0001c0001t0007g0073 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1077-8894G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148492187 | |||||||
chr5:148492243 | A | G | 63 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(60): Show |
64 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.1077-8950T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148492243 | |||||||
chr5:148492357 | T | C | 12 | a0001c0001t0001g0202 a0001c0001t0001g0211 a0001c0001t0001g0213 others(9): Show |
12 | HG01243.hp2 HG02055.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.1077-9064A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148492357 | |||||||
chr5:148492403 | G | A | 161 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0173 others(158): Show |
163 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.1077-9110C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148492403 | |||||||
chr5:148492533 | G | A | 6 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0190 others(3): Show |
7 | HG01074.hp1 HG01891.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1077-9240C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148492533 | |||||||
chr5:148492591 | T | G | 5 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0216 others(2): Show |
5 | HG01167.hp1 HG01884.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1077-9298A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148492591 | |||||||
chr5:148492849 | C | T | 3 | a0001c0001t0003g0095 a0001c0001t0009g0155 a0001c0001t0012g0220 |
3 | HG02717.hp2 HG02809.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1077-9556G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148492849 | |||||||
chr5:148492902 | G | A | 161 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0173 others(158): Show |
163 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.1077-9609C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148492902 | |||||||
chr5:148493003 | G | T | 161 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0173 others(158): Show |
163 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.1077-9710C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148493003 | |||||||
chr5:148493046 | G | C | 2 | a0001c0004t0001g0242 a0001c0004t0003g0118 |
2 | HG02300.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1077-9753C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148493046 | |||||||
chr5:148493350 | G | A | 1 | a0001c0001t0002g0022 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1077-10057C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148493350 | |||||||
chr5:148493659 | C | T | 1 | a0001c0001t0005g0144 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1077-10366G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148493659 | |||||||
chr5:148493751 | G | T | 1 | a0001c0001t0001g0203 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1077-10458C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148493751 | |||||||
chr5:148493796 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1077-10503C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148493796 | |||||||
chr5:148493831 | C | T | 1 | a0001c0001t0010g0086 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1077-10538G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148493831 | |||||||
chr5:148493834 | T | C | 161 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0173 others(158): Show |
163 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.1077-10541A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148493834 | |||||||
chr5:148493941 | T | C | 2 | a0001c0001t0001g0253 a0001c0001t0005g0138 |
2 | HG02027.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.1077-10648A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148493941 | |||||||
chr5:148494097 | A | G | 1 | a0001c0001t0001g0248 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1077-10804T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148494097 | |||||||
chr5:148494150 | T | A | 1 | a0001c0001t0001g0239 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1077-10857A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148494150 | |||||||
chr5:148494187 | T | C | 166 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0173 others(163): Show |
168 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.1077-10894A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148494187 | |||||||
chr5:148494206 | G | A | 6 | a0001c0001t0001g0271 a0001c0001t0002g0015 a0001c0001t0002g0016 others(3): Show |
6 | HG00099.hp2 HG00323.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.1077-10913C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148494206 | |||||||
chr5:148494270 | G | A | 1 | a0001c0001t0006g0229 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1077-10977C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148494270 | |||||||
chr5:148494989 | G | C | 1 | a0003c0009t0027g0307 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1077-11696C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148494989 | |||||||
chr5:148494993 | G | A | 161 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0173 others(158): Show |
163 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.1077-11700C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148494993 | |||||||
chr5:148495056 | A | G | 2 | a0001c0004t0001g0242 a0001c0004t0003g0118 |
2 | HG02300.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1077-11763T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148495056 | |||||||
chr5:148495125 | G | A | 175 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0173 others(172): Show |
177 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.1077-11832C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148495125 | |||||||
chr5:148495160 | T | A | 1 | a0001c0001t0001g0243 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1077-11867A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148495160 | |||||||
chr5:148495297 | A | G | 6 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0216 others(3): Show |
6 | HG01167.hp1 HG01884.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1077-12004T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148495297 | |||||||
chr5:148495347 | G | T | 1 | a0001c0001t0001g0161 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1077-12054C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148495347 | |||||||
chr5:148495498 | C | T | 5 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0216 others(2): Show |
5 | HG01167.hp1 HG01884.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1077-12205G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148495498 | |||||||
chr5:148495518 | G | A | 92 | a0001c0001t0001g0161 a0001c0001t0001g0185 a0001c0001t0001g0188 others(89): Show |
92 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.1077-12225C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148495518 | |||||||
chr5:148495578 | G | A | 174 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0173 others(171): Show |
176 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.1077-12285C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148495578 | |||||||
chr5:148495706 | T | A | 1 | a0003c0009t0027g0307 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1077-12413A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148495706 | |||||||
chr5:148495907 | G | T | 1 | a0001c0002t0001g0197 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1077-12614C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148495907 | |||||||
chr5:148495912 | C | T | 3 | a0001c0001t0003g0095 a0001c0001t0009g0155 a0001c0001t0012g0220 |
3 | HG02717.hp2 HG02809.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1077-12619G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148495912 | |||||||
chr5:148496026 | G | A | 2 | a0001c0002t0001g0197 a0001c0002t0003g0088 |
2 | HG02647.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1077-12733C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148496026 | |||||||
chr5:148496049 | G | T | 2 | a0001c0001t0002g0081 a0001c0001t0002g0082 |
2 | NA18939.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.1077-12756C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148496049 | |||||||
chr5:148496188 | A | G | 100 | a0001c0001t0001g0161 a0001c0001t0001g0185 a0001c0001t0001g0188 others(97): Show |
100 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.1077-12895T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148496188 | |||||||
chr5:148496226 | C | T | 3 | a0001c0001t0002g0061 a0001c0001t0007g0051 a0001c0001t0007g0065 |
3 | NA18949.hp1 NA19075.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.1077-12933G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148496226 | |||||||
chr5:148496517 | A | G | 1 | a0001c0001t0001g0249 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1076+12939T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148496517 | |||||||
chr5:148496664 | T | C | 1 | a0001c0001t0003g0113 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1076+12792A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148496664 | |||||||
chr5:148496693 | G | C | 1 | a0001c0001t0017g0085 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1076+12763C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148496693 | |||||||
chr5:148496763 | G | A | 7 | a0001c0001t0001g0294 a0001c0001t0001g0295 a0001c0001t0003g0121 others(4): Show |
7 | HG00544.hp1 NA18747.hp2 NA18939.hp2 others(4): Show |
intron_variant | MODIFIER | c.1076+12693C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148496763 | |||||||
chr5:148496893 | G | A | 4 | a0001c0004t0001g0242 a0001c0004t0003g0118 a0001c0006t0003g0110 others(1): Show |
4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1076+12563C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148496893 | |||||||
chr5:148496926 | C | T | 10 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0190 others(7): Show |
11 | HG00673.hp1 HG01074.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.1076+12530G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148496926 | |||||||
chr5:148496948 | A | G | 4 | a0001c0001t0002g0027 a0001c0001t0002g0052 a0001c0001t0003g0087 others(1): Show |
4 | HG00673.hp1 HG02074.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.1076+12508T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148496948 | |||||||
chr5:148497126 | CA | C | 9 | a0001c0001t0001g0192 a0001c0001t0001g0251 a0001c0001t0001g0252 others(6): Show |
9 | HG01884.hp2 HG02615.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1076+12329delT | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148497126 | |||||||
chr5:148497137 | AT | A | 4 | a0001c0001t0002g0027 a0001c0001t0002g0052 a0001c0001t0003g0087 others(1): Show |
4 | HG00673.hp1 HG02074.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.1076+12318delA | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148497137 | |||||||
chr5:148497165 | T | C | 4 | a0001c0004t0001g0242 a0001c0004t0003g0118 a0001c0006t0003g0110 others(1): Show |
4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1076+12291A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148497165 | |||||||
chr5:148497288 | G | T | 1 | a0001c0001t0003g0099 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1076+12168C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148497288 | |||||||
chr5:148497421 | A | G | 1 | a0001c0006t0003g0110 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1076+12035T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148497421 | |||||||
chr5:148497562 | A | C | 1 | a0003c0009t0027g0307 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1076+11894T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148497562 | |||||||
chr5:148497753 | T | A | 5 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0216 others(2): Show |
5 | HG01167.hp1 HG01884.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1076+11703A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148497753 | |||||||
chr5:148497807 | C | A | 6 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0190 others(3): Show |
7 | HG01074.hp1 HG01891.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1076+11649G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148497807 | |||||||
chr5:148497887 | T | C | 22 | a0001c0001t0001g0202 a0001c0001t0001g0211 a0001c0001t0001g0213 others(19): Show |
22 | HG01243.hp2 HG01496.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.1076+11569A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148497887 | |||||||
chr5:148498013 | T | C | 4 | a0001c0001t0002g0027 a0001c0001t0002g0052 a0001c0001t0003g0087 others(1): Show |
4 | HG00673.hp1 HG02074.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.1076+11443A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148498013 | |||||||
chr5:148498092 | T | A | 2 | a0001c0001t0002g0053 a0001c0001t0002g0054 |
2 | NA18965.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.1076+11364A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148498092 | |||||||
chr5:148498118 | A | T | 1 | a0001c0001t0004g0158 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1076+11338T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148498118 | |||||||
chr5:148498161 | G | A | 165 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0173 others(162): Show |
167 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.1076+11295C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148498161 | |||||||
chr5:148498358 | T | C | 1 | a0001c0001t0002g0055 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1076+11098A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148498358 | |||||||
chr5:148498432 | C | T | 2 | a0001c0001t0001g0210 a0001c0001t0001g0290 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1076+11024G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148498432 | |||||||
chr5:148498462 | C | G | 8 | a0001c0002t0001g0160 a0001c0002t0001g0162 a0001c0002t0001g0197 others(5): Show |
8 | HG02145.hp2 HG02451.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1076+10994G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148498462 | |||||||
chr5:148498564 | C | T | 1 | a0001c0001t0003g0087 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1076+10892G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148498564 | |||||||
chr5:148498577 | C | G | 3 | a0001c0004t0001g0242 a0001c0004t0003g0118 a0003c0009t0027g0307 |
3 | HG01243.hp1 HG02300.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1076+10879G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148498577 | |||||||
chr5:148498643 | G | T | 4 | a0001c0004t0001g0242 a0001c0004t0003g0118 a0001c0006t0003g0110 others(1): Show |
4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1076+10813C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148498643 | |||||||
chr5:148498802 | C | T | 4 | a0001c0004t0001g0242 a0001c0004t0003g0118 a0001c0006t0003g0110 others(1): Show |
4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1076+10654G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148498802 | |||||||
chr5:148498970 | A | T | 1 | a0001c0001t0003g0111 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1076+10486T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148498970 | |||||||
chr5:148499029 | G | A | 4 | a0001c0001t0002g0027 a0001c0001t0002g0052 a0001c0001t0003g0087 others(1): Show |
4 | HG00673.hp1 HG02074.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.1076+10427C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148499029 | |||||||
chr5:148499109 | G | T | 4 | a0001c0004t0001g0242 a0001c0004t0003g0118 a0001c0006t0003g0110 others(1): Show |
4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1076+10347C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148499109 | |||||||
chr5:148499168 | T | C | 2 | a0001c0004t0001g0242 a0001c0004t0003g0118 |
2 | HG02300.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1076+10288A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148499168 | |||||||
chr5:148499212 | T | C | 5 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0190 others(2): Show |
6 | HG01891.hp1 HG02818.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1076+10244A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148499212 | |||||||
chr5:148499252 | A | T | 1 | a0001c0001t0002g0069 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1076+10204T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148499252 | |||||||
chr5:148499260 | A | G | 1 | a0001c0001t0021g0106 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1076+10196T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148499260 | |||||||
chr5:148499321 | G | T | 3 | a0001c0001t0004g0259 a0001c0001t0004g0276 a0001c0001t0006g0268 |
3 | NA18991.hp2 NA19011.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.1076+10135C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148499321 | |||||||
chr5:148499427 | A | AATTT | 4 | a0001c0004t0001g0242 a0001c0004t0003g0118 a0001c0006t0003g0110 others(1): Show |
4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1076+10025_1076+10 others(10): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148499427 | |||||||
chr5:148499711 | G | A | 165 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0173 others(162): Show |
167 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.1076+9745C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148499711 | |||||||
chr5:148499756 | G | T | 1 | a0001c0001t0001g0244 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1076+9700C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148499756 | |||||||
chr5:148499853 | A | C | 2 | a0001c0001t0001g0246 a0001c0001t0001g0247 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1076+9603T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148499853 | |||||||
chr5:148499893 | T | C | 62 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(59): Show |
63 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.1076+9563A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148499893 | |||||||
chr5:148500501 | C | A | 1 | a0001c0001t0021g0106 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1076+8955G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148500501 | |||||||
chr5:148500610 | A | G | 1 | a0001c0001t0021g0106 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1076+8846T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148500610 | |||||||
chr5:148500618 | A | G | 192 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0173 others(189): Show |
194 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.1076+8838T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148500618 | |||||||
chr5:148500919 | G | A | 4 | a0001c0004t0001g0242 a0001c0004t0003g0118 a0001c0006t0003g0110 others(1): Show |
4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1076+8537C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148500919 | |||||||
chr5:148500941 | T | C | 2 | a0001c0001t0002g0027 a0001c0001t0002g0052 |
2 | HG02135.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.1076+8515A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148500941 | |||||||
chr5:148501016 | T | C | 1 | a0001c0001t0001g0299 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1076+8440A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148501016 | |||||||
chr5:148501159 | T | C | 1 | a0001c0001t0003g0108 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1076+8297A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148501159 | |||||||
chr5:148501211 | C | T | 1 | a0001c0001t0001g0226 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1076+8245G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148501211 | |||||||
chr5:148501530 | G | A | 1 | a0001c0001t0001g0243 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1076+7926C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148501530 | |||||||
chr5:148501534 | A | G | 2 | a0001c0004t0001g0242 a0001c0004t0003g0118 |
2 | HG02300.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1076+7922T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148501534 | |||||||
chr5:148501688 | A | G | 92 | a0001c0001t0001g0161 a0001c0001t0001g0185 a0001c0001t0001g0188 others(89): Show |
92 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.1076+7768T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148501688 | |||||||
chr5:148501691 | A | C | 1 | a0001c0006t0003g0110 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1076+7765T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148501691 | |||||||
chr5:148501900 | A | G | 1 | a0001c0001t0003g0119 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1076+7556T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148501900 | |||||||
chr5:148501921 | A | T | 4 | a0001c0004t0001g0242 a0001c0004t0003g0118 a0001c0006t0003g0110 others(1): Show |
4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1076+7535T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148501921 | |||||||
chr5:148501989 | G | A | 1 | a0001c0001t0010g0086 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1076+7467C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148501989 | |||||||
chr5:148502388 | T | G | 4 | a0001c0004t0001g0242 a0001c0004t0003g0118 a0001c0006t0003g0110 others(1): Show |
4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1076+7068A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148502388 | |||||||
chr5:148502402 | C | T | 2 | a0001c0001t0001g0210 a0001c0001t0001g0290 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1076+7054G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148502402 | |||||||
chr5:148502468 | A | C | 4 | a0001c0004t0001g0242 a0001c0004t0003g0118 a0001c0006t0003g0110 others(1): Show |
4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1076+6988T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148502468 | |||||||
chr5:148502516 | A | AC | 4 | a0001c0004t0001g0242 a0001c0004t0003g0118 a0001c0006t0003g0110 others(1): Show |
4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1076+6939dupG | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148502516 | |||||||
chr5:148502566 | C | T | 100 | a0001c0001t0001g0161 a0001c0001t0001g0185 a0001c0001t0001g0188 others(97): Show |
100 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.1076+6890G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148502566 | |||||||
chr5:148502593 | TC | T | 4 | a0001c0001t0002g0027 a0001c0001t0002g0052 a0001c0001t0003g0087 others(1): Show |
4 | HG00673.hp1 HG02074.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.1076+6862delG | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148502593 | |||||||
chr5:148502907 | A | G | 1 | a0001c0001t0021g0106 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1076+6549T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148502907 | |||||||
chr5:148503006 | C | A | 1 | a0001c0006t0003g0110 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1076+6450G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148503006 | |||||||
chr5:148503220 | A | C | 4 | a0001c0001t0002g0027 a0001c0001t0002g0052 a0001c0001t0003g0087 others(1): Show |
4 | HG00673.hp1 HG02074.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.1076+6236T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148503220 | |||||||
chr5:148503313 | C | T | 1 | a0001c0001t0002g0062 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1076+6143G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148503313 | |||||||
chr5:148503315 | A | C | 1 | a0001c0001t0001g0288 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1076+6141T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148503315 | |||||||
chr5:148503319 | G | T | 4 | a0001c0004t0001g0242 a0001c0004t0003g0118 a0001c0006t0003g0110 others(1): Show |
4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1076+6137C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148503319 | |||||||
chr5:148503326 | G | A | 2 | a0001c0001t0002g0007 a0001c0001t0007g0006 |
2 | HG00423.hp2 HG00544.hp2 |
intron_variant | MODIFIER | c.1076+6130C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148503326 | |||||||
chr5:148503330 | C | G | 5 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0216 others(2): Show |
5 | HG01167.hp1 HG01884.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1076+6126G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148503330 | |||||||
chr5:148503332 | A | G | 1 | a0001c0001t0002g0047 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1076+6124T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148503332 | |||||||
chr5:148503512 | C | A | 4 | a0001c0004t0001g0242 a0001c0004t0003g0118 a0001c0006t0003g0110 others(1): Show |
4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1076+5944G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148503512 | |||||||
chr5:148503563 | G | T | 1 | a0001c0001t0001g0301 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1076+5893C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148503563 | |||||||
chr5:148503584 | C | T | 1 | a0001c0001t0002g0039 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1076+5872G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148503584 | |||||||
chr5:148503672 | G | T | 1 | a0001c0001t0024g0154 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1076+5784C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148503672 | |||||||
chr5:148503674 | G | A | 5 | a0001c0001t0003g0102 a0001c0001t0006g0212 a0001c0001t0011g0103 others(2): Show |
5 | HG01243.hp1 HG01496.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1076+5782C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148503674 | |||||||
chr5:148503731 | C | T | 174 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0177 others(171): Show |
176 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.1076+5725G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148503731 | |||||||
chr5:148503843 | C | G | 1 | a0001c0001t0003g0100 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1076+5613G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148503843 | |||||||
chr5:148503862 | A | G | 1 | a0001c0001t0010g0086 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1076+5594T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148503862 | |||||||
chr5:148503976 | G | A | 1 | a0001c0001t0001g0269 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1076+5480C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148503976 | |||||||
chr5:148504237 | G | T | 62 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(59): Show |
63 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.1076+5219C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148504237 | |||||||
chr5:148504389 | G | C | 1 | a0003c0009t0027g0307 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1076+5067C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148504389 | |||||||
chr5:148504487 | T | C | 1 | a0001c0001t0003g0095 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1076+4969A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148504487 | |||||||
chr5:148504570 | C | T | 7 | a0001c0001t0001g0183 a0001c0001t0001g0195 a0001c0001t0001g0196 others(4): Show |
7 | HG02257.hp1 HG02451.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1076+4886G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148504570 | |||||||
chr5:148504615 | C | T | 7 | a0001c0001t0001g0294 a0001c0001t0001g0295 a0001c0001t0003g0121 others(4): Show |
7 | HG00544.hp1 NA18747.hp2 NA18939.hp2 others(4): Show |
intron_variant | MODIFIER | c.1076+4841G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148504615 | |||||||
chr5:148504642 | T | C | 1 | a0001c0001t0021g0106 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1076+4814A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148504642 | |||||||
chr5:148504741 | C | G | 2 | a0001c0001t0001g0302 a0001c0001t0003g0117 |
2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1076+4715G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148504741 | |||||||
chr5:148504741 | C | T | 1 | a0001c0001t0003g0129 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1076+4715G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148504741 | |||||||
chr5:148504788 | G | A | 3 | a0001c0004t0001g0242 a0001c0004t0003g0118 a0003c0009t0027g0307 |
3 | HG01243.hp1 HG02300.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1076+4668C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148504788 | |||||||
chr5:148504792 | T | C | 36 | a0001c0001t0001g0163 a0001c0001t0001g0174 a0001c0001t0001g0176 others(33): Show |
36 | HG00323.hp2 HG00597.hp1 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.1076+4664A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148504792 | |||||||
chr5:148504820 | C | T | 4 | a0001c0004t0001g0242 a0001c0004t0003g0118 a0001c0006t0003g0110 others(1): Show |
4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1076+4636G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148504820 | |||||||
chr5:148504841 | T | G | 1 | a0003c0009t0027g0307 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1076+4615A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148504841 | |||||||
chr5:148504863 | C | T | 164 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0177 others(161): Show |
166 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.1076+4593G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148504863 | |||||||
chr5:148504871 | C | T | 1 | a0001c0001t0002g0069 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1076+4585G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148504871 | |||||||
chr5:148504872 | G | A | 1 | a0001c0001t0002g0081 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1076+4584C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148504872 | |||||||
chr5:148505048 | G | A | 1 | a0001c0005t0005g0146 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1076+4408C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148505048 | |||||||
chr5:148505105 | C | T | 164 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0177 others(161): Show |
166 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.1076+4351G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148505105 | |||||||
chr5:148505235 | C | T | 2 | a0001c0001t0001g0210 a0001c0001t0001g0290 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1076+4221G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148505235 | |||||||
chr5:148505417 | C | T | 4 | a0001c0001t0002g0027 a0001c0001t0002g0052 a0001c0001t0003g0087 others(1): Show |
4 | HG00673.hp1 HG02074.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.1076+4039G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148505417 | |||||||
chr5:148505427 | G | A | 4 | a0001c0001t0002g0027 a0001c0001t0002g0052 a0001c0001t0003g0087 others(1): Show |
4 | HG00673.hp1 HG02074.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.1076+4029C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148505427 | |||||||
chr5:148505496 | C | A | 1 | a0001c0001t0001g0003 | 2 | HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1076+3960G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148505496 | |||||||
chr5:148505505 | G | A | 1 | a0001c0001t0001g0003 | 2 | HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1076+3951C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148505505 | |||||||
chr5:148505540 | A | G | 4 | a0001c0004t0001g0242 a0001c0004t0003g0118 a0001c0006t0003g0110 others(1): Show |
4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1076+3916T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148505540 | |||||||
chr5:148505623 | C | T | 5 | a0001c0001t0001g0202 a0001c0001t0001g0218 a0001c0001t0001g0219 others(2): Show |
5 | HG01243.hp2 HG02572.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1076+3833G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148505623 | |||||||
chr5:148505628 | C | T | 7 | a0001c0002t0001g0160 a0001c0002t0001g0162 a0001c0002t0001g0197 others(4): Show |
7 | HG02145.hp2 HG02451.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1076+3828G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148505628 | |||||||
chr5:148505645 | T | C | 1 | a0001c0001t0001g0193 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1076+3811A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148505645 | |||||||
chr5:148505663 | A | G | 2 | a0001c0001t0002g0053 a0001c0001t0002g0054 |
2 | NA18965.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.1076+3793T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148505663 | |||||||
chr5:148505731 | A | T | 1 | a0001c0001t0001g0176 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1076+3725T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148505731 | |||||||
chr5:148505911 | A | G | 2 | a0001c0001t0001g0186 a0001c0001t0001g0287 |
2 | HG01167.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1076+3545T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148505911 | |||||||
chr5:148505929 | G | A | 1 | a0003c0009t0027g0307 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1076+3527C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148505929 | |||||||
chr5:148505930 | C | T | 1 | a0001c0001t0001g0284 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1076+3526G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148505930 | |||||||
chr5:148505953 | G | T | 1 | a0001c0006t0003g0110 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1076+3503C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148505953 | |||||||
chr5:148505955 | A | G | 1 | a0003c0009t0027g0307 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1076+3501T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148505955 | |||||||
chr5:148506002 | C | T | 4 | a0001c0004t0001g0242 a0001c0004t0003g0118 a0001c0006t0003g0110 others(1): Show |
4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1076+3454G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148506002 | |||||||
chr5:148506098 | G | A | 1 | a0001c0001t0020g0128 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1076+3358C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148506098 | |||||||
chr5:148506108 | A | C | 1 | a0001c0001t0003g0087 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1076+3348T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148506108 | |||||||
chr5:148506129 | C | T | 4 | a0001c0001t0002g0027 a0001c0001t0002g0052 a0001c0001t0003g0087 others(1): Show |
4 | HG00673.hp1 HG02074.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.1076+3327G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148506129 | |||||||
chr5:148506160 | T | G | 1 | a0001c0001t0001g0201 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1076+3296A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148506160 | |||||||
chr5:148506239 | T | A | 1 | a0001c0001t0002g0020 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1076+3217A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148506239 | |||||||
chr5:148506340 | G | T | 5 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0216 others(2): Show |
5 | HG01167.hp1 HG01884.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1076+3116C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148506340 | |||||||
chr5:148506360 | T | G | 4 | a0001c0001t0002g0027 a0001c0001t0002g0052 a0001c0001t0003g0087 others(1): Show |
4 | HG00673.hp1 HG02074.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.1076+3096A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148506360 | |||||||
chr5:148506419 | C | T | 6 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0190 others(3): Show |
7 | HG01074.hp1 HG01891.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1076+3037G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148506419 | |||||||
chr5:148506434 | G | A | 4 | a0001c0004t0001g0242 a0001c0004t0003g0118 a0001c0006t0003g0110 others(1): Show |
4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1076+3022C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148506434 | |||||||
chr5:148506442 | C | T | 1 | a0001c0001t0001g0203 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1076+3014G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148506442 | |||||||
chr5:148506448 | G | A | 164 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0177 others(161): Show |
166 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.1076+3008C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148506448 | |||||||
chr5:148506454 | T | G | 60 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(57): Show |
61 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.1076+3002A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148506454 | |||||||
chr5:148506486 | C | T | 1 | a0001c0001t0021g0106 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1076+2970G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148506486 | |||||||
chr5:148506496 | C | T | 1 | a0001c0001t0001g0294 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1076+2960G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148506496 | |||||||
chr5:148506545 | C | T | 3 | a0001c0001t0001g0163 a0001c0001t0001g0174 a0001c0001t0001g0180 |
3 | NA18994.hp1 NA19083.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.1076+2911G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148506545 | |||||||
chr5:148506594 | G | A | 164 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0177 others(161): Show |
166 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.1076+2862C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148506594 | |||||||
chr5:148506608 | T | G | 4 | a0001c0001t0001g0181 a0001c0001t0002g0035 a0001c0001t0002g0055 others(1): Show |
4 | HG02738.hp2 NA18951.hp1 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.1076+2848A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148506608 | |||||||
chr5:148506702 | A | G | 1 | a0001c0001t0001g0244 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1076+2754T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148506702 | |||||||
chr5:148506804 | C | G | 164 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0177 others(161): Show |
166 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.1076+2652G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148506804 | |||||||
chr5:148506994 | T | A | 4 | a0001c0004t0001g0242 a0001c0004t0003g0118 a0001c0006t0003g0110 others(1): Show |
4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1076+2462A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148506994 | |||||||
chr5:148507040 | C | T | 4 | a0001c0004t0001g0242 a0001c0004t0003g0118 a0001c0006t0003g0110 others(1): Show |
4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1076+2416G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148507040 | |||||||
chr5:148507113 | T | G | 1 | a0001c0001t0001g0225 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1076+2343A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148507113 | |||||||
chr5:148507138 | T | C | 22 | a0001c0001t0001g0202 a0001c0001t0001g0211 a0001c0001t0001g0213 others(19): Show |
22 | HG01243.hp2 HG01496.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.1076+2318A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148507138 | |||||||
chr5:148507202 | G | A | 91 | a0001c0001t0001g0185 a0001c0001t0001g0188 a0001c0001t0001g0193 others(88): Show |
91 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.1076+2254C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148507202 | |||||||
chr5:148507213 | C | T | 191 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0177 others(188): Show |
193 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.1076+2243G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148507213 | |||||||
chr5:148507267 | C | T | 1 | a0001c0006t0003g0110 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1076+2189G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148507267 | |||||||
chr5:148507384 | G | A | 4 | a0001c0004t0001g0242 a0001c0004t0003g0118 a0001c0006t0003g0110 others(1): Show |
4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1076+2072C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148507384 | |||||||
chr5:148507388 | G | C | 1 | a0001c0006t0003g0110 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1076+2068C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148507388 | |||||||
chr5:148507478 | G | C | 4 | a0001c0004t0001g0242 a0001c0004t0003g0118 a0001c0006t0003g0110 others(1): Show |
4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1076+1978C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148507478 | |||||||
chr5:148507488 | C | T | 4 | a0001c0001t0002g0027 a0001c0001t0002g0052 a0001c0001t0003g0087 others(1): Show |
4 | HG00673.hp1 HG02074.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.1076+1968G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148507488 | |||||||
chr5:148507489 | G | A | 5 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0190 others(2): Show |
6 | HG01891.hp1 HG02818.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1076+1967C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148507489 | |||||||
chr5:148507504 | C | T | 1 | a0001c0001t0010g0086 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1076+1952G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148507504 | |||||||
chr5:148507577 | CA | C | 178 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0164 others(175): Show |
180 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(177): Show |
intron_variant | MODIFIER | c.1076+1878delT | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148507577 | |||||||
chr5:148507907 | A | G | 1 | a0003c0009t0027g0307 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1076+1549T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148507907 | |||||||
chr5:148508025 | T | C | 1 | a0001c0001t0001g0204 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1076+1431A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148508025 | |||||||
chr5:148508122 | A | T | 1 | a0001c0001t0001g0216 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1076+1334T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148508122 | |||||||
chr5:148508186 | G | A | 4 | a0001c0004t0001g0242 a0001c0004t0003g0118 a0001c0006t0003g0110 others(1): Show |
4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1076+1270C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148508186 | |||||||
chr5:148508314 | T | C | 3 | a0001c0004t0001g0242 a0001c0004t0003g0118 a0003c0009t0027g0307 |
3 | HG01243.hp1 HG02300.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1076+1142A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148508314 | |||||||
chr5:148508409 | A | G | 3 | a0001c0001t0001g0183 a0001c0001t0001g0195 a0001c0001t0001g0196 |
3 | HG02486.hp1 HG02970.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1076+1047T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148508409 | |||||||
chr5:148508533 | A | G | 2 | a0001c0001t0007g0073 a0001c0001t0007g0074 |
2 | NA18957.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.1076+923T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148508533 | |||||||
chr5:148508536 | G | A | 1 | a0001c0001t0001g0291 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1076+920C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148508536 | |||||||
chr5:148508708 | A | G | 1 | a0001c0001t0006g0175 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1076+748T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148508708 | |||||||
chr5:148508710 | T | G | 4 | a0001c0004t0001g0242 a0001c0004t0003g0118 a0001c0006t0003g0110 others(1): Show |
4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1076+746A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148508710 | |||||||
chr5:148508801 | T | C | 1 | a0001c0001t0003g0100 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1076+655A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148508801 | |||||||
chr5:148508802 | A | G | 1 | a0001c0001t0026g0184 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1076+654T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148508802 | |||||||
chr5:148508921 | G | A | 4 | a0001c0004t0001g0242 a0001c0004t0003g0118 a0001c0006t0003g0110 others(1): Show |
4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1076+535C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148508921 | |||||||
chr5:148509032 | A | G | 1 | a0001c0001t0007g0048 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1076+424T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148509032 | |||||||
chr5:148509104 | C | T | 4 | a0001c0004t0001g0242 a0001c0004t0003g0118 a0001c0006t0003g0110 others(1): Show |
4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1076+352G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148509104 | |||||||
chr5:148509185 | T | A | 1 | a0001c0001t0003g0108 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1076+271A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148509185 | |||||||
chr5:148509202 | G | T | 1 | a0001c0001t0002g0068 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1076+254C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148509202 | |||||||
chr5:148509276 | TCCAGAGC others(12): Show |
T | 1 | a0001c0001t0002g0056 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1076+161_1076+179d others(21): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 6/6 | chr5 | 148509276 | |||||||
chr5:148510060 | A | G | 91 | a0001c0001t0001g0185 a0001c0001t0001g0188 a0001c0001t0001g0193 others(88): Show |
91 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.508-36T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148510060 | |||||||
chr5:148510114 | G | A | 4 | a0001c0004t0001g0242 a0001c0004t0003g0118 a0001c0006t0003g0110 others(1): Show |
4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-90C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148510114 | |||||||
chr5:148510139 | A | G | 37 | a0001c0001t0001g0161 a0001c0001t0001g0171 a0001c0001t0001g0183 others(34): Show |
37 | HG00738.hp2 HG01167.hp1 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.508-115T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148510139 | |||||||
chr5:148510180 | A | G | 99 | a0001c0001t0001g0185 a0001c0001t0001g0188 a0001c0001t0001g0193 others(96): Show |
99 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.508-156T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148510180 | |||||||
chr5:148510494 | A | G | 4 | a0001c0004t0001g0242 a0001c0004t0003g0118 a0001c0006t0003g0110 others(1): Show |
4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-470T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148510494 | |||||||
chr5:148510561 | C | T | 91 | a0001c0001t0001g0185 a0001c0001t0001g0188 a0001c0001t0001g0193 others(88): Show |
91 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.508-537G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148510561 | |||||||
chr5:148510693 | T | C | 4 | a0001c0004t0001g0242 a0001c0004t0003g0118 a0001c0006t0003g0110 others(1): Show |
4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-669A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148510693 | |||||||
chr5:148510697 | C | T | 4 | a0001c0004t0001g0242 a0001c0004t0003g0118 a0001c0006t0003g0110 others(1): Show |
4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-673G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148510697 | |||||||
chr5:148510722 | C | T | 4 | a0001c0004t0001g0242 a0001c0004t0003g0118 a0001c0006t0003g0110 others(1): Show |
4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-698G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148510722 | |||||||
chr5:148510727 | G | A | 1 | a0001c0001t0021g0106 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.508-703C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148510727 | |||||||
chr5:148510790 | ATAACACA others(3): Show |
A | 2 | a0001c0001t0004g0255 a0001c0001t0004g0256 |
2 | NA18943.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.508-776_508-767del others(10): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148510790 | |||||||
chr5:148510941 | T | C | 1 | a0001c0001t0002g0036 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.508-917A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148510941 | |||||||
chr5:148510982 | C | A | 5 | a0001c0001t0001g0260 a0001c0001t0006g0223 a0001c0001t0006g0229 others(2): Show |
5 | HG01257.hp1 HG01433.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.508-958G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148510982 | |||||||
chr5:148511173 | C | T | 4 | a0001c0004t0001g0242 a0001c0004t0003g0118 a0001c0006t0003g0110 others(1): Show |
4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-1149G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148511173 | |||||||
chr5:148511174 | G | A | 1 | a0001c0001t0001g0291 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.508-1150C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148511174 | |||||||
chr5:148511198 | G | A | 4 | a0001c0004t0001g0242 a0001c0004t0003g0118 a0001c0006t0003g0110 others(1): Show |
4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-1174C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148511198 | |||||||
chr5:148511347 | C | T | 1 | a0001c0001t0002g0009 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.508-1323G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148511347 | |||||||
chr5:148511437 | C | CTTTAA | 4 | a0001c0004t0001g0242 a0001c0004t0003g0118 a0001c0006t0003g0110 others(1): Show |
4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-1418_508-1414d others(7): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148511437 | |||||||
chr5:148511619 | T | G | 5 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0190 others(2): Show |
6 | HG01891.hp1 HG02818.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.508-1595A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148511619 | |||||||
chr5:148511619 | T | TGTGTGTG others(6): Show |
2 | a0001c0001t0002g0026 a0001c0001t0005g0139 |
2 | HG02698.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.508-1596_508-1595i others(15): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148511619 | |||||||
chr5:148511619 | T | TTG | 35 | a0001c0001t0001g0202 a0001c0001t0001g0211 a0001c0001t0001g0213 others(32): Show |
35 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(32): Show |
intron_variant | MODIFIER | c.508-1597_508-1596d others(4): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148511619 | |||||||
chr5:148511619 | T | TTGTG | 14 | a0001c0001t0001g0174 a0001c0001t0001g0180 a0001c0001t0001g0186 others(11): Show |
14 | HG01167.hp1 HG01884.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.508-1599_508-1596d others(6): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148511619 | |||||||
chr5:148511619 | T | TTGTGTG | 8 | a0001c0001t0001g0163 a0001c0001t0001g0251 a0001c0001t0001g0252 others(5): Show |
8 | HG02615.hp2 HG02622.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.508-1601_508-1596d others(8): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148511619 | |||||||
chr5:148511619 | T | TTGTGTGT others(1): Show |
3 | a0001c0001t0001g0188 a0001c0001t0001g0193 a0001c0001t0005g0142 |
3 | HG02976.hp2 HG03669.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.508-1603_508-1596d others(10): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148511619 | |||||||
chr5:148511619 | T | TTGTGTGT others(3): Show |
11 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0306 others(8): Show |
11 | HG01069.hp2 HG01071.hp2 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.508-1605_508-1596d others(12): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148511619 | |||||||
chr5:148511619 | T | TTGTGTGT others(5): Show |
25 | a0001c0001t0001g0185 a0001c0001t0001g0253 a0001c0001t0001g0303 others(22): Show |
25 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(22): Show |
intron_variant | MODIFIER | c.508-1607_508-1596d others(14): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148511619 | |||||||
chr5:148511619 | T | TTGTGTGT others(7): Show |
21 | a0001c0001t0001g0199 a0001c0001t0001g0232 a0001c0001t0001g0250 others(18): Show |
21 | HG00408.hp1 HG02056.hp1 HG02895.hp2 others(18): Show |
intron_variant | MODIFIER | c.508-1609_508-1596d others(16): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148511619 | |||||||
chr5:148511619 | T | TTGTGTGT others(9): Show |
4 | a0001c0001t0001g0245 a0001c0001t0002g0033 a0001c0001t0002g0063 others(1): Show |
4 | HG00621.hp2 HG03225.hp1 NA18947.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-1611_508-1596d others(18): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148511619 | |||||||
chr5:148511619 | TTG | T | 5 | a0001c0001t0001g0239 a0001c0001t0001g0260 a0001c0001t0002g0057 others(2): Show |
5 | HG02132.hp2 HG02735.hp2 NA18941.hp2 others(2): Show |
intron_variant | MODIFIER | c.508-1597_508-1596d others(4): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148511619 | |||||||
chr5:148511619 | TTGTG | T | 3 | a0001c0001t0001g0179 a0001c0001t0002g0021 a0001c0001t0003g0092 |
3 | HG02056.hp2 NA18522.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.508-1599_508-1596d others(6): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148511619 | |||||||
chr5:148511646 | T | C | 7 | a0001c0001t0001g0183 a0001c0001t0001g0195 a0001c0001t0001g0196 others(4): Show |
7 | HG02257.hp1 HG02451.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.508-1622A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148511646 | |||||||
chr5:148511647 | G | GTGTGTGT others(5): Show |
1 | a0001c0002t0003g0094 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.508-1635_508-1624d others(14): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148511647 | |||||||
chr5:148511701 | G | A | 1 | a0001c0006t0003g0110 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.508-1677C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148511701 | |||||||
chr5:148511846 | T | C | 1 | a0001c0001t0001g0182 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.508-1822A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148511846 | |||||||
chr5:148511851 | G | A | 22 | a0001c0001t0001g0202 a0001c0001t0001g0211 a0001c0001t0001g0213 others(19): Show |
22 | HG01243.hp2 HG01496.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.508-1827C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148511851 | |||||||
chr5:148511976 | G | T | 1 | a0001c0001t0001g0173 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.508-1952C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148511976 | |||||||
chr5:148512067 | C | T | 1 | a0001c0006t0003g0110 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.508-2043G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148512067 | |||||||
chr5:148512072 | G | A | 1 | a0001c0001t0005g0142 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.508-2048C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148512072 | |||||||
chr5:148512369 | T | C | 6 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0190 others(3): Show |
7 | HG01074.hp1 HG01891.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.508-2345A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148512369 | |||||||
chr5:148512411 | T | G | 1 | a0001c0001t0021g0106 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.508-2387A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148512411 | |||||||
chr5:148512441 | CTCTT | C | 4 | a0001c0001t0003g0102 a0001c0001t0006g0212 a0001c0001t0011g0103 others(1): Show |
4 | HG01496.hp2 HG02630.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.508-2421_508-2418d others(6): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148512441 | |||||||
chr5:148512581 | C | A | 1 | a0001c0001t0001g0304 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.508-2557G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148512581 | |||||||
chr5:148512619 | T | C | 1 | a0001c0001t0006g0200 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.508-2595A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148512619 | |||||||
chr5:148512657 | G | A | 1 | a0001c0006t0003g0110 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.508-2633C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148512657 | |||||||
chr5:148512661 | T | C | 1 | a0003c0009t0027g0307 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.508-2637A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148512661 | |||||||
chr5:148512718 | G | A | 1 | a0001c0001t0001g0269 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.508-2694C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148512718 | |||||||
chr5:148512826 | G | T | 1 | a0001c0001t0001g0238 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.508-2802C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148512826 | |||||||
chr5:148512967 | C | T | 4 | a0001c0004t0001g0242 a0001c0004t0003g0118 a0001c0006t0003g0110 others(1): Show |
4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-2943G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148512967 | |||||||
chr5:148513011 | T | C | 4 | a0001c0004t0001g0242 a0001c0004t0003g0118 a0001c0006t0003g0110 others(1): Show |
4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-2987A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148513011 | |||||||
chr5:148513040 | C | G | 1 | a0001c0001t0021g0106 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.508-3016G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148513040 | |||||||
chr5:148513065 | T | G | 9 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0216 others(6): Show |
9 | HG01167.hp1 HG01243.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.508-3041A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148513065 | |||||||
chr5:148513136 | G | A | 2 | a0001c0001t0001g0275 a0001c0001t0001g0289 |
2 | HG01516.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.508-3112C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148513136 | |||||||
chr5:148513415 | C | T | 1 | a0001c0001t0006g0212 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.508-3391G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148513415 | |||||||
chr5:148513469 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.508-3445C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148513469 | |||||||
chr5:148513685 | A | G | 1 | a0001c0001t0003g0102 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.508-3661T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148513685 | |||||||
chr5:148513712 | T | C | 4 | a0001c0004t0001g0242 a0001c0004t0003g0118 a0001c0006t0003g0110 others(1): Show |
4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-3688A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148513712 | |||||||
chr5:148513815 | C | G | 91 | a0001c0001t0001g0185 a0001c0001t0001g0188 a0001c0001t0001g0193 others(88): Show |
91 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.508-3791G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148513815 | |||||||
chr5:148513864 | C | T | 1 | a0001c0001t0002g0008 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.508-3840G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148513864 | |||||||
chr5:148513870 | C | T | 99 | a0001c0001t0001g0185 a0001c0001t0001g0188 a0001c0001t0001g0193 others(96): Show |
99 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.508-3846G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148513870 | |||||||
chr5:148514156 | A | G | 1 | a0001c0001t0001g0271 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.508-4132T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148514156 | |||||||
chr5:148514246 | T | C | 173 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0177 others(170): Show |
175 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.508-4222A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148514246 | |||||||
chr5:148514566 | A | G | 4 | a0001c0004t0001g0242 a0001c0004t0003g0118 a0001c0006t0003g0110 others(1): Show |
4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-4542T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148514566 | |||||||
chr5:148514596 | T | C | 1 | a0001c0001t0003g0099 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.508-4572A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148514596 | |||||||
chr5:148514679 | G | A | 22 | a0001c0001t0001g0202 a0001c0001t0001g0211 a0001c0001t0001g0213 others(19): Show |
22 | HG01243.hp2 HG01496.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.508-4655C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148514679 | |||||||
chr5:148514760 | A | C | 1 | a0001c0001t0002g0030 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.508-4736T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148514760 | |||||||
chr5:148514858 | A | T | 4 | a0001c0001t0002g0027 a0001c0001t0002g0052 a0001c0001t0003g0087 others(1): Show |
4 | HG00673.hp1 HG02074.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.508-4834T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148514858 | |||||||
chr5:148514931 | C | A | 3 | a0001c0001t0002g0020 a0001c0001t0002g0023 a0001c0001t0002g0024 |
3 | HG01928.hp2 HG01952.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.508-4907G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148514931 | |||||||
chr5:148515073 | A | G | 1 | a0001c0001t0001g0285 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.508-5049T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148515073 | |||||||
chr5:148515142 | G | A | 163 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0177 others(160): Show |
165 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.508-5118C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148515142 | |||||||
chr5:148515157 | C | T | 4 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0216 others(1): Show |
4 | HG01167.hp1 HG02622.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-5133G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148515157 | |||||||
chr5:148515316 | A | G | 4 | a0001c0004t0001g0242 a0001c0004t0003g0118 a0001c0006t0003g0110 others(1): Show |
4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-5292T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148515316 | |||||||
chr5:148515385 | C | T | 296 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0163 others(293): Show |
299 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(296): Show |
intron_variant | MODIFIER | c.508-5361G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148515385 | |||||||
chr5:148515389 | C | G | 4 | a0001c0004t0001g0242 a0001c0004t0003g0118 a0001c0006t0003g0110 others(1): Show |
4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-5365G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148515389 | |||||||
chr5:148515487 | T | G | 59 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(56): Show |
60 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.508-5463A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148515487 | |||||||
chr5:148515526 | A | T | 4 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0216 others(1): Show |
4 | HG01167.hp1 HG02622.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-5502T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148515526 | |||||||
chr5:148515556 | G | T | 95 | a0001c0001t0001g0185 a0001c0001t0001g0188 a0001c0001t0001g0193 others(92): Show |
95 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.508-5532C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148515556 | |||||||
chr5:148515575 | G | T | 163 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0177 others(160): Show |
165 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.508-5551C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148515575 | |||||||
chr5:148515690 | T | A | 1 | a0001c0001t0003g0092 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.508-5666A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148515690 | |||||||
chr5:148515720 | C | G | 1 | a0001c0006t0003g0110 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.508-5696G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148515720 | |||||||
chr5:148515754 | A | AT | 95 | a0001c0001t0001g0185 a0001c0001t0001g0188 a0001c0001t0001g0193 others(92): Show |
95 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.508-5731dupA | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148515754 | |||||||
chr5:148515791 | G | A | 1 | a0001c0001t0003g0101 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.508-5767C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148515791 | |||||||
chr5:148515818 | G | GT | 3 | a0001c0004t0001g0242 a0001c0004t0003g0118 a0003c0009t0027g0307 |
3 | HG01243.hp1 HG02300.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.508-5795dupA | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148515818 | |||||||
chr5:148515920 | CTGAA | C | 4 | a0001c0004t0001g0242 a0001c0004t0003g0118 a0001c0006t0003g0110 others(1): Show |
4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-5900_508-5897d others(6): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148515920 | |||||||
chr5:148515931 | T | G | 4 | a0001c0004t0001g0242 a0001c0004t0003g0118 a0001c0006t0003g0110 others(1): Show |
4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-5907A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148515931 | |||||||
chr5:148515985 | C | CAT | 59 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(56): Show |
60 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.508-5963_508-5962d others(4): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148515985 | |||||||
chr5:148516059 | A | T | 1 | a0001c0004t0001g0242 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.508-6035T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148516059 | |||||||
chr5:148516312 | C | CT | 29 | a0001c0001t0001g0161 a0001c0001t0001g0176 a0001c0001t0001g0181 others(26): Show |
30 | HG00741.hp1 HG02145.hp1 HG02572.hp1 others(27): Show |
intron_variant | MODIFIER | c.508-6289dupA | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148516312 | |||||||
chr5:148516312 | CT | C | 66 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0177 others(63): Show |
68 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.508-6289delA | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148516312 | |||||||
chr5:148516312 | CTT | C | 7 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0040 others(4): Show |
7 | HG00323.hp1 HG02738.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.508-6290_508-6289d others(4): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148516312 | |||||||
chr5:148516345 | G | A | 4 | a0001c0004t0001g0242 a0001c0004t0003g0118 a0001c0006t0003g0110 others(1): Show |
4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-6321C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148516345 | |||||||
chr5:148516376 | A | G | 1 | a0003c0009t0027g0307 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.508-6352T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148516376 | |||||||
chr5:148516389 | G | A | 1 | a0003c0009t0027g0307 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.508-6365C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148516389 | |||||||
chr5:148516422 | C | T | 1 | a0001c0001t0002g0045 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.508-6398G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148516422 | |||||||
chr5:148516465 | A | G | 4 | a0001c0004t0001g0242 a0001c0004t0003g0118 a0001c0006t0003g0110 others(1): Show |
4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-6441T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148516465 | |||||||
chr5:148516535 | G | T | 4 | a0001c0004t0001g0242 a0001c0004t0003g0118 a0001c0006t0003g0110 others(1): Show |
4 | HG01243.hp1 HG02300.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-6511C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148516535 | |||||||
chr5:148516564 | C | T | 1 | a0001c0001t0012g0220 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.508-6540G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148516564 | |||||||
chr5:148516597 | C | T | 4 | a0001c0001t0002g0027 a0001c0001t0002g0052 a0001c0001t0003g0087 others(1): Show |
4 | HG00673.hp1 HG02074.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.508-6573G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148516597 | |||||||
chr5:148516598 | G | A | 61 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(58): Show |
62 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.508-6574C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148516598 | |||||||
chr5:148516627 | C | CT | 10 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0216 others(7): Show |
10 | HG01167.hp1 HG01243.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.507+6565dupA | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148516627 | |||||||
chr5:148516627 | C | CTT | 7 | a0001c0001t0001g0183 a0001c0001t0001g0195 a0001c0001t0001g0196 others(4): Show |
7 | HG02257.hp1 HG02451.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.507+6564_507+6565d others(4): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148516627 | |||||||
chr5:148516627 | C | CTTTTT | 8 | a0001c0002t0001g0160 a0001c0002t0001g0162 a0001c0002t0001g0197 others(5): Show |
8 | HG02145.hp2 HG02451.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.507+6561_507+6565d others(7): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148516627 | |||||||
chr5:148516627 | C | CTTTTTT | 81 | a0001c0001t0001g0185 a0001c0001t0001g0188 a0001c0001t0001g0193 others(78): Show |
81 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.507+6560_507+6565d others(8): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148516627 | |||||||
chr5:148516664 | C | T | 4 | a0001c0001t0002g0027 a0001c0001t0002g0052 a0001c0001t0003g0087 others(1): Show |
4 | HG00673.hp1 HG02074.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.507+6529G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148516664 | |||||||
chr5:148516745 | G | A | 91 | a0001c0001t0001g0185 a0001c0001t0001g0188 a0001c0001t0001g0193 others(88): Show |
91 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.507+6448C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148516745 | |||||||
chr5:148516761 | T | C | 6 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0190 others(3): Show |
7 | HG01074.hp1 HG01891.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.507+6432A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148516761 | |||||||
chr5:148516971 | G | A | 62 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(59): Show |
63 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.507+6222C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148516971 | |||||||
chr5:148517280 | C | T | 1 | a0001c0002t0003g0094 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.507+5913G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148517280 | |||||||
chr5:148517391 | G | A | 11 | a0001c0001t0001g0192 a0001c0001t0001g0251 a0001c0001t0001g0252 others(8): Show |
11 | HG01516.hp2 HG01884.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.507+5802C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148517391 | |||||||
chr5:148517404 | A | G | 8 | a0001c0001t0001g0161 a0001c0001t0001g0171 a0001c0001t0001g0238 others(5): Show |
8 | HG00738.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.507+5789T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148517404 | |||||||
chr5:148517598 | G | A | 172 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0177 others(169): Show |
174 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.507+5595C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148517598 | |||||||
chr5:148517635 | CAAAAA | C | 167 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0177 others(164): Show |
169 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.507+5553_507+5557d others(7): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148517635 | |||||||
chr5:148517746 | G | A | 5 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0216 others(2): Show |
5 | HG01167.hp1 HG01884.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.507+5447C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148517746 | |||||||
chr5:148517767 | T | C | 1 | a0001c0001t0021g0106 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.507+5426A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148517767 | |||||||
chr5:148517874 | A | G | 95 | a0001c0001t0001g0185 a0001c0001t0001g0188 a0001c0001t0001g0193 others(92): Show |
95 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.507+5319T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148517874 | |||||||
chr5:148517916 | C | T | 1 | a0001c0001t0026g0184 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.507+5277G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148517916 | |||||||
chr5:148518349 | C | T | 5 | a0001c0001t0003g0102 a0001c0001t0006g0212 a0001c0001t0011g0103 others(2): Show |
5 | HG01496.hp2 HG02615.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.507+4844G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148518349 | |||||||
chr5:148518471 | G | C | 1 | a0001c0001t0001g0003 | 2 | HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.507+4722C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148518471 | |||||||
chr5:148518575 | C | A | 1 | a0001c0001t0003g0100 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.507+4618G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148518575 | |||||||
chr5:148518585 | A | C | 2 | a0001c0001t0001g0275 a0001c0001t0001g0289 |
2 | HG01516.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.507+4608T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148518585 | |||||||
chr5:148518608 | C | G | 1 | a0001c0001t0006g0175 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.507+4585G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148518608 | |||||||
chr5:148518637 | T | C | 1 | a0001c0001t0001g0182 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.507+4556A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148518637 | |||||||
chr5:148518828 | A | G | 1 | a0003c0009t0027g0307 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.507+4365T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148518828 | |||||||
chr5:148519076 | T | C | 1 | a0001c0001t0002g0008 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.507+4117A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148519076 | |||||||
chr5:148519126 | G | A | 62 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(59): Show |
63 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.507+4067C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148519126 | |||||||
chr5:148519262 | G | T | 95 | a0001c0001t0001g0185 a0001c0001t0001g0188 a0001c0001t0001g0193 others(92): Show |
95 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.507+3931C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148519262 | |||||||
chr5:148519327 | C | A | 8 | a0001c0002t0001g0160 a0001c0002t0001g0162 a0001c0002t0001g0197 others(5): Show |
8 | HG02145.hp2 HG02451.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.507+3866G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148519327 | |||||||
chr5:148519629 | T | G | 173 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0177 others(170): Show |
175 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.507+3564A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148519629 | |||||||
chr5:148519669 | T | C | 2 | a0001c0001t0001g0261 a0001c0001t0001g0262 |
2 | HG01192.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.507+3524A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148519669 | |||||||
chr5:148519785 | C | T | 1 | a0001c0001t0001g0244 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.507+3408G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148519785 | |||||||
chr5:148519826 | A | G | 1 | a0001c0001t0002g0076 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.507+3367T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148519826 | |||||||
chr5:148519882 | G | T | 1 | a0001c0001t0003g0117 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.507+3311C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148519882 | |||||||
chr5:148519962 | T | A | 9 | a0001c0001t0001g0164 a0001c0001t0004g0002 a0001c0001t0004g0165 others(6): Show |
10 | NA18947.hp2 NA18962.hp1 NA18963.hp1 others(7): Show |
intron_variant | MODIFIER | c.507+3231A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148519962 | |||||||
chr5:148519974 | A | G | 77 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0177 others(74): Show |
79 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.507+3219T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148519974 | |||||||
chr5:148520049 | T | C | 1 | a0001c0001t0001g0279 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.507+3144A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148520049 | |||||||
chr5:148520318 | G | A | 95 | a0001c0001t0001g0185 a0001c0001t0001g0188 a0001c0001t0001g0193 others(92): Show |
95 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.507+2875C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148520318 | |||||||
chr5:148520452 | C | T | 1 | a0001c0001t0001g0216 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.507+2741G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148520452 | |||||||
chr5:148521121 | G | A | 4 | a0001c0001t0001g0198 a0001c0001t0003g0114 a0001c0001t0003g0115 others(1): Show |
4 | HG02257.hp1 HG02451.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.507+2072C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148521121 | |||||||
chr5:148521376 | A | G | 5 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0216 others(2): Show |
5 | HG01167.hp1 HG01884.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.507+1817T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148521376 | |||||||
chr5:148521479 | T | C | 1 | a0001c0001t0001g0239 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.507+1714A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148521479 | |||||||
chr5:148521578 | TC | T | 60 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(57): Show |
61 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.507+1614delG | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148521578 | |||||||
chr5:148521630 | C | T | 95 | a0001c0001t0001g0185 a0001c0001t0001g0188 a0001c0001t0001g0193 others(92): Show |
95 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.507+1563G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148521630 | |||||||
chr5:148521938 | C | A | 2 | a0001c0001t0001g0292 a0001c0001t0005g0145 |
2 | HG00738.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.507+1255G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148521938 | |||||||
chr5:148522052 | G | A | 1 | a0001c0001t0002g0060 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.507+1141C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148522052 | |||||||
chr5:148522109 | G | A | 2 | a0001c0001t0002g0066 a0001c0001t0006g0257 |
2 | HG03239.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.507+1084C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148522109 | |||||||
chr5:148522206 | T | G | 1 | a0001c0001t0002g0037 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.507+987A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148522206 | |||||||
chr5:148522268 | A | T | 1 | a0001c0001t0002g0043 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.507+925T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148522268 | |||||||
chr5:148522269 | A | G | 1 | a0001c0001t0001g0269 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.507+924T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148522269 | |||||||
chr5:148522272 | A | T | 95 | a0001c0001t0001g0185 a0001c0001t0001g0188 a0001c0001t0001g0193 others(92): Show |
95 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.507+921T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148522272 | |||||||
chr5:148522323 | C | T | 92 | a0001c0001t0001g0185 a0001c0001t0001g0188 a0001c0001t0001g0193 others(89): Show |
92 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.507+870G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148522323 | |||||||
chr5:148522716 | C | G | 6 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0190 others(3): Show |
7 | HG01074.hp1 HG01891.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.507+477G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148522716 | |||||||
chr5:148522756 | T | C | 95 | a0001c0001t0001g0185 a0001c0001t0001g0188 a0001c0001t0001g0193 others(92): Show |
95 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.507+437A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148522756 | |||||||
chr5:148522765 | T | A | 1 | a0001c0001t0010g0086 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.507+428A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148522765 | |||||||
chr5:148522824 | C | T | 1 | a0001c0001t0001g0267 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.507+369G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148522824 | |||||||
chr5:148522982 | G | A | 1 | a0001c0001t0003g0126 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.507+211C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148522982 | |||||||
chr5:148523000 | G | C | 2 | a0001c0001t0001g0292 a0001c0001t0005g0145 |
2 | HG00738.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.507+193C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148523000 | |||||||
chr5:148523114 | C | A | 1 | a0001c0001t0003g0099 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.507+79G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148523114 | |||||||
chr5:148523140 | C | A | 95 | a0001c0001t0001g0185 a0001c0001t0001g0188 a0001c0001t0001g0193 others(92): Show |
95 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.507+53G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 5/6 | chr5 | 148523140 | |||||||
chr5:148523375 | G | C | 2 | a0001c0001t0001g0292 a0001c0001t0005g0145 |
2 | HG00738.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.354-29C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148523375 | |||||||
chr5:148523409 | G | A | 61 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(58): Show |
62 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.354-63C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148523409 | |||||||
chr5:148523516 | G | C | 1 | a0001c0001t0001g0237 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.354-170C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148523516 | |||||||
chr5:148523525 | G | T | 94 | a0001c0001t0001g0185 a0001c0001t0001g0188 a0001c0001t0001g0193 others(91): Show |
94 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.354-179C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148523525 | |||||||
chr5:148523553 | C | G | 1 | a0001c0001t0003g0108 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.354-207G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148523553 | |||||||
chr5:148523648 | A | C | 5 | a0001c0001t0001g0238 a0001c0001t0002g0046 a0001c0001t0002g0047 others(2): Show |
5 | HG02486.hp2 HG03017.hp2 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.354-302T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148523648 | |||||||
chr5:148523725 | C | T | 2 | a0001c0001t0001g0302 a0001c0001t0003g0117 |
2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.354-379G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148523725 | |||||||
chr5:148523769 | G | T | 2 | a0001c0001t0001g0292 a0001c0001t0005g0145 |
2 | HG00738.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.354-423C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148523769 | |||||||
chr5:148523844 | G | A | 1 | a0001c0001t0001g0261 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.354-498C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148523844 | |||||||
chr5:148523995 | G | GT | 92 | a0001c0001t0001g0185 a0001c0001t0001g0188 a0001c0001t0001g0193 others(89): Show |
92 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.354-650dupA | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148523995 | |||||||
chr5:148524089 | G | A | 4 | a0001c0001t0001g0192 a0001c0001t0008g0134 a0001c0001t0008g0135 others(1): Show |
4 | HG01884.hp2 HG03139.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.354-743C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148524089 | |||||||
chr5:148524089 | G | T | 6 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0231 others(3): Show |
6 | HG00597.hp1 HG02155.hp1 NA18612.hp2 others(3): Show |
intron_variant | MODIFIER | c.354-743C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148524089 | |||||||
chr5:148524181 | A | T | 1 | a0001c0001t0001g0291 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.354-835T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148524181 | |||||||
chr5:148524266 | T | G | 1 | a0001c0006t0003g0110 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.354-920A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148524266 | |||||||
chr5:148524333 | G | A | 3 | a0001c0001t0001g0281 a0001c0001t0001g0282 a0001c0001t0001g0283 |
3 | HG03239.hp2 HG03669.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.354-987C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148524333 | |||||||
chr5:148524678 | T | C | 91 | a0001c0001t0001g0185 a0001c0001t0001g0188 a0001c0001t0001g0193 others(88): Show |
91 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.354-1332A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148524678 | |||||||
chr5:148524683 | A | T | 5 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0216 others(2): Show |
5 | HG01167.hp1 HG01884.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.354-1337T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148524683 | |||||||
chr5:148524885 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.354-1539C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148524885 | |||||||
chr5:148524921 | G | T | 1 | a0001c0001t0002g0055 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.354-1575C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148524921 | |||||||
chr5:148524957 | C | T | 7 | a0001c0001t0001g0183 a0001c0001t0001g0195 a0001c0001t0001g0196 others(4): Show |
7 | HG02257.hp1 HG02451.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.354-1611G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148524957 | |||||||
chr5:148524990 | C | T | 4 | a0001c0001t0001g0224 a0001c0001t0001g0261 a0001c0001t0001g0262 others(1): Show |
4 | HG01192.hp1 HG01361.hp1 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.354-1644G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148524990 | |||||||
chr5:148525008 | T | G | 92 | a0001c0001t0001g0185 a0001c0001t0001g0188 a0001c0001t0001g0193 others(89): Show |
92 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.354-1662A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148525008 | |||||||
chr5:148525145 | A | T | 5 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0190 others(2): Show |
6 | HG01891.hp1 HG02818.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.354-1799T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148525145 | |||||||
chr5:148525237 | C | T | 1 | a0001c0001t0001g0230 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.354-1891G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148525237 | |||||||
chr5:148525456 | G | A | 1 | a0001c0001t0026g0184 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.354-2110C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148525456 | |||||||
chr5:148525518 | G | A | 60 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(57): Show |
61 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.354-2172C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148525518 | |||||||
chr5:148525768 | T | C | 4 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0216 others(1): Show |
4 | HG01167.hp1 HG02622.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.354-2422A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148525768 | |||||||
chr5:148525851 | G | C | 93 | a0001c0001t0001g0185 a0001c0001t0001g0188 a0001c0001t0001g0192 others(90): Show |
93 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.354-2505C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148525851 | |||||||
chr5:148525852 | G | A | 4 | a0001c0001t0001g0192 a0001c0004t0001g0242 a0001c0004t0003g0118 others(1): Show |
4 | HG01243.hp1 HG02300.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.354-2506C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148525852 | |||||||
chr5:148525992 | C | T | 1 | a0001c0001t0021g0106 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.354-2646G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148525992 | |||||||
chr5:148526000 | A | C | 1 | a0001c0001t0003g0115 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.354-2654T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148526000 | |||||||
chr5:148526006 | G | A | 1 | a0001c0001t0026g0184 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.354-2660C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148526006 | |||||||
chr5:148526116 | C | T | 6 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0190 others(3): Show |
7 | HG01074.hp1 HG01891.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.354-2770G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148526116 | |||||||
chr5:148526155 | G | A | 7 | a0001c0001t0001g0183 a0001c0001t0001g0195 a0001c0001t0001g0196 others(4): Show |
7 | HG02257.hp1 HG02451.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.354-2809C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148526155 | |||||||
chr5:148526442 | T | C | 89 | a0001c0001t0001g0185 a0001c0001t0001g0188 a0001c0001t0001g0193 others(86): Show |
89 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.354-3096A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148526442 | |||||||
chr5:148526766 | G | C | 3 | a0001c0001t0001g0252 a0001c0001t0010g0083 a0001c0001t0010g0084 |
3 | HG02615.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.354-3420C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148526766 | |||||||
chr5:148526940 | G | A | 3 | a0001c0001t0002g0063 a0001c0001t0002g0072 a0001c0001t0002g0076 |
3 | HG00621.hp2 HG02056.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.354-3594C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148526940 | |||||||
chr5:148526949 | T | A | 4 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0216 others(1): Show |
4 | HG01167.hp1 HG02622.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.354-3603A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148526949 | |||||||
chr5:148527140 | C | T | 61 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(58): Show |
62 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.354-3794G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148527140 | |||||||
chr5:148527338 | T | C | 1 | a0001c0001t0001g0243 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.354-3992A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148527338 | |||||||
chr5:148527435 | T | A | 89 | a0001c0001t0001g0185 a0001c0001t0001g0188 a0001c0001t0001g0193 others(86): Show |
89 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.354-4089A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148527435 | |||||||
chr5:148527686 | CT | C | 73 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0177 others(70): Show |
75 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.354-4341delA | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148527686 | |||||||
chr5:148527713 | C | T | 4 | a0001c0001t0002g0027 a0001c0001t0002g0052 a0001c0001t0003g0087 others(1): Show |
4 | HG00673.hp1 HG02074.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.354-4367G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148527713 | |||||||
chr5:148527726 | T | A | 1 | a0001c0001t0001g0171 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.354-4380A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148527726 | |||||||
chr5:148527826 | C | T | 1 | a0001c0004t0003g0118 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.354-4480G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148527826 | |||||||
chr5:148527930 | A | G | 1 | a0001c0005t0005g0146 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.354-4584T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148527930 | |||||||
chr5:148528016 | C | A | 2 | a0001c0001t0003g0111 a0001c0001t0004g0286 |
2 | HG00558.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.354-4670G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148528016 | |||||||
chr5:148528277 | G | T | 1 | a0001c0001t0021g0106 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.354-4931C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148528277 | |||||||
chr5:148528336 | A | T | 9 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0304 others(6): Show |
9 | HG01884.hp2 HG02615.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.354-4990T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148528336 | |||||||
chr5:148528337 | G | C | 4 | a0001c0001t0001g0192 a0001c0004t0001g0242 a0001c0004t0003g0118 others(1): Show |
4 | HG01243.hp1 HG02300.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.354-4991C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148528337 | |||||||
chr5:148528442 | C | T | 1 | a0001c0001t0002g0036 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.354-5096G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148528442 | |||||||
chr5:148528543 | GA | G | 73 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0177 others(70): Show |
75 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.354-5198delT | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148528543 | |||||||
chr5:148528770 | A | G | 1 | a0001c0001t0001g0244 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.354-5424T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148528770 | |||||||
chr5:148528782 | T | G | 61 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(58): Show |
62 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.354-5436A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148528782 | |||||||
chr5:148528822 | G | A | 73 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0177 others(70): Show |
75 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.354-5476C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148528822 | |||||||
chr5:148528825 | G | C | 1 | a0001c0001t0001g0260 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.354-5479C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148528825 | |||||||
chr5:148528853 | A | G | 1 | a0001c0001t0001g0269 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.354-5507T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148528853 | |||||||
chr5:148529084 | C | T | 4 | a0001c0001t0001g0192 a0001c0004t0001g0242 a0001c0004t0003g0118 others(1): Show |
4 | HG01243.hp1 HG02300.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.354-5738G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148529084 | |||||||
chr5:148529117 | C | T | 1 | a0001c0001t0001g0244 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.354-5771G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148529117 | |||||||
chr5:148529354 | C | A | 1 | a0001c0001t0011g0105 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.354-6008G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148529354 | |||||||
chr5:148529418 | G | C | 1 | a0001c0001t0012g0205 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.354-6072C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148529418 | |||||||
chr5:148529506 | C | T | 1 | a0001c0001t0011g0105 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.354-6160G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148529506 | |||||||
chr5:148529507 | G | A | 1 | a0001c0001t0001g0208 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.354-6161C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148529507 | |||||||
chr5:148529517 | A | T | 9 | a0001c0001t0002g0031 a0001c0001t0002g0033 a0001c0001t0002g0061 others(6): Show |
9 | HG00621.hp2 HG02056.hp1 NA18947.hp1 others(6): Show |
intron_variant | MODIFIER | c.354-6171T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148529517 | |||||||
chr5:148529525 | G | C | 1 | a0001c0001t0002g0019 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.354-6179C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148529525 | |||||||
chr5:148529556 | C | T | 1 | a0001c0001t0003g0112 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.354-6210G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148529556 | |||||||
chr5:148529647 | G | T | 1 | a0001c0001t0003g0087 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.354-6301C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148529647 | |||||||
chr5:148529889 | G | A | 4 | a0001c0001t0001g0192 a0001c0004t0001g0242 a0001c0004t0003g0118 others(1): Show |
4 | HG01243.hp1 HG02300.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.354-6543C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148529889 | |||||||
chr5:148530126 | A | T | 1 | a0001c0001t0003g0098 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.354-6780T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148530126 | |||||||
chr5:148530176 | G | A | 2 | a0001c0001t0003g0114 a0001c0001t0003g0115 |
2 | HG02886.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.354-6830C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148530176 | |||||||
chr5:148530325 | G | A | 88 | a0001c0001t0001g0185 a0001c0001t0001g0188 a0001c0001t0001g0193 others(85): Show |
88 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.354-6979C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148530325 | |||||||
chr5:148530382 | G | A | 1 | a0001c0001t0003g0087 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.354-7036C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148530382 | |||||||
chr5:148530534 | T | C | 1 | a0001c0001t0002g0056 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.354-7188A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148530534 | |||||||
chr5:148530576 | G | A | 5 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0216 others(2): Show |
5 | HG01167.hp1 HG01884.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.354-7230C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148530576 | |||||||
chr5:148530724 | C | A | 4 | a0001c0001t0001g0192 a0001c0004t0001g0242 a0001c0004t0003g0118 others(1): Show |
4 | HG01243.hp1 HG02300.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.354-7378G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148530724 | |||||||
chr5:148530727 | C | G | 1 | a0001c0001t0001g0282 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.354-7381G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148530727 | |||||||
chr5:148531070 | T | C | 1 | a0001c0001t0021g0106 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.354-7724A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148531070 | |||||||
chr5:148531297 | A | G | 99 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0185 others(96): Show |
100 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.354-7951T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148531297 | |||||||
chr5:148531307 | G | T | 1 | a0001c0001t0001g0269 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.354-7961C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148531307 | |||||||
chr5:148531510 | C | G | 16 | a0001c0001t0001g0183 a0001c0001t0001g0195 a0001c0001t0001g0196 others(13): Show |
16 | HG01884.hp2 HG02257.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.354-8164G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148531510 | |||||||
chr5:148531607 | A | G | 4 | a0001c0001t0003g0102 a0001c0001t0011g0103 a0001c0001t0011g0105 others(1): Show |
4 | HG01496.hp2 HG02615.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.354-8261T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148531607 | |||||||
chr5:148531611 | A | G | 1 | a0001c0001t0026g0184 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.354-8265T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148531611 | |||||||
chr5:148531915 | T | C | 1 | a0001c0006t0003g0110 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.354-8569A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148531915 | |||||||
chr5:148532060 | A | G | 170 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0177 others(167): Show |
172 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.354-8714T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148532060 | |||||||
chr5:148532120 | G | A | 1 | a0001c0001t0005g0139 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.354-8774C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148532120 | |||||||
chr5:148532153 | G | C | 6 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0190 others(3): Show |
7 | HG01074.hp1 HG01891.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.354-8807C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148532153 | |||||||
chr5:148532260 | C | T | 1 | a0001c0001t0010g0086 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.354-8914G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148532260 | |||||||
chr5:148532309 | G | A | 88 | a0001c0001t0001g0185 a0001c0001t0001g0188 a0001c0001t0001g0193 others(85): Show |
88 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.354-8963C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148532309 | |||||||
chr5:148532686 | C | T | 89 | a0001c0001t0001g0185 a0001c0001t0001g0188 a0001c0001t0001g0193 others(86): Show |
89 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.354-9340G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148532686 | |||||||
chr5:148532822 | C | T | 1 | a0003c0009t0027g0307 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.354-9476G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148532822 | |||||||
chr5:148532834 | C | A | 3 | a0001c0001t0003g0121 a0001c0001t0004g0293 a0001c0001t0004g0296 |
3 | NA18747.hp2 NA18965.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.354-9488G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148532834 | |||||||
chr5:148532993 | G | A | 9 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0304 others(6): Show |
9 | HG01884.hp2 HG02615.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.354-9647C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148532993 | |||||||
chr5:148533074 | C | T | 2 | a0001c0001t0008g0134 a0001c0001t0008g0135 |
2 | NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.354-9728G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148533074 | |||||||
chr5:148533292 | A | G | 4 | a0001c0001t0002g0027 a0001c0001t0002g0052 a0001c0001t0003g0087 others(1): Show |
4 | HG00673.hp1 HG02074.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.354-9946T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148533292 | |||||||
chr5:148533521 | T | C | 1 | a0001c0001t0001g0182 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.354-10175A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148533521 | |||||||
chr5:148533636 | G | A | 5 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0216 others(2): Show |
5 | HG01167.hp1 HG01884.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.354-10290C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148533636 | |||||||
chr5:148533650 | C | T | 1 | a0001c0001t0004g0158 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.354-10304G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148533650 | |||||||
chr5:148533734 | C | T | 4 | a0001c0001t0002g0027 a0001c0001t0002g0052 a0001c0001t0003g0087 others(1): Show |
4 | HG00673.hp1 HG02074.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.354-10388G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148533734 | |||||||
chr5:148533877 | ATAT | A | 3 | a0001c0001t0001g0192 a0001c0004t0001g0242 a0001c0004t0003g0118 |
3 | HG02300.hp2 HG03139.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.354-10534_354-1053 others(7): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148533877 | |||||||
chr5:148534098 | C | T | 94 | a0001c0001t0001g0185 a0001c0001t0001g0188 a0001c0001t0001g0192 others(91): Show |
94 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.354-10752G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148534098 | |||||||
chr5:148534177 | C | T | 1 | a0001c0001t0003g0129 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.354-10831G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148534177 | |||||||
chr5:148534633 | C | A | 1 | a0001c0001t0001g0282 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.354-11287G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148534633 | |||||||
chr5:148534664 | G | A | 1 | a0001c0001t0005g0145 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.354-11318C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148534664 | |||||||
chr5:148534717 | G | A | 1 | a0001c0001t0001g0243 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.354-11371C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148534717 | |||||||
chr5:148534852 | G | C | 1 | a0001c0001t0004g0158 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.354-11506C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148534852 | |||||||
chr5:148534926 | C | T | 1 | a0001c0001t0001g0182 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.354-11580G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148534926 | |||||||
chr5:148535084 | C | T | 1 | a0001c0001t0002g0058 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.354-11738G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148535084 | |||||||
chr5:148535101 | C | T | 89 | a0001c0001t0001g0185 a0001c0001t0001g0188 a0001c0001t0001g0193 others(86): Show |
89 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.354-11755G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148535101 | |||||||
chr5:148535324 | G | A | 3 | a0001c0001t0001g0161 a0001c0001t0001g0171 a0001c0001t0001g0301 |
3 | HG00738.hp2 HG02572.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.354-11978C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148535324 | |||||||
chr5:148535364 | G | A | 1 | a0001c0001t0003g0100 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.354-12018C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148535364 | |||||||
chr5:148535831 | G | A | 2 | a0001c0001t0001g0271 a0001c0001t0015g0014 |
2 | HG01981.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.354-12485C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148535831 | |||||||
chr5:148536082 | A | G | 1 | a0001c0006t0003g0110 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.353+12586T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148536082 | |||||||
chr5:148536097 | G | T | 10 | a0001c0001t0001g0164 a0001c0001t0001g0284 a0001c0001t0004g0002 others(7): Show |
11 | HG00558.hp1 NA18947.hp2 NA18962.hp1 others(8): Show |
intron_variant | MODIFIER | c.353+12571C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148536097 | |||||||
chr5:148536216 | T | C | 1 | a0001c0001t0001g0304 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.353+12452A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148536216 | |||||||
chr5:148536283 | C | T | 1 | a0001c0001t0006g0265 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.353+12385G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148536283 | |||||||
chr5:148536347 | C | A | 73 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0177 others(70): Show |
75 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.353+12321G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148536347 | |||||||
chr5:148536682 | G | A | 3 | a0001c0001t0001g0192 a0001c0004t0001g0242 a0001c0004t0003g0118 |
3 | HG02300.hp2 HG03139.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.353+11986C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148536682 | |||||||
chr5:148536722 | C | T | 1 | a0001c0001t0010g0086 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.353+11946G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148536722 | |||||||
chr5:148536744 | T | C | 4 | a0001c0001t0002g0027 a0001c0001t0002g0052 a0001c0001t0003g0087 others(1): Show |
4 | HG00673.hp1 HG02074.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.353+11924A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148536744 | |||||||
chr5:148536787 | G | C | 9 | a0001c0001t0001g0203 a0001c0001t0001g0248 a0001c0001t0001g0260 others(6): Show |
9 | HG01257.hp1 HG01433.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.353+11881C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148536787 | |||||||
chr5:148536835 | C | T | 1 | a0001c0001t0003g0100 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.353+11833G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148536835 | |||||||
chr5:148537049 | C | T | 4 | a0001c0001t0002g0027 a0001c0001t0002g0052 a0001c0001t0003g0087 others(1): Show |
4 | HG00673.hp1 HG02074.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.353+11619G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148537049 | |||||||
chr5:148537063 | C | T | 292 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0163 others(289): Show |
295 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(292): Show |
intron_variant | MODIFIER | c.353+11605G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148537063 | |||||||
chr5:148537204 | T | C | 1 | a0003c0009t0027g0307 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.353+11464A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148537204 | |||||||
chr5:148537215 | G | A | 3 | a0001c0001t0001g0192 a0001c0004t0001g0242 a0001c0004t0003g0118 |
3 | HG02300.hp2 HG03139.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.353+11453C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148537215 | |||||||
chr5:148537224 | A | G | 302 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0163 others(299): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.353+11444T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148537224 | |||||||
chr5:148537286 | T | A | 1 | a0001c0001t0002g0030 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.353+11382A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148537286 | |||||||
chr5:148537353 | C | T | 77 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0177 others(74): Show |
79 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.353+11315G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148537353 | |||||||
chr5:148537391 | A | T | 4 | a0001c0001t0002g0027 a0001c0001t0002g0052 a0001c0001t0003g0087 others(1): Show |
4 | HG00673.hp1 HG02074.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.353+11277T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148537391 | |||||||
chr5:148537953 | T | C | 1 | a0001c0001t0003g0122 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.353+10715A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148537953 | |||||||
chr5:148538106 | A | G | 3 | a0001c0001t0003g0120 a0001c0001t0003g0122 a0001c0001t0003g0129 |
3 | NA18981.hp2 NA18983.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.353+10562T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148538106 | |||||||
chr5:148538328 | C | T | 5 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0190 others(2): Show |
6 | HG01891.hp1 HG02818.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.353+10340G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148538328 | |||||||
chr5:148538354 | T | C | 1 | a0001c0001t0002g0010 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.353+10314A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148538354 | |||||||
chr5:148538477 | C | G | 1 | a0001c0001t0009g0153 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.353+10191G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148538477 | |||||||
chr5:148538486 | G | A | 1 | a0001c0001t0005g0141 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.353+10182C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148538486 | |||||||
chr5:148538584 | G | C | 68 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0177 others(65): Show |
70 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.353+10084C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148538584 | |||||||
chr5:148538631 | G | T | 1 | a0001c0001t0001g0234 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.353+10037C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148538631 | |||||||
chr5:148538915 | C | T | 2 | a0001c0001t0001g0264 a0001c0001t0005g0147 |
2 | HG02074.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.353+9753G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148538915 | |||||||
chr5:148538955 | C | T | 4 | a0001c0001t0001g0192 a0001c0004t0001g0242 a0001c0004t0003g0118 others(1): Show |
4 | HG01243.hp1 HG02300.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.353+9713G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148538955 | |||||||
chr5:148539010 | T | C | 1 | a0001c0001t0002g0047 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.353+9658A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148539010 | |||||||
chr5:148539211 | T | C | 89 | a0001c0001t0001g0185 a0001c0001t0001g0188 a0001c0001t0001g0193 others(86): Show |
89 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.353+9457A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148539211 | |||||||
chr5:148539270 | C | A | 7 | a0001c0001t0001g0183 a0001c0001t0001g0195 a0001c0001t0001g0196 others(4): Show |
7 | HG02257.hp1 HG02451.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.353+9398G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148539270 | |||||||
chr5:148539308 | G | A | 4 | a0001c0001t0001g0173 a0001c0001t0001g0190 a0001c0001t0001g0191 others(1): Show |
4 | HG01891.hp1 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.353+9360C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148539308 | |||||||
chr5:148539512 | C | A | 1 | a0001c0001t0001g0239 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.353+9156G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148539512 | |||||||
chr5:148539700 | T | A | 1 | a0001c0001t0007g0034 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.353+8968A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148539700 | |||||||
chr5:148539769 | G | A | 89 | a0001c0001t0001g0185 a0001c0001t0001g0188 a0001c0001t0001g0193 others(86): Show |
89 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.353+8899C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148539769 | |||||||
chr5:148539803 | A | G | 189 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0177 others(186): Show |
191 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.353+8865T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148539803 | |||||||
chr5:148539930 | T | C | 2 | a0001c0001t0001g0177 a0001c0001t0001g0178 |
2 | HG01361.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.353+8738A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148539930 | |||||||
chr5:148540147 | G | A | 1 | a0001c0001t0001g0216 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.353+8521C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148540147 | |||||||
chr5:148540200 | A | G | 1 | a0001c0001t0002g0077 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.353+8468T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148540200 | |||||||
chr5:148540211 | G | A | 1 | a0003c0009t0027g0307 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.353+8457C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148540211 | |||||||
chr5:148540309 | C | T | 8 | a0001c0001t0001g0183 a0001c0001t0001g0195 a0001c0001t0001g0196 others(5): Show |
8 | HG02486.hp1 HG02559.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.353+8359G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148540309 | |||||||
chr5:148540310 | G | A | 9 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0304 others(6): Show |
9 | HG01884.hp2 HG02615.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.353+8358C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148540310 | |||||||
chr5:148540400 | G | GTATA | 4 | a0001c0001t0001g0214 a0001c0001t0002g0028 a0001c0001t0004g0298 others(1): Show |
4 | HG00609.hp2 HG02559.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.353+8264_353+8267d others(6): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148540400 | |||||||
chr5:148540400 | G | GTATATA | 3 | a0001c0001t0002g0039 a0001c0001t0003g0098 a0001c0005t0005g0149 |
3 | HG00609.hp1 HG02735.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.353+8262_353+8267d others(8): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148540400 | |||||||
chr5:148540400 | G | GTATATAT others(3): Show |
1 | a0001c0001t0001g0295 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.353+8258_353+8267d others(12): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148540400 | |||||||
chr5:148540400 | GTA | G | 70 | a0001c0001t0001g0003 a0001c0001t0001g0163 a0001c0001t0001g0164 others(67): Show |
72 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.353+8266_353+8267d others(4): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148540400 | |||||||
chr5:148540400 | GTATA | G | 47 | a0001c0001t0001g0161 a0001c0001t0001g0181 a0001c0001t0001g0187 others(44): Show |
47 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.353+8264_353+8267d others(6): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148540400 | |||||||
chr5:148540400 | GTATATA | G | 57 | a0001c0001t0001g0176 a0001c0001t0001g0186 a0001c0001t0001g0199 others(54): Show |
57 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.353+8262_353+8267d others(8): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148540400 | |||||||
chr5:148540400 | GTATATAT others(1): Show |
G | 23 | a0001c0001t0001g0171 a0001c0001t0001g0177 a0001c0001t0001g0178 others(20): Show |
23 | HG00140.hp1 HG00423.hp1 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.353+8260_353+8267d others(10): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148540400 | |||||||
chr5:148540400 | GTATATAT others(3): Show |
G | 15 | a0001c0001t0001g0249 a0001c0001t0001g0264 a0001c0001t0002g0009 others(12): Show |
15 | HG00408.hp2 HG00438.hp2 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.353+8258_353+8267d others(12): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148540400 | |||||||
chr5:148540400 | GTATATAT others(5): Show |
G | 28 | a0001c0001t0001g0179 a0001c0001t0001g0201 a0001c0001t0001g0204 others(25): Show |
29 | HG00099.hp2 HG00323.hp1 HG00597.hp2 others(26): Show |
intron_variant | MODIFIER | c.353+8256_353+8267d others(14): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148540400 | |||||||
chr5:148540400 | GTATATAT others(7): Show |
G | 2 | a0001c0001t0002g0077 a0001c0006t0003g0110 |
2 | HG01516.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.353+8254_353+8267d others(16): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148540400 | |||||||
chr5:148540400 | GTATATAT others(13): Show |
G | 1 | a0001c0001t0002g0021 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.353+8248_353+8267d others(22): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148540400 | |||||||
chr5:148540400 | GTATATAT others(15): Show |
G | 1 | a0001c0001t0001g0221 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.353+8246_353+8267d others(24): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148540400 | |||||||
chr5:148540400 | GTATATAT others(25): Show |
G | 2 | a0001c0001t0001g0281 a0003c0009t0027g0307 |
2 | HG01243.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.353+8236_353+8267d others(34): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148540400 | |||||||
chr5:148540402 | A | G | 3 | a0001c0001t0003g0087 a0001c0001t0003g0100 a0001c0004t0001g0242 |
3 | HG00673.hp1 HG02300.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.353+8266T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148540402 | |||||||
chr5:148540404 | A | G | 6 | a0001c0001t0001g0192 a0001c0001t0002g0027 a0001c0001t0002g0052 others(3): Show |
6 | HG02074.hp1 HG02135.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.353+8264T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148540404 | |||||||
chr5:148540406 | A | G | 3 | a0001c0001t0001g0198 a0001c0001t0002g0044 a0001c0001t0005g0145 |
3 | HG01978.hp2 HG02257.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.353+8262T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148540406 | |||||||
chr5:148540408 | A | G | 6 | a0001c0001t0001g0279 a0001c0001t0001g0292 a0001c0001t0003g0093 others(3): Show |
6 | HG00738.hp1 HG02258.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.353+8260T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148540408 | |||||||
chr5:148540410 | A | G | 14 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0209 others(11): Show |
14 | HG00140.hp1 HG00423.hp1 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.353+8258T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148540410 | |||||||
chr5:148540412 | A | G | 13 | a0001c0001t0001g0249 a0001c0001t0001g0264 a0001c0001t0002g0009 others(10): Show |
13 | HG00408.hp2 HG00438.hp2 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.353+8256T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148540412 | |||||||
chr5:148540414 | A | G | 25 | a0001c0001t0001g0179 a0001c0001t0001g0201 a0001c0001t0001g0204 others(22): Show |
26 | HG00099.hp2 HG00323.hp1 HG00597.hp2 others(23): Show |
intron_variant | MODIFIER | c.353+8254T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148540414 | |||||||
chr5:148540416 | A | G | 2 | a0001c0001t0002g0077 a0001c0006t0003g0110 |
2 | HG01516.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.353+8252T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148540416 | |||||||
chr5:148540531 | A | G | 77 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0177 others(74): Show |
79 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.353+8137T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148540531 | |||||||
chr5:148540829 | C | G | 1 | a0001c0001t0001g0269 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.353+7839G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148540829 | |||||||
chr5:148540919 | C | T | 1 | a0001c0001t0001g0248 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.353+7749G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148540919 | |||||||
chr5:148541074 | C | T | 1 | a0001c0001t0002g0010 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.353+7594G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148541074 | |||||||
chr5:148541323 | A | T | 94 | a0001c0001t0001g0185 a0001c0001t0001g0188 a0001c0001t0001g0192 others(91): Show |
94 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.353+7345T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148541323 | |||||||
chr5:148541378 | C | T | 4 | a0001c0001t0002g0027 a0001c0001t0002g0052 a0001c0001t0003g0087 others(1): Show |
4 | HG00673.hp1 HG02074.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.353+7290G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148541378 | |||||||
chr5:148541635 | G | A | 1 | a0001c0001t0001g0237 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.353+7033C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148541635 | |||||||
chr5:148541741 | G | A | 1 | a0001c0001t0003g0100 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.353+6927C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148541741 | |||||||
chr5:148541962 | T | A | 59 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(56): Show |
60 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.353+6706A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148541962 | |||||||
chr5:148542433 | G | A | 1 | a0001c0001t0002g0017 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.353+6235C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148542433 | |||||||
chr5:148542489 | G | A | 4 | a0001c0001t0001g0209 a0001c0001t0001g0285 a0001c0001t0002g0078 others(1): Show |
4 | NA18945.hp1 NA18949.hp2 NA18952.hp2 others(1): Show |
intron_variant | MODIFIER | c.353+6179C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148542489 | |||||||
chr5:148542499 | A | T | 68 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0177 others(65): Show |
70 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.353+6169T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148542499 | |||||||
chr5:148542520 | G | A | 1 | a0001c0001t0002g0024 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.353+6148C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148542520 | |||||||
chr5:148542587 | A | C | 1 | a0001c0001t0001g0243 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.353+6081T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148542587 | |||||||
chr5:148542617 | T | G | 5 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0190 others(2): Show |
6 | HG01891.hp1 HG02818.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.353+6051A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148542617 | |||||||
chr5:148542725 | A | G | 1 | a0001c0001t0001g0236 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.353+5943T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148542725 | |||||||
chr5:148542790 | A | G | 90 | a0001c0001t0001g0185 a0001c0001t0001g0188 a0001c0001t0001g0193 others(87): Show |
90 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.353+5878T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148542790 | |||||||
chr5:148542870 | C | G | 1 | a0001c0001t0001g0269 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.353+5798G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148542870 | |||||||
chr5:148543317 | A | G | 1 | a0001c0001t0001g0244 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.353+5351T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148543317 | |||||||
chr5:148543418 | C | T | 1 | a0001c0001t0003g0095 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.353+5250G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148543418 | |||||||
chr5:148543551 | A | G | 189 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0177 others(186): Show |
191 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.353+5117T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148543551 | |||||||
chr5:148543814 | A | G | 172 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0177 others(169): Show |
174 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.353+4854T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148543814 | |||||||
chr5:148544084 | T | TAAAATGT others(313): Show |
2 | a0001c0001t0004g0297 a0001c0001t0014g0004 |
2 | HG00438.hp1 HG00544.hp1 |
intron_variant | MODIFIER | c.353+4583_353+4584i others(322): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148544084 | |||||||
chr5:148544084 | T | TAAAATGT others(314): Show |
1 | a0001c0001t0003g0099 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.353+4583_353+4584i others(323): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148544084 | |||||||
chr5:148544084 | T | TAAAATGT others(317): Show |
1 | a0001c0001t0003g0108 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.353+4583_353+4584i others(326): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148544084 | |||||||
chr5:148544084 | T | TAAAATGT others(318): Show |
1 | a0001c0001t0003g0113 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.353+4583_353+4584i others(327): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148544084 | |||||||
chr5:148544084 | T | TAAAATGT others(326): Show |
1 | a0001c0001t0004g0298 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.353+4583_353+4584i others(335): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148544084 | |||||||
chr5:148544084 | T | TAAAATGT others(327): Show |
4 | a0001c0001t0001g0254 a0001c0001t0001g0277 a0001c0001t0004g0255 others(1): Show |
4 | NA18943.hp1 NA18945.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.353+4583_353+4584i others(336): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148544084 | |||||||
chr5:148544084 | T | TAAAATGT others(328): Show |
1 | a0001c0001t0001g0266 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.353+4583_353+4584i others(337): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148544084 | |||||||
chr5:148544084 | T | TAAAATGT others(329): Show |
1 | a0001c0001t0001g0295 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.353+4583_353+4584i others(338): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148544084 | |||||||
chr5:148544084 | T | TAAAATGT others(330): Show |
1 | a0001c0001t0004g0293 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.353+4583_353+4584i others(339): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148544084 | |||||||
chr5:148544084 | T | TAAAATGT others(331): Show |
3 | a0001c0001t0003g0121 a0001c0001t0004g0170 a0001c0001t0004g0296 |
3 | NA18747.hp2 NA18962.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.353+4583_353+4584i others(340): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148544084 | |||||||
chr5:148544084 | T | TAAAATGT others(332): Show |
4 | a0001c0001t0001g0164 a0001c0001t0001g0284 a0001c0001t0001g0294 others(1): Show |
4 | HG00558.hp1 NA18957.hp2 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.353+4583_353+4584i others(341): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148544084 | |||||||
chr5:148544084 | T | TAAAATGT others(333): Show |
3 | a0001c0001t0004g0002 a0001c0001t0004g0165 a0001c0001t0004g0166 |
4 | NA18964.hp1 NA18991.hp1 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.353+4583_353+4584i others(342): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148544084 | |||||||
chr5:148544084 | T | TAAAATGT others(334): Show |
2 | a0001c0001t0004g0167 a0001c0001t0004g0169 |
2 | NA18947.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.353+4583_353+4584i others(343): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148544084 | |||||||
chr5:148544084 | T | TAAAATGT others(337): Show |
1 | a0001c0001t0020g0128 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.353+4583_353+4584i others(346): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148544084 | |||||||
chr5:148544084 | T | TAAAATGT others(351): Show |
1 | a0001c0001t0001g0228 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.353+4583_353+4584i others(360): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148544084 | |||||||
chr5:148544201 | C | T | 3 | a0001c0001t0001g0281 a0001c0001t0001g0282 a0001c0001t0001g0283 |
3 | HG03239.hp2 HG03669.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.353+4467G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148544201 | |||||||
chr5:148544278 | TCTCTCTT others(15): Show |
T | 190 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0177 others(187): Show |
192 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.353+4368_353+4389d others(24): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148544278 | |||||||
chr5:148544343 | A | C | 61 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(58): Show |
62 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.353+4325T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148544343 | |||||||
chr5:148544349 | A | C | 61 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(58): Show |
62 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.353+4319T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148544349 | |||||||
chr5:148544379 | A | G | 4 | a0001c0001t0002g0027 a0001c0001t0002g0052 a0001c0001t0003g0087 others(1): Show |
4 | HG00673.hp1 HG02074.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.353+4289T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148544379 | |||||||
chr5:148544483 | G | T | 1 | a0001c0001t0002g0063 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.353+4185C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148544483 | |||||||
chr5:148544489 | A | T | 1 | a0001c0001t0001g0192 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.353+4179T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148544489 | |||||||
chr5:148544692 | T | A | 2 | a0001c0001t0001g0280 a0001c0001t0025g0270 |
2 | HG00099.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.353+3976A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148544692 | |||||||
chr5:148544849 | C | T | 1 | a0003c0009t0027g0307 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.353+3819G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148544849 | |||||||
chr5:148544947 | G | A | 90 | a0001c0001t0001g0185 a0001c0001t0001g0188 a0001c0001t0001g0193 others(87): Show |
90 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.353+3721C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148544947 | |||||||
chr5:148545422 | A | T | 171 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0177 others(168): Show |
173 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.353+3246T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148545422 | |||||||
chr5:148545436 | C | T | 1 | a0001c0001t0002g0044 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.353+3232G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148545436 | |||||||
chr5:148545573 | A | C | 4 | a0001c0001t0001g0192 a0001c0004t0001g0242 a0001c0004t0003g0118 others(1): Show |
4 | HG01243.hp1 HG02300.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.353+3095T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148545573 | |||||||
chr5:148545628 | G | A | 1 | a0001c0001t0003g0127 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.353+3040C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148545628 | |||||||
chr5:148545688 | G | C | 4 | a0001c0001t0001g0192 a0001c0004t0001g0242 a0001c0004t0003g0118 others(1): Show |
4 | HG01243.hp1 HG02300.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.353+2980C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148545688 | |||||||
chr5:148545700 | T | C | 1 | a0001c0001t0001g0187 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.353+2968A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148545700 | |||||||
chr5:148545735 | G | T | 1 | a0001c0001t0001g0288 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.353+2933C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148545735 | |||||||
chr5:148545750 | G | T | 1 | a0001c0006t0003g0110 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.353+2918C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148545750 | |||||||
chr5:148545828 | A | G | 5 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0216 others(2): Show |
5 | HG01167.hp1 HG01884.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.353+2840T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148545828 | |||||||
chr5:148545899 | T | C | 1 | a0001c0001t0016g0067 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.353+2769A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148545899 | |||||||
chr5:148545942 | T | C | 1 | a0001c0001t0012g0205 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.353+2726A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148545942 | |||||||
chr5:148546000 | G | C | 61 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(58): Show |
62 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.353+2668C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148546000 | |||||||
chr5:148546236 | A | G | 2 | a0001c0001t0001g0302 a0001c0001t0003g0117 |
2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.353+2432T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148546236 | |||||||
chr5:148546258 | G | A | 2 | a0001c0001t0002g0007 a0001c0001t0007g0006 |
2 | HG00423.hp2 HG00544.hp2 |
intron_variant | MODIFIER | c.353+2410C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148546258 | |||||||
chr5:148546491 | A | G | 2 | a0001c0005t0005g0146 a0001c0005t0005g0149 |
2 | HG02559.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.353+2177T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148546491 | |||||||
chr5:148546589 | C | T | 4 | a0001c0001t0002g0027 a0001c0001t0002g0052 a0001c0001t0003g0087 others(1): Show |
4 | HG00673.hp1 HG02074.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.353+2079G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148546589 | |||||||
chr5:148546638 | T | A | 7 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0190 others(4): Show |
8 | HG01074.hp1 HG01891.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.353+2030A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148546638 | |||||||
chr5:148546674 | C | T | 68 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0177 others(65): Show |
70 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.353+1994G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148546674 | |||||||
chr5:148547112 | T | G | 3 | a0001c0001t0003g0120 a0001c0001t0003g0122 a0001c0001t0003g0129 |
3 | NA18981.hp2 NA18983.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.353+1556A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148547112 | |||||||
chr5:148547347 | G | A | 1 | a0001c0001t0001g0291 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.353+1321C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148547347 | |||||||
chr5:148547388 | G | A | 97 | a0001c0001t0001g0185 a0001c0001t0001g0188 a0001c0001t0001g0192 others(94): Show |
97 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.353+1280C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148547388 | |||||||
chr5:148547436 | G | T | 3 | a0001c0001t0001g0183 a0001c0001t0001g0195 a0001c0001t0001g0196 |
3 | HG02486.hp1 HG02970.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.353+1232C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148547436 | |||||||
chr5:148547526 | A | AAAAAT | 98 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0164 others(95): Show |
99 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.353+1137_353+1141d others(7): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148547526 | |||||||
chr5:148547526 | A | AAAAATAA others(3): Show |
13 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0203 others(10): Show |
13 | HG00140.hp1 HG01257.hp1 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.353+1132_353+1141d others(12): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148547526 | |||||||
chr5:148547526 | A | AAAAATAA others(8): Show |
1 | a0001c0001t0003g0101 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.353+1127_353+1141d others(17): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148547526 | |||||||
chr5:148547526 | A | AAAAATAA others(13): Show |
2 | a0001c0001t0003g0100 a0001c0001t0021g0106 |
2 | HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.353+1122_353+1141d others(22): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148547526 | |||||||
chr5:148547526 | A | AAAAATAA others(28): Show |
1 | a0001c0006t0003g0110 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.353+1107_353+1141d others(37): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148547526 | |||||||
chr5:148547526 | AAAAAT | A | 12 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0251 others(9): Show |
12 | HG01884.hp1 HG01884.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.353+1137_353+1141d others(7): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148547526 | |||||||
chr5:148547562 | A | AAAAT | 90 | a0001c0001t0001g0185 a0001c0001t0001g0188 a0001c0001t0001g0193 others(87): Show |
90 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.353+1102_353+1105d others(6): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148547562 | |||||||
chr5:148547562 | A | AAAATAAA others(2): Show |
27 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0186 others(24): Show |
28 | HG00673.hp1 HG00741.hp2 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.353+1105_353+1106i others(11): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148547562 | |||||||
chr5:148547562 | A | AAAATAAA others(7): Show |
37 | a0001c0001t0001g0179 a0001c0001t0001g0201 a0001c0001t0001g0204 others(34): Show |
38 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(35): Show |
intron_variant | MODIFIER | c.353+1105_353+1106i others(16): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148547562 | |||||||
chr5:148547562 | A | AAAATAAA others(12): Show |
8 | a0001c0001t0001g0285 a0001c0001t0002g0009 a0001c0001t0002g0018 others(5): Show |
8 | HG02300.hp2 HG02738.hp1 NA18747.hp1 others(5): Show |
intron_variant | MODIFIER | c.353+1105_353+1106i others(21): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148547562 | |||||||
chr5:148547562 | A | AAAATAAA others(17): Show |
2 | a0001c0001t0001g0192 a0001c0001t0001g0244 |
2 | HG03139.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.353+1105_353+1106i others(26): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148547562 | |||||||
chr5:148547562 | A | AAAATAAA others(6): Show |
1 | a0001c0001t0006g0268 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.353+1105_353+1106i others(15): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148547562 | |||||||
chr5:148547566 | T | TAAAATAA others(14): Show |
1 | a0001c0001t0001g0209 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.353+1101_353+1102i others(23): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148547566 | |||||||
chr5:148547570 | T | A | 1 | a0001c0001t0001g0228 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.353+1098A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148547570 | |||||||
chr5:148547668 | G | A | 4 | a0001c0001t0002g0027 a0001c0001t0002g0052 a0001c0001t0003g0087 others(1): Show |
4 | HG00673.hp1 HG02074.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.353+1000C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148547668 | |||||||
chr5:148547688 | C | T | 97 | a0001c0001t0001g0185 a0001c0001t0001g0188 a0001c0001t0001g0192 others(94): Show |
97 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.353+980G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148547688 | |||||||
chr5:148547748 | A | C | 1 | a0001c0006t0003g0110 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.353+920T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148547748 | |||||||
chr5:148547791 | G | A | 1 | a0001c0001t0001g0192 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.353+877C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148547791 | |||||||
chr5:148547816 | C | G | 1 | a0001c0001t0001g0253 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.353+852G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148547816 | |||||||
chr5:148547978 | A | G | 1 | a0001c0001t0002g0054 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.353+690T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148547978 | |||||||
chr5:148548028 | A | T | 1 | a0001c0001t0001g0192 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.353+640T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148548028 | |||||||
chr5:148548094 | G | T | 61 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(58): Show |
62 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.353+574C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148548094 | |||||||
chr5:148548166 | A | G | 1 | a0001c0001t0003g0112 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.353+502T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148548166 | |||||||
chr5:148548336 | T | C | 97 | a0001c0001t0001g0185 a0001c0001t0001g0188 a0001c0001t0001g0192 others(94): Show |
97 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.353+332A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148548336 | |||||||
chr5:148548555 | A | G | 2 | a0001c0001t0002g0061 a0001c0001t0007g0065 |
2 | NA19075.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.353+113T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148548555 | |||||||
chr5:148548567 | T | C | 59 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(56): Show |
60 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.353+101A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148548567 | |||||||
chr5:148548662 | C | T | 96 | a0001c0001t0001g0185 a0001c0001t0001g0188 a0001c0001t0001g0192 others(93): Show |
96 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(93): Show |
splice_region_variant&intron_variant | LOW | c.353+6G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 4/6 | chr5 | 148548662 | |||||||
chr5:148549025 | T | C | 4 | a0001c0001t0002g0027 a0001c0001t0002g0052 a0001c0001t0003g0087 others(1): Show |
4 | HG00673.hp1 HG02074.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.153-157A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 3/6 | chr5 | 148549025 | |||||||
chr5:148549094 | G | A | 4 | a0001c0001t0002g0027 a0001c0001t0002g0052 a0001c0001t0003g0087 others(1): Show |
4 | HG00673.hp1 HG02074.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.153-226C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 3/6 | chr5 | 148549094 | |||||||
chr5:148549118 | C | T | 60 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(57): Show |
61 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.153-250G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 3/6 | chr5 | 148549118 | |||||||
chr5:148549198 | C | T | 1 | a0003c0009t0027g0307 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.153-330G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 3/6 | chr5 | 148549198 | |||||||
chr5:148549759 | G | C | 1 | a0001c0001t0004g0170 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.152+378C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 3/6 | chr5 | 148549759 | |||||||
chr5:148549771 | CA | C | 41 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(38): Show |
42 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(39): Show |
intron_variant | MODIFIER | c.152+365delT | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 3/6 | chr5 | 148549771 | |||||||
chr5:148549812 | C | A | 2 | a0001c0001t0002g0057 a0001c0001t0002g0058 |
2 | NA18941.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.152+325G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 3/6 | chr5 | 148549812 | |||||||
chr5:148549987 | C | T | 6 | a0001c0001t0001g0185 a0001c0001t0001g0188 a0001c0001t0001g0246 others(3): Show |
6 | HG01069.hp2 HG01071.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.152+150G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 3/6 | chr5 | 148549987 | |||||||
chr5:148550117 | G | A | 1 | a0001c0001t0021g0106 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.152+20C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 3/6 | chr5 | 148550117 | |||||||
chr5:148550393 | G | A | 1 | a0001c0001t0004g0158 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.27-131C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148550393 | |||||||
chr5:148550435 | A | G | 4 | a0001c0001t0003g0102 a0001c0001t0011g0103 a0001c0001t0011g0105 others(1): Show |
4 | HG01496.hp2 HG02615.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.27-173T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148550435 | |||||||
chr5:148550967 | C | G | 1 | a0001c0001t0001g0203 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.27-705G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148550967 | |||||||
chr5:148551013 | G | A | 4 | a0001c0001t0002g0027 a0001c0001t0002g0052 a0001c0001t0003g0087 others(1): Show |
4 | HG00673.hp1 HG02074.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.27-751C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148551013 | |||||||
chr5:148551032 | CT | C | 6 | a0001c0001t0002g0025 a0001c0001t0002g0057 a0001c0001t0002g0058 others(3): Show |
6 | HG01952.hp1 HG02148.hp2 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.27-771delA | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148551032 | |||||||
chr5:148551194 | G | A | 2 | a0001c0001t0001g0266 a0001c0001t0001g0277 |
2 | NA19011.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.27-932C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148551194 | |||||||
chr5:148551259 | G | T | 1 | a0001c0001t0003g0121 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.27-997C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148551259 | |||||||
chr5:148551558 | T | C | 1 | a0001c0001t0001g0171 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.27-1296A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148551558 | |||||||
chr5:148551802 | G | C | 3 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0287 |
3 | HG01167.hp1 HG02622.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.27-1540C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148551802 | |||||||
chr5:148551960 | G | A | 91 | a0001c0001t0001g0185 a0001c0001t0001g0188 a0001c0001t0001g0193 others(88): Show |
91 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.27-1698C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148551960 | |||||||
chr5:148552094 | G | A | 1 | a0001c0001t0005g0144 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.27-1832C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148552094 | |||||||
chr5:148552134 | C | T | 61 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(58): Show |
62 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.27-1872G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148552134 | |||||||
chr5:148552180 | A | G | 4 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0216 others(1): Show |
4 | HG01167.hp1 HG02622.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.27-1918T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148552180 | |||||||
chr5:148552389 | A | T | 1 | a0001c0001t0004g0167 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.27-2127T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148552389 | |||||||
chr5:148552411 | C | T | 5 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0216 others(2): Show |
5 | HG01167.hp1 HG01243.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.27-2149G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148552411 | |||||||
chr5:148552594 | A | G | 1 | a0001c0001t0003g0100 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.27-2332T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148552594 | |||||||
chr5:148552638 | G | A | 280 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0164 others(277): Show |
282 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.27-2376C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148552638 | |||||||
chr5:148552799 | T | C | 1 | a0001c0001t0001g0192 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.27-2537A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148552799 | |||||||
chr5:148553047 | G | A | 9 | a0001c0001t0001g0186 a0001c0001t0001g0216 a0001c0001t0001g0251 others(6): Show |
9 | HG01074.hp1 HG01167.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.27-2785C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148553047 | |||||||
chr5:148553193 | G | T | 3 | a0001c0001t0001g0186 a0001c0001t0001g0216 a0001c0001t0001g0287 |
3 | HG01167.hp1 HG02970.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.27-2931C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148553193 | |||||||
chr5:148553213 | C | CA | 10 | a0001c0001t0001g0183 a0001c0001t0001g0195 a0001c0001t0001g0196 others(7): Show |
10 | HG01884.hp1 HG02257.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.27-2952dupT | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148553213 | |||||||
chr5:148553259 | C | G | 243 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0164 others(240): Show |
246 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(243): Show |
intron_variant | MODIFIER | c.27-2997G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148553259 | |||||||
chr5:148553333 | T | C | 6 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0269 others(3): Show |
6 | HG01074.hp1 HG02615.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.27-3071A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148553333 | |||||||
chr5:148553440 | G | A | 1 | a0001c0006t0003g0110 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.27-3178C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148553440 | |||||||
chr5:148553448 | G | T | 6 | a0001c0001t0001g0193 a0001c0001t0001g0199 a0001c0001t0003g0090 others(3): Show |
6 | HG02258.hp1 HG03041.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.27-3186C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148553448 | |||||||
chr5:148553563 | A | G | 3 | a0001c0001t0003g0102 a0001c0001t0011g0103 a0001c0001t0011g0107 |
3 | HG01496.hp2 HG02922.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.27-3301T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148553563 | |||||||
chr5:148553588 | T | C | 2 | a0001c0001t0002g0052 a0001c0001t0003g0087 |
2 | HG00673.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.27-3326A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148553588 | |||||||
chr5:148553624 | C | T | 4 | a0001c0001t0008g0134 a0001c0001t0008g0135 a0001c0001t0018g0104 others(1): Show |
4 | HG01884.hp2 HG03209.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.27-3362G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148553624 | |||||||
chr5:148553703 | A | C | 104 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0185 others(101): Show |
105 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.27-3441T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148553703 | |||||||
chr5:148553848 | C | T | 1 | a0002c0003t0013g0194 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.27-3586G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148553848 | |||||||
chr5:148553862 | C | T | 9 | a0001c0001t0001g0186 a0001c0001t0001g0216 a0001c0001t0001g0251 others(6): Show |
9 | HG01074.hp1 HG01167.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.27-3600G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148553862 | |||||||
chr5:148553885 | C | T | 1 | a0001c0001t0002g0079 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.27-3623G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148553885 | |||||||
chr5:148553997 | A | G | 1 | a0001c0001t0001g0269 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.27-3735T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148553997 | |||||||
chr5:148554063 | TTTGTTG | T | 6 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0269 others(3): Show |
6 | HG01074.hp1 HG02615.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.27-3807_27-3802del others(6): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148554063 | |||||||
chr5:148554088 | T | G | 5 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0190 others(2): Show |
6 | HG01891.hp1 HG02818.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.27-3826A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148554088 | |||||||
chr5:148554090 | T | G | 3 | a0001c0001t0001g0249 a0001c0001t0001g0253 a0001c0001t0002g0043 |
3 | HG00597.hp2 HG02027.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.27-3828A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148554090 | |||||||
chr5:148554239 | C | T | 3 | a0001c0001t0001g0306 a0001c0001t0009g0156 a0002c0003t0019g0123 |
3 | HG02559.hp1 HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.27-3977G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148554239 | |||||||
chr5:148554317 | C | T | 7 | a0001c0001t0001g0185 a0001c0001t0001g0187 a0001c0001t0001g0188 others(4): Show |
7 | HG01069.hp2 HG01071.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.27-4055G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148554317 | |||||||
chr5:148554502 | A | G | 1 | a0001c0001t0002g0047 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.27-4240T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148554502 | |||||||
chr5:148554511 | A | G | 2 | a0001c0001t0003g0122 a0001c0001t0003g0129 |
2 | NA18981.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.27-4249T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148554511 | |||||||
chr5:148554569 | C | T | 1 | a0001c0001t0005g0138 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.27-4307G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148554569 | |||||||
chr5:148554606 | G | A | 6 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0269 others(3): Show |
6 | HG01074.hp1 HG02615.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.27-4344C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148554606 | |||||||
chr5:148554703 | A | G | 1 | a0001c0008t0001g0159 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.27-4441T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148554703 | |||||||
chr5:148554752 | T | C | 7 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0190 others(4): Show |
8 | HG00673.hp1 HG01891.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.27-4490A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148554752 | |||||||
chr5:148554982 | A | C | 1 | a0001c0001t0001g0176 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.27-4720T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148554982 | |||||||
chr5:148555057 | T | A | 1 | a0001c0001t0001g0182 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.27-4795A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148555057 | |||||||
chr5:148555164 | C | T | 95 | a0001c0001t0001g0185 a0001c0001t0001g0187 a0001c0001t0001g0188 others(92): Show |
95 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.27-4902G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148555164 | |||||||
chr5:148555463 | A | G | 1 | a0001c0006t0003g0110 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.27-5201T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148555463 | |||||||
chr5:148555589 | C | T | 2 | a0001c0001t0002g0052 a0001c0001t0003g0087 |
2 | HG00673.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.27-5327G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148555589 | |||||||
chr5:148555616 | A | G | 1 | a0001c0001t0002g0077 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.27-5354T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148555616 | |||||||
chr5:148555620 | G | A | 1 | a0001c0002t0003g0094 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.27-5358C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148555620 | |||||||
chr5:148555793 | A | G | 1 | a0001c0001t0006g0200 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.27-5531T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148555793 | |||||||
chr5:148555946 | T | TCA | 19 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0190 others(16): Show |
20 | HG01074.hp1 HG01884.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.27-5686_27-5685dup others(2): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148555946 | |||||||
chr5:148555946 | T | TCACA | 4 | a0001c0001t0002g0052 a0001c0001t0003g0087 a0001c0001t0021g0106 others(1): Show |
4 | HG00673.hp1 HG02451.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.27-5688_27-5685dup others(4): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148555946 | |||||||
chr5:148555946 | T | TCACACA | 83 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(80): Show |
83 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.27-5690_27-5685dup others(6): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148555946 | |||||||
chr5:148555946 | T | TCACACAC others(1): Show |
8 | a0001c0001t0001g0192 a0001c0001t0002g0063 a0001c0001t0009g0157 others(5): Show |
8 | HG00621.hp2 HG02145.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.27-5692_27-5685dup others(8): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148555946 | |||||||
chr5:148555946 | T | TCACACAC others(3): Show |
1 | a0001c0002t0001g0162 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.27-5694_27-5685dup others(10): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148555946 | |||||||
chr5:148555946 | T | TCACACAC others(5): Show |
1 | a0001c0002t0008g0136 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.27-5696_27-5685dup others(12): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148555946 | |||||||
chr5:148555946 | T | TCTCACA | 5 | a0001c0001t0001g0202 a0001c0001t0001g0218 a0001c0001t0001g0219 others(2): Show |
5 | HG01243.hp2 HG02572.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.27-5685_27-5684ins others(6): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148555946 | |||||||
chr5:148555968 | ACACT | A | 6 | a0001c0001t0002g0025 a0001c0001t0002g0057 a0001c0001t0002g0058 others(3): Show |
6 | HG01952.hp1 HG02148.hp2 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.27-5710_27-5707del others(4): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148555968 | |||||||
chr5:148555970 | A | T | 55 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(52): Show |
56 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.27-5708T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148555970 | |||||||
chr5:148555972 | T | A | 2 | a0001c0001t0002g0052 a0001c0001t0003g0087 |
2 | HG00673.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.27-5710A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148555972 | |||||||
chr5:148556315 | C | T | 1 | a0001c0001t0006g0200 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.27-6053G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148556315 | |||||||
chr5:148556322 | A | C | 183 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0177 others(180): Show |
185 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.27-6060T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148556322 | |||||||
chr5:148556327 | A | G | 183 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0177 others(180): Show |
185 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.27-6065T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148556327 | |||||||
chr5:148556557 | G | A | 94 | a0001c0001t0001g0185 a0001c0001t0001g0187 a0001c0001t0001g0188 others(91): Show |
94 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.27-6295C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148556557 | |||||||
chr5:148556715 | T | G | 2 | a0001c0002t0003g0088 a0003c0009t0027g0307 |
2 | HG01243.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.27-6453A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148556715 | |||||||
chr5:148557047 | T | C | 3 | a0001c0001t0001g0306 a0001c0001t0009g0156 a0002c0003t0019g0123 |
3 | HG02559.hp1 HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.27-6785A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148557047 | |||||||
chr5:148557070 | C | T | 1 | a0001c0002t0008g0137 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.27-6808G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148557070 | |||||||
chr5:148557300 | G | A | 94 | a0001c0001t0001g0185 a0001c0001t0001g0187 a0001c0001t0001g0188 others(91): Show |
94 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.27-7038C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148557300 | |||||||
chr5:148557365 | AT | A | 61 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(58): Show |
62 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.27-7104delA | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148557365 | |||||||
chr5:148557462 | C | T | 1 | a0001c0001t0001g0281 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.27-7200G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148557462 | |||||||
chr5:148557562 | G | C | 1 | a0001c0001t0001g0238 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.27-7300C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148557562 | |||||||
chr5:148557787 | A | G | 2 | a0001c0001t0001g0243 a0001c0001t0010g0086 |
2 | HG02723.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.27-7525T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148557787 | |||||||
chr5:148557905 | A | C | 191 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0177 others(188): Show |
193 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.27-7643T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148557905 | |||||||
chr5:148557921 | C | A | 2 | a0001c0001t0001g0176 a0001c0001t0006g0175 |
2 | HG03017.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.27-7659G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148557921 | |||||||
chr5:148558004 | T | A | 68 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(65): Show |
69 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.27-7742A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148558004 | |||||||
chr5:148558070 | A | G | 1 | a0001c0001t0010g0086 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.27-7808T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148558070 | |||||||
chr5:148558179 | AAC | A | 9 | a0001c0001t0001g0161 a0001c0001t0001g0171 a0001c0001t0001g0176 others(6): Show |
9 | HG00738.hp2 HG02300.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.27-7919_27-7918del others(2): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148558179 | |||||||
chr5:148558221 | G | C | 1 | a0001c0001t0003g0087 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.27-7959C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148558221 | |||||||
chr5:148558235 | T | C | 9 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0251 others(6): Show |
9 | HG00140.hp1 HG01074.hp1 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.27-7973A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148558235 | |||||||
chr5:148558405 | C | G | 1 | a0001c0001t0001g0279 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.27-8143G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148558405 | |||||||
chr5:148558556 | T | C | 6 | a0001c0001t0001g0198 a0001c0001t0003g0114 a0001c0001t0003g0115 others(3): Show |
6 | HG02257.hp1 HG02451.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.27-8294A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148558556 | |||||||
chr5:148558593 | C | T | 1 | a0001c0001t0005g0143 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.27-8331G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148558593 | |||||||
chr5:148558710 | C | T | 2 | a0001c0001t0001g0248 a0001c0001t0001g0301 |
2 | HG00738.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.27-8448G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148558710 | |||||||
chr5:148559004 | C | T | 15 | a0001c0001t0001g0183 a0001c0001t0001g0195 a0001c0001t0001g0196 others(12): Show |
15 | HG01496.hp2 HG01884.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.27-8742G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148559004 | |||||||
chr5:148559289 | G | T | 3 | a0001c0001t0001g0183 a0001c0001t0001g0195 a0001c0001t0001g0196 |
3 | HG02486.hp1 HG02970.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.27-9027C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148559289 | |||||||
chr5:148559292 | G | A | 1 | a0001c0001t0009g0155 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.27-9030C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148559292 | |||||||
chr5:148559309 | G | T | 2 | a0001c0001t0002g0057 a0001c0001t0002g0058 |
2 | NA18941.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.27-9047C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148559309 | |||||||
chr5:148559399 | A | G | 158 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0177 others(155): Show |
160 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.27-9137T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148559399 | |||||||
chr5:148559454 | T | G | 9 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0251 others(6): Show |
9 | HG00140.hp1 HG01074.hp1 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.27-9192A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148559454 | |||||||
chr5:148559539 | T | C | 3 | a0001c0001t0002g0063 a0001c0001t0002g0072 a0001c0001t0002g0076 |
3 | HG00621.hp2 HG02056.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.27-9277A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148559539 | |||||||
chr5:148559604 | A | G | 5 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0190 others(2): Show |
6 | HG01891.hp1 HG02818.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.27-9342T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148559604 | |||||||
chr5:148559636 | C | T | 2 | a0001c0001t0008g0134 a0001c0001t0008g0135 |
2 | NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.27-9374G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148559636 | |||||||
chr5:148559642 | G | A | 2 | a0001c0001t0001g0302 a0001c0001t0003g0117 |
2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.27-9380C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148559642 | |||||||
chr5:148559667 | A | G | 1 | a0001c0001t0001g0193 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.27-9405T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148559667 | |||||||
chr5:148559677 | C | T | 64 | a0001c0001t0001g0179 a0001c0001t0001g0201 a0001c0001t0001g0204 others(61): Show |
65 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.27-9415G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148559677 | |||||||
chr5:148559784 | C | T | 1 | a0001c0001t0021g0106 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.27-9522G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148559784 | |||||||
chr5:148560135 | A | G | 3 | a0001c0001t0001g0183 a0001c0001t0001g0195 a0001c0001t0001g0196 |
3 | HG02486.hp1 HG02970.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.27-9873T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148560135 | |||||||
chr5:148560161 | C | T | 82 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0190 others(79): Show |
83 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.27-9899G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148560161 | |||||||
chr5:148560196 | CT | C | 19 | a0001c0001t0001g0179 a0001c0001t0001g0183 a0001c0001t0001g0185 others(16): Show |
19 | HG01069.hp2 HG01071.hp2 HG01496.hp2 others(16): Show |
intron_variant | MODIFIER | c.27-9935delA | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148560196 | |||||||
chr5:148560196 | CTT | C | 7 | a0001c0001t0001g0228 a0001c0001t0001g0254 a0001c0001t0001g0266 others(4): Show |
7 | HG02080.hp2 NA18943.hp1 NA18945.hp2 others(4): Show |
intron_variant | MODIFIER | c.27-9936_27-9935del others(2): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148560196 | |||||||
chr5:148560204 | TTA | T | 55 | a0001c0001t0001g0171 a0001c0001t0001g0198 a0001c0001t0001g0201 others(52): Show |
56 | HG00423.hp1 HG00438.hp2 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.27-9944_27-9943del others(2): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148560204 | |||||||
chr5:148560204 | TTAA | T | 13 | a0001c0001t0001g0249 a0001c0001t0001g0271 a0001c0001t0001g0292 others(10): Show |
13 | HG00099.hp2 HG00323.hp1 HG00738.hp1 others(10): Show |
intron_variant | MODIFIER | c.27-9945_27-9943del others(3): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148560204 | |||||||
chr5:148560205 | T | A | 8 | a0001c0001t0001g0266 a0001c0001t0001g0277 a0001c0001t0002g0010 others(5): Show |
8 | HG02155.hp1 HG02155.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.27-9943A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148560205 | |||||||
chr5:148560205 | T | TA | 11 | a0001c0001t0001g0164 a0001c0001t0001g0230 a0001c0001t0001g0284 others(8): Show |
11 | HG00099.hp1 HG00408.hp2 HG00558.hp1 others(8): Show |
intron_variant | MODIFIER | c.27-9944dupT | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148560205 | |||||||
chr5:148560205 | TA | T | 29 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0173 others(26): Show |
30 | HG00323.hp2 HG00738.hp2 HG01169.hp2 others(27): Show |
intron_variant | MODIFIER | c.27-9944delT | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148560205 | |||||||
chr5:148560205 | TAA | T | 68 | a0001c0001t0001g0176 a0001c0001t0001g0202 a0001c0001t0001g0211 others(65): Show |
68 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.27-9945_27-9944del others(2): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148560205 | |||||||
chr5:148560205 | TAAA | T | 11 | a0001c0001t0001g0192 a0001c0001t0001g0302 a0001c0001t0002g0020 others(8): Show |
11 | HG01981.hp1 HG02809.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.27-9946_27-9944del others(3): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148560205 | |||||||
chr5:148560205 | TAAAA | T | 11 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0186 others(8): Show |
11 | HG00140.hp1 HG01361.hp2 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.27-9947_27-9944del others(4): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148560205 | |||||||
chr5:148560207 | A | T | 2 | a0001c0001t0007g0051 a0001c0001t0012g0205 |
2 | HG02647.hp1 NA18949.hp1 |
intron_variant | MODIFIER | c.27-9945T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148560207 | |||||||
chr5:148560208 | A | T | 60 | a0001c0001t0001g0202 a0001c0001t0001g0211 a0001c0001t0001g0213 others(57): Show |
60 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.27-9946T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148560208 | |||||||
chr5:148560209 | A | T | 8 | a0001c0001t0001g0302 a0001c0001t0002g0020 a0001c0001t0003g0096 others(5): Show |
8 | HG01981.hp1 HG02809.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.27-9947T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148560209 | |||||||
chr5:148560210 | A | T | 3 | a0001c0001t0001g0186 a0001c0001t0001g0216 a0001c0001t0003g0097 |
3 | HG02970.hp1 HG03579.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.27-9948T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148560210 | |||||||
chr5:148560211 | A | T | 1 | a0001c0001t0001g0287 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.27-9949T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148560211 | |||||||
chr5:148560215 | A | G | 1 | a0003c0009t0027g0307 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.27-9953T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148560215 | |||||||
chr5:148560265 | A | G | 1 | a0001c0001t0003g0087 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.27-10003T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148560265 | |||||||
chr5:148560365 | A | G | 1 | a0001c0002t0003g0088 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.27-10103T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148560365 | |||||||
chr5:148560479 | C | T | 96 | a0001c0001t0001g0179 a0001c0001t0001g0183 a0001c0001t0001g0185 others(93): Show |
97 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.27-10217G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148560479 | |||||||
chr5:148560490 | C | A | 14 | a0001c0001t0001g0202 a0001c0001t0001g0211 a0001c0001t0001g0213 others(11): Show |
14 | HG01243.hp2 HG02055.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.27-10228G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148560490 | |||||||
chr5:148560592 | T | C | 1 | a0001c0001t0001g0181 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.27-10330A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148560592 | |||||||
chr5:148560613 | A | G | 1 | a0001c0001t0006g0175 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.27-10351T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148560613 | |||||||
chr5:148560699 | A | T | 5 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0190 others(2): Show |
6 | HG01891.hp1 HG02818.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.27-10437T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148560699 | |||||||
chr5:148561194 | A | C | 1 | a0001c0001t0002g0027 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.27-10932T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148561194 | |||||||
chr5:148561250 | A | T | 1 | a0001c0001t0001g0238 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.27-10988T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148561250 | |||||||
chr5:148561482 | C | G | 2 | a0001c0001t0001g0176 a0001c0001t0006g0175 |
2 | HG03017.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.27-11220G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148561482 | |||||||
chr5:148561492 | G | A | 91 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0177 others(88): Show |
92 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.27-11230C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148561492 | |||||||
chr5:148561596 | G | A | 1 | a0001c0001t0001g0243 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.27-11334C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148561596 | |||||||
chr5:148561625 | A | AT | 7 | a0001c0001t0003g0100 a0001c0002t0001g0160 a0001c0002t0001g0162 others(4): Show |
7 | HG02145.hp2 HG02451.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.27-11364dupA | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148561625 | |||||||
chr5:148561625 | AT | A | 23 | a0001c0001t0001g0183 a0001c0001t0001g0185 a0001c0001t0001g0187 others(20): Show |
23 | HG01069.hp2 HG01071.hp2 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.27-11364delA | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148561625 | |||||||
chr5:148561783 | T | C | 1 | a0001c0006t0003g0110 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.27-11521A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148561783 | |||||||
chr5:148561804 | C | T | 1 | a0001c0001t0001g0228 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.27-11542G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148561804 | |||||||
chr5:148561833 | T | A | 1 | a0001c0001t0006g0200 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.27-11571A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148561833 | |||||||
chr5:148561865 | C | T | 1 | a0001c0001t0010g0086 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.27-11603G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148561865 | |||||||
chr5:148561938 | C | G | 80 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0190 others(77): Show |
81 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.27-11676G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148561938 | |||||||
chr5:148562035 | C | T | 2 | a0001c0001t0003g0111 a0001c0001t0004g0286 |
2 | HG00558.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.27-11773G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148562035 | |||||||
chr5:148562204 | T | G | 6 | a0001c0001t0001g0198 a0001c0001t0003g0114 a0001c0001t0003g0115 others(3): Show |
6 | HG02257.hp1 HG02451.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.27-11942A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148562204 | |||||||
chr5:148562282 | G | C | 208 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0171 others(205): Show |
210 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.27-12020C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148562282 | |||||||
chr5:148562291 | C | T | 1 | a0001c0001t0001g0260 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.27-12029G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148562291 | |||||||
chr5:148562437 | C | T | 1 | a0001c0001t0002g0026 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.27-12175G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148562437 | |||||||
chr5:148562447 | C | T | 2 | a0001c0001t0002g0057 a0001c0001t0002g0058 |
2 | NA18941.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.27-12185G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148562447 | |||||||
chr5:148562470 | C | T | 1 | a0001c0001t0010g0086 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.27-12208G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148562470 | |||||||
chr5:148562588 | A | G | 1 | a0001c0006t0003g0110 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.27-12326T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148562588 | |||||||
chr5:148562593 | A | G | 1 | a0001c0001t0003g0100 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.27-12331T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148562593 | |||||||
chr5:148562675 | T | C | 197 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0171 others(194): Show |
199 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.27-12413A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148562675 | |||||||
chr5:148562841 | A | C | 64 | a0001c0001t0001g0179 a0001c0001t0001g0201 a0001c0001t0001g0204 others(61): Show |
65 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.27-12579T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148562841 | |||||||
chr5:148562959 | A | G | 17 | a0001c0001t0001g0172 a0001c0001t0001g0181 a0001c0001t0002g0005 others(14): Show |
17 | HG00408.hp2 HG00558.hp2 HG02080.hp1 others(14): Show |
intron_variant | MODIFIER | c.27-12697T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148562959 | |||||||
chr5:148563187 | G | A | 2 | a0001c0001t0002g0061 a0001c0001t0002g0066 |
2 | HG03831.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.27-12925C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148563187 | |||||||
chr5:148563381 | C | T | 1 | a0001c0001t0003g0087 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.27-13119G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148563381 | |||||||
chr5:148563430 | T | C | 64 | a0001c0001t0001g0179 a0001c0001t0001g0201 a0001c0001t0001g0204 others(61): Show |
65 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.27-13168A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148563430 | |||||||
chr5:148563442 | C | T | 182 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0177 others(179): Show |
184 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.27-13180G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148563442 | |||||||
chr5:148563452 | C | G | 2 | a0001c0001t0001g0210 a0001c0001t0001g0290 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.27-13190G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148563452 | |||||||
chr5:148563609 | C | T | 45 | a0001c0001t0001g0179 a0001c0001t0001g0204 a0001c0001t0001g0228 others(42): Show |
46 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(43): Show |
intron_variant | MODIFIER | c.27-13347G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148563609 | |||||||
chr5:148563924 | A | ATGAC | 18 | a0001c0001t0001g0202 a0001c0001t0001g0211 a0001c0001t0001g0213 others(15): Show |
18 | HG01243.hp2 HG02055.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.27-13666_27-13663d others(6): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148563924 | |||||||
chr5:148563936 | A | C | 80 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0190 others(77): Show |
81 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.27-13674T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148563936 | |||||||
chr5:148564159 | T | C | 2 | a0001c0001t0008g0134 a0001c0001t0008g0135 |
2 | NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.27-13897A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148564159 | |||||||
chr5:148564182 | A | T | 92 | a0001c0001t0001g0179 a0001c0001t0001g0183 a0001c0001t0001g0185 others(89): Show |
93 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.27-13920T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148564182 | |||||||
chr5:148564206 | T | C | 185 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0177 others(182): Show |
187 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.27-13944A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148564206 | |||||||
chr5:148564223 | G | T | 1 | a0001c0001t0001g0207 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.27-13961C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148564223 | |||||||
chr5:148564349 | C | T | 2 | a0001c0001t0002g0072 a0001c0001t0002g0076 |
2 | HG02056.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.27-14087G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148564349 | |||||||
chr5:148564350 | G | A | 1 | a0001c0001t0001g0192 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.27-14088C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148564350 | |||||||
chr5:148564434 | C | A | 1 | a0001c0001t0002g0053 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.27-14172G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148564434 | |||||||
chr5:148564798 | G | A | 1 | a0001c0001t0025g0270 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.27-14536C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148564798 | |||||||
chr5:148564849 | C | T | 1 | a0001c0001t0002g0070 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.27-14587G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148564849 | |||||||
chr5:148564924 | G | A | 185 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0177 others(182): Show |
187 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.27-14662C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148564924 | |||||||
chr5:148564975 | T | C | 1 | a0001c0001t0001g0172 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.27-14713A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148564975 | |||||||
chr5:148565052 | G | A | 1 | a0001c0001t0001g0254 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.27-14790C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148565052 | |||||||
chr5:148565108 | TA | T | 17 | a0001c0001t0001g0186 a0001c0001t0001g0202 a0001c0001t0001g0208 others(14): Show |
17 | HG00323.hp1 HG01167.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.27-14847delT | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148565108 | |||||||
chr5:148565108 | TAA | T | 87 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0177 others(84): Show |
88 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.27-14848_27-14847d others(4): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148565108 | |||||||
chr5:148565278 | T | C | 1 | a0001c0001t0010g0086 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.27-15016A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148565278 | |||||||
chr5:148565298 | T | A | 1 | a0001c0001t0003g0098 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.27-15036A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148565298 | |||||||
chr5:148565356 | C | T | 9 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0251 others(6): Show |
9 | HG00140.hp1 HG01074.hp1 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.27-15094G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148565356 | |||||||
chr5:148565501 | T | C | 4 | a0001c0001t0001g0202 a0001c0001t0001g0218 a0001c0001t0001g0219 others(1): Show |
4 | HG02572.hp1 HG02717.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.27-15239A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148565501 | |||||||
chr5:148565585 | G | A | 1 | a0001c0001t0010g0086 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.27-15323C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148565585 | |||||||
chr5:148565734 | G | A | 1 | a0001c0001t0003g0113 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.27-15472C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148565734 | |||||||
chr5:148565744 | G | A | 1 | a0001c0001t0001g0269 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.27-15482C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148565744 | |||||||
chr5:148565841 | C | T | 1 | a0001c0001t0009g0155 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.27-15579G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148565841 | |||||||
chr5:148565873 | G | A | 17 | a0001c0001t0001g0183 a0001c0001t0001g0185 a0001c0001t0001g0187 others(14): Show |
17 | HG01069.hp2 HG01071.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.27-15611C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148565873 | |||||||
chr5:148565881 | T | C | 6 | a0001c0001t0001g0198 a0001c0001t0003g0114 a0001c0001t0003g0115 others(3): Show |
6 | HG02257.hp1 HG02451.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.27-15619A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148565881 | |||||||
chr5:148566047 | A | T | 1 | a0001c0001t0010g0086 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.27-15785T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148566047 | |||||||
chr5:148566278 | A | C | 1 | a0001c0001t0005g0139 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.27-16016T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148566278 | |||||||
chr5:148566717 | T | C | 1 | a0001c0002t0008g0137 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.27-16455A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148566717 | |||||||
chr5:148566782 | C | T | 2 | a0001c0001t0001g0202 a0001c0001t0026g0184 |
2 | HG01884.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.27-16520G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148566782 | |||||||
chr5:148566853 | C | T | 1 | a0001c0001t0001g0217 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.27-16591G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148566853 | |||||||
chr5:148566877 | T | A | 1 | a0001c0001t0002g0013 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.27-16615A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148566877 | |||||||
chr5:148567398 | T | C | 14 | a0001c0001t0001g0202 a0001c0001t0001g0211 a0001c0001t0001g0213 others(11): Show |
14 | HG01243.hp2 HG02055.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.27-17136A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148567398 | |||||||
chr5:148567463 | A | G | 82 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0190 others(79): Show |
83 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.27-17201T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148567463 | |||||||
chr5:148567483 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.27-17221G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148567483 | |||||||
chr5:148567602 | G | T | 2 | a0001c0001t0008g0134 a0001c0001t0008g0135 |
2 | NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.27-17340C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148567602 | |||||||
chr5:148567650 | G | A | 6 | a0001c0001t0001g0198 a0001c0001t0003g0114 a0001c0001t0003g0115 others(3): Show |
6 | HG02257.hp1 HG02451.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.27-17388C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148567650 | |||||||
chr5:148567659 | T | G | 1 | a0001c0001t0002g0010 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.27-17397A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148567659 | |||||||
chr5:148567725 | C | T | 63 | a0001c0001t0001g0179 a0001c0001t0001g0201 a0001c0001t0001g0204 others(60): Show |
64 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.27-17463G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148567725 | |||||||
chr5:148567860 | T | C | 1 | a0001c0001t0004g0255 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.27-17598A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148567860 | |||||||
chr5:148567904 | C | G | 3 | a0001c0001t0001g0186 a0001c0001t0001g0216 a0001c0001t0001g0287 |
3 | HG01167.hp1 HG02970.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.27-17642G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148567904 | |||||||
chr5:148567921 | G | A | 91 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0177 others(88): Show |
92 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.27-17659C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148567921 | |||||||
chr5:148567931 | G | A | 1 | a0002c0003t0013g0194 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.27-17669C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148567931 | |||||||
chr5:148568020 | G | A | 1 | a0001c0001t0026g0184 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.27-17758C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148568020 | |||||||
chr5:148568431 | T | C | 10 | a0001c0001t0001g0161 a0001c0001t0001g0171 a0001c0001t0001g0176 others(7): Show |
10 | HG00738.hp2 HG02300.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.27-18169A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148568431 | |||||||
chr5:148568441 | T | C | 2 | a0001c0001t0001g0176 a0001c0001t0006g0175 |
2 | HG03017.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.27-18179A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148568441 | |||||||
chr5:148568548 | T | C | 1 | a0001c0001t0001g0243 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.27-18286A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148568548 | |||||||
chr5:148568711 | A | G | 129 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0171 others(126): Show |
130 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.27-18449T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148568711 | |||||||
chr5:148568750 | T | A | 1 | a0001c0001t0001g0273 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.27-18488A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148568750 | |||||||
chr5:148568763 | G | A | 5 | a0001c0001t0001g0234 a0001c0001t0001g0264 a0001c0001t0001g0267 others(2): Show |
5 | HG00423.hp1 NA18942.hp1 NA18955.hp2 others(2): Show |
intron_variant | MODIFIER | c.27-18501C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148568763 | |||||||
chr5:148568795 | A | G | 1 | a0001c0001t0001g0261 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.27-18533T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148568795 | |||||||
chr5:148568983 | G | A | 63 | a0001c0001t0001g0179 a0001c0001t0001g0201 a0001c0001t0001g0204 others(60): Show |
64 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.27-18721C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148568983 | |||||||
chr5:148569024 | T | G | 1 | a0001c0001t0003g0087 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.27-18762A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148569024 | |||||||
chr5:148569038 | A | G | 9 | a0001c0001t0001g0186 a0001c0001t0001g0198 a0001c0001t0001g0216 others(6): Show |
9 | HG01167.hp1 HG02257.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.27-18776T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148569038 | |||||||
chr5:148569077 | G | GT | 13 | a0001c0001t0001g0161 a0001c0001t0001g0171 a0001c0001t0001g0176 others(10): Show |
13 | HG00738.hp2 HG02055.hp2 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.27-18816dupA | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148569077 | |||||||
chr5:148569077 | GT | G | 14 | a0001c0001t0001g0185 a0001c0001t0001g0187 a0001c0001t0001g0188 others(11): Show |
14 | HG01069.hp2 HG01071.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.27-18816delA | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148569077 | |||||||
chr5:148569331 | G | A | 1 | a0001c0001t0003g0101 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.27-19069C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148569331 | |||||||
chr5:148569346 | G | A | 1 | a0001c0001t0005g0152 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.27-19084C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148569346 | |||||||
chr5:148569356 | G | A | 1 | a0001c0001t0021g0106 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.27-19094C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148569356 | |||||||
chr5:148569493 | T | C | 81 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0190 others(78): Show |
82 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.27-19231A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148569493 | |||||||
chr5:148569594 | T | C | 1 | a0001c0001t0007g0065 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.27-19332A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148569594 | |||||||
chr5:148569768 | T | G | 1 | a0001c0001t0005g0152 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.27-19506A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148569768 | |||||||
chr5:148569815 | C | A | 9 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0251 others(6): Show |
9 | HG00140.hp1 HG01074.hp1 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.27-19553G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148569815 | |||||||
chr5:148569829 | A | G | 1 | a0001c0001t0001g0171 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.27-19567T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148569829 | |||||||
chr5:148569831 | C | A | 1 | a0001c0001t0001g0243 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.27-19569G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148569831 | |||||||
chr5:148569886 | T | C | 1 | a0001c0006t0003g0110 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.27-19624A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148569886 | |||||||
chr5:148570048 | T | C | 115 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0177 others(112): Show |
116 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.27-19786A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148570048 | |||||||
chr5:148570408 | A | G | 111 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0171 others(108): Show |
112 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.27-20146T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148570408 | |||||||
chr5:148570591 | G | A | 9 | a0001c0001t0001g0161 a0001c0001t0001g0171 a0001c0001t0001g0176 others(6): Show |
9 | HG00738.hp2 HG02300.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.27-20329C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148570591 | |||||||
chr5:148570611 | T | C | 112 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0171 others(109): Show |
113 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.27-20349A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148570611 | |||||||
chr5:148570833 | GGTTTTT | G | 63 | a0001c0001t0001g0179 a0001c0001t0001g0201 a0001c0001t0001g0204 others(60): Show |
64 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.27-20577_27-20572d others(8): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148570833 | |||||||
chr5:148570915 | A | C | 79 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0190 others(76): Show |
80 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.27-20653T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148570915 | |||||||
chr5:148570995 | G | A | 1 | a0001c0001t0004g0305 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.27-20733C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148570995 | |||||||
chr5:148571515 | C | T | 9 | a0001c0001t0001g0161 a0001c0001t0001g0171 a0001c0001t0001g0176 others(6): Show |
9 | HG00738.hp2 HG02300.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.27-21253G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148571515 | |||||||
chr5:148571616 | T | G | 1 | a0001c0001t0014g0004 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.27-21354A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148571616 | |||||||
chr5:148571661 | T | C | 10 | a0001c0001t0001g0161 a0001c0001t0001g0171 a0001c0001t0001g0176 others(7): Show |
10 | HG00738.hp2 HG02300.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.27-21399A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148571661 | |||||||
chr5:148571683 | T | A | 1 | a0001c0001t0009g0155 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.27-21421A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148571683 | |||||||
chr5:148571800 | C | T | 2 | a0001c0001t0001g0302 a0001c0001t0003g0117 |
2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.27-21538G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148571800 | |||||||
chr5:148571813 | T | C | 1 | a0001c0001t0010g0086 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.27-21551A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148571813 | |||||||
chr5:148571904 | A | C | 2 | a0001c0001t0001g0271 a0001c0001t0015g0014 |
2 | HG01981.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.27-21642T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148571904 | |||||||
chr5:148572289 | C | T | 1 | a0001c0001t0001g0283 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.27-22027G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148572289 | |||||||
chr5:148572520 | T | A | 2 | a0001c0001t0005g0139 a0001c0001t0005g0142 |
2 | HG02698.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.27-22258A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148572520 | |||||||
chr5:148572634 | A | T | 1 | a0001c0001t0002g0036 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.27-22372T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148572634 | |||||||
chr5:148572829 | T | G | 1 | a0001c0001t0021g0106 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.27-22567A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148572829 | |||||||
chr5:148572976 | T | C | 101 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0171 others(98): Show |
102 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.27-22714A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148572976 | |||||||
chr5:148573049 | C | T | 2 | a0001c0004t0001g0242 a0001c0004t0003g0118 |
2 | HG02300.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.27-22787G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148573049 | |||||||
chr5:148573158 | T | A | 1 | a0001c0001t0005g0143 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.27-22896A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148573158 | |||||||
chr5:148573244 | G | A | 1 | a0001c0002t0008g0137 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.27-22982C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148573244 | |||||||
chr5:148573391 | T | C | 1 | a0001c0001t0003g0101 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.27-23129A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148573391 | |||||||
chr5:148573452 | C | T | 10 | a0001c0001t0001g0161 a0001c0001t0001g0171 a0001c0001t0001g0176 others(7): Show |
10 | HG00738.hp2 HG02300.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.27-23190G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148573452 | |||||||
chr5:148573472 | G | T | 5 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0304 others(2): Show |
5 | HG02615.hp2 HG02622.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.27-23210C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148573472 | |||||||
chr5:148573550 | C | T | 73 | a0001c0001t0001g0202 a0001c0001t0001g0211 a0001c0001t0001g0213 others(70): Show |
73 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.27-23288G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148573550 | |||||||
chr5:148573561 | T | C | 7 | a0001c0001t0001g0164 a0001c0001t0004g0002 a0001c0001t0004g0165 others(4): Show |
8 | NA18947.hp2 NA18963.hp1 NA18964.hp1 others(5): Show |
intron_variant | MODIFIER | c.27-23299A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148573561 | |||||||
chr5:148573646 | A | T | 1 | a0001c0006t0003g0110 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.27-23384T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148573646 | |||||||
chr5:148573684 | T | C | 90 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0177 others(87): Show |
91 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.27-23422A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148573684 | |||||||
chr5:148573704 | A | G | 1 | a0001c0001t0003g0087 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.27-23442T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148573704 | |||||||
chr5:148573808 | G | A | 1 | a0001c0001t0001g0224 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.27-23546C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148573808 | |||||||
chr5:148573979 | C | T | 6 | a0001c0001t0002g0025 a0001c0001t0002g0057 a0001c0001t0002g0058 others(3): Show |
6 | HG01952.hp1 HG02148.hp2 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.27-23717G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148573979 | |||||||
chr5:148573982 | G | A | 63 | a0001c0001t0001g0179 a0001c0001t0001g0201 a0001c0001t0001g0204 others(60): Show |
64 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.27-23720C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148573982 | |||||||
chr5:148574036 | C | T | 11 | a0001c0001t0001g0161 a0001c0001t0001g0171 a0001c0001t0001g0176 others(8): Show |
11 | HG00738.hp2 HG02300.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.27-23774G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148574036 | |||||||
chr5:148574390 | G | GCT | 81 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0190 others(78): Show |
82 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.27-24130_27-24129d others(4): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148574390 | |||||||
chr5:148574392 | T | G | 10 | a0001c0001t0001g0161 a0001c0001t0001g0171 a0001c0001t0001g0176 others(7): Show |
10 | HG00738.hp2 HG02300.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.27-24130A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148574392 | |||||||
chr5:148574394 | T | G | 9 | a0001c0001t0001g0161 a0001c0001t0001g0171 a0001c0001t0001g0176 others(6): Show |
9 | HG00738.hp2 HG02300.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.27-24132A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148574394 | |||||||
chr5:148574423 | C | T | 1 | a0001c0001t0003g0087 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.27-24161G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148574423 | |||||||
chr5:148574424 | G | A | 1 | a0001c0001t0001g0262 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.27-24162C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148574424 | |||||||
chr5:148574463 | A | G | 2 | a0001c0001t0001g0275 a0001c0001t0001g0289 |
2 | HG01516.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.27-24201T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148574463 | |||||||
chr5:148574573 | T | C | 9 | a0001c0001t0001g0186 a0001c0001t0001g0198 a0001c0001t0001g0216 others(6): Show |
9 | HG01167.hp1 HG02257.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.27-24311A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148574573 | |||||||
chr5:148574616 | T | C | 9 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0251 others(6): Show |
9 | HG00140.hp1 HG01074.hp1 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.27-24354A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148574616 | |||||||
chr5:148574623 | G | C | 63 | a0001c0001t0001g0179 a0001c0001t0001g0201 a0001c0001t0001g0204 others(60): Show |
64 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.27-24361C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148574623 | |||||||
chr5:148574660 | T | C | 1 | a0001c0001t0003g0087 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.27-24398A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148574660 | |||||||
chr5:148574683 | C | T | 1 | a0001c0001t0003g0087 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.27-24421G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148574683 | |||||||
chr5:148574717 | A | G | 111 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0171 others(108): Show |
112 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.27-24455T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148574717 | |||||||
chr5:148574756 | C | T | 1 | a0001c0001t0021g0106 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.27-24494G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148574756 | |||||||
chr5:148574805 | G | A | 5 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0190 others(2): Show |
6 | HG01891.hp1 HG02818.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.27-24543C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148574805 | |||||||
chr5:148574848 | A | G | 1 | a0001c0001t0021g0106 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.27-24586T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148574848 | |||||||
chr5:148574922 | A | T | 21 | a0001c0001t0001g0161 a0001c0001t0001g0171 a0001c0001t0001g0176 others(18): Show |
21 | HG00673.hp1 HG00738.hp2 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.27-24660T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148574922 | |||||||
chr5:148575245 | C | T | 1 | a0001c0001t0010g0086 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.27-24983G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148575245 | |||||||
chr5:148575347 | AC | A | 18 | a0001c0001t0001g0183 a0001c0001t0001g0185 a0001c0001t0001g0187 others(15): Show |
18 | HG01069.hp2 HG01071.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.27-25086delG | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148575347 | |||||||
chr5:148575555 | G | A | 1 | a0001c0001t0001g0289 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.27-25293C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148575555 | |||||||
chr5:148575573 | C | T | 9 | a0001c0001t0001g0161 a0001c0001t0001g0171 a0001c0001t0001g0176 others(6): Show |
9 | HG00738.hp2 HG02300.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.27-25311G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148575573 | |||||||
chr5:148575864 | A | G | 7 | a0001c0001t0001g0198 a0001c0001t0001g0216 a0001c0001t0003g0114 others(4): Show |
7 | HG02257.hp1 HG02451.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.27-25602T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148575864 | |||||||
chr5:148575887 | A | T | 1 | a0001c0001t0002g0076 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.27-25625T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148575887 | |||||||
chr5:148576077 | C | T | 1 | a0001c0001t0003g0108 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.27-25815G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148576077 | |||||||
chr5:148576098 | G | A | 1 | a0001c0001t0002g0026 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.27-25836C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148576098 | |||||||
chr5:148576106 | G | A | 1 | a0001c0008t0001g0159 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.27-25844C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148576106 | |||||||
chr5:148576110 | C | CA | 14 | a0001c0001t0001g0180 a0001c0001t0001g0224 a0001c0001t0001g0258 others(11): Show |
14 | HG01361.hp1 HG01891.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.27-25849dupT | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148576110 | |||||||
chr5:148576110 | C | CAAAAAAA others(1): Show |
11 | a0001c0001t0001g0003 a0001c0001t0001g0191 a0001c0001t0001g0243 others(8): Show |
12 | HG00099.hp2 HG02258.hp2 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.27-25856_27-25849d others(10): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148576110 | |||||||
chr5:148576110 | C | CAAAAAAA others(2): Show |
77 | a0001c0001t0001g0173 a0001c0001t0001g0190 a0001c0001t0001g0192 others(74): Show |
78 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.27-25857_27-25849d others(11): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148576110 | |||||||
chr5:148576110 | C | CAAAAAAA others(3): Show |
54 | a0001c0001t0001g0179 a0001c0001t0001g0201 a0001c0001t0001g0213 others(51): Show |
54 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.27-25858_27-25849d others(12): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148576110 | |||||||
chr5:148576110 | C | CAAAAAAA others(4): Show |
2 | a0001c0001t0003g0098 a0001c0001t0006g0200 |
2 | HG02145.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.27-25859_27-25849d others(13): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148576110 | |||||||
chr5:148576110 | C | CAAAAAAA others(5): Show |
2 | a0001c0001t0001g0287 a0001c0001t0010g0086 |
2 | HG01167.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.27-25860_27-25849d others(14): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148576110 | |||||||
chr5:148576110 | C | CAAAAAAA others(6): Show |
2 | a0001c0001t0001g0186 a0001c0001t0001g0216 |
2 | HG02970.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.27-25861_27-25849d others(15): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148576110 | |||||||
chr5:148576110 | CAAAAAAA others(4): Show |
C | 9 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0251 others(6): Show |
9 | HG00140.hp1 HG01074.hp1 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.27-25859_27-25849d others(13): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148576110 | |||||||
chr5:148576119 | A | AAAAAAAA others(3): Show |
2 | a0001c0001t0001g0176 a0001c0001t0006g0175 |
2 | HG03017.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.27-25858_27-25857i others(12): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148576119 | |||||||
chr5:148576119 | A | AAAAAAAA others(2): Show |
7 | a0001c0001t0001g0161 a0001c0001t0001g0171 a0001c0001t0001g0248 others(4): Show |
7 | HG00738.hp2 HG02300.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.27-25858_27-25857i others(11): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148576119 | |||||||
chr5:148576120 | A | AAAAACAA others(2): Show |
16 | a0001c0001t0001g0183 a0001c0001t0001g0185 a0001c0001t0001g0187 others(13): Show |
16 | HG01069.hp2 HG01071.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.27-25859_27-25858i others(11): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148576120 | |||||||
chr5:148576128 | A | AAAAAAAA others(6): Show |
1 | a0001c0001t0024g0154 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.27-25867_27-25866i others(15): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148576128 | |||||||
chr5:148576128 | A | AAAAAAAA others(5): Show |
5 | a0001c0001t0001g0198 a0001c0001t0003g0114 a0001c0001t0003g0115 others(2): Show |
5 | HG02257.hp1 HG02886.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.27-25867_27-25866i others(14): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148576128 | |||||||
chr5:148576134 | C | A | 3 | a0001c0001t0002g0045 a0001c0001t0003g0098 a0001c0001t0005g0150 |
3 | HG01978.hp1 NA18986.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.27-25872G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148576134 | |||||||
chr5:148576243 | A | G | 1 | a0001c0001t0010g0086 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.27-25981T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148576243 | |||||||
chr5:148576391 | T | C | 129 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0171 others(126): Show |
130 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.27-26129A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148576391 | |||||||
chr5:148576491 | T | A | 193 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0171 others(190): Show |
195 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.27-26229A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148576491 | |||||||
chr5:148576738 | A | G | 1 | a0001c0001t0010g0086 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.27-26476T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148576738 | |||||||
chr5:148577390 | A | G | 1 | a0001c0001t0021g0106 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.27-27128T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148577390 | |||||||
chr5:148577412 | T | A | 1 | a0001c0001t0001g0192 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.27-27150A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148577412 | |||||||
chr5:148577586 | G | C | 1 | a0001c0001t0010g0086 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.27-27324C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148577586 | |||||||
chr5:148577671 | A | C | 111 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0171 others(108): Show |
112 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.27-27409T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148577671 | |||||||
chr5:148577727 | A | C | 111 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0171 others(108): Show |
112 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.27-27465T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148577727 | |||||||
chr5:148577755 | A | G | 111 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0171 others(108): Show |
112 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.27-27493T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148577755 | |||||||
chr5:148577781 | C | T | 63 | a0001c0001t0001g0179 a0001c0001t0001g0201 a0001c0001t0001g0204 others(60): Show |
64 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.27-27519G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148577781 | |||||||
chr5:148577842 | G | A | 1 | a0001c0001t0021g0106 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.27-27580C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148577842 | |||||||
chr5:148577843 | A | G | 1 | a0001c0001t0021g0106 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.27-27581T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148577843 | |||||||
chr5:148577944 | C | T | 2 | a0001c0001t0001g0185 a0001c0001t0009g0153 |
2 | HG03453.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.27-27682G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148577944 | |||||||
chr5:148578000 | A | G | 18 | a0001c0001t0001g0202 a0001c0001t0001g0211 a0001c0001t0001g0213 others(15): Show |
18 | HG01243.hp2 HG02055.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.27-27738T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148578000 | |||||||
chr5:148578024 | T | C | 1 | a0001c0001t0021g0106 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.27-27762A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148578024 | |||||||
chr5:148578067 | C | T | 129 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0171 others(126): Show |
130 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.27-27805G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148578067 | |||||||
chr5:148578455 | G | T | 7 | a0001c0001t0001g0294 a0001c0001t0001g0295 a0001c0001t0003g0121 others(4): Show |
7 | HG00544.hp1 NA18747.hp2 NA18939.hp2 others(4): Show |
intron_variant | MODIFIER | c.27-28193C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148578455 | |||||||
chr5:148578466 | C | G | 1 | a0001c0001t0002g0082 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.27-28204G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148578466 | |||||||
chr5:148578479 | C | T | 3 | a0001c0001t0001g0181 a0001c0001t0002g0055 a0001c0001t0002g0062 |
3 | HG02738.hp2 NA18977.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.27-28217G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148578479 | |||||||
chr5:148578500 | T | G | 1 | a0001c0001t0006g0268 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.27-28238A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148578500 | |||||||
chr5:148578554 | C | T | 2 | a0001c0001t0001g0243 a0001c0001t0026g0184 |
2 | HG01884.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.27-28292G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148578554 | |||||||
chr5:148578589 | G | A | 1 | a0003c0009t0027g0307 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.27-28327C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148578589 | |||||||
chr5:148578595 | C | A | 63 | a0001c0001t0001g0179 a0001c0001t0001g0201 a0001c0001t0001g0204 others(60): Show |
64 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.27-28333G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148578595 | |||||||
chr5:148578700 | G | A | 195 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0171 others(192): Show |
197 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.27-28438C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148578700 | |||||||
chr5:148578976 | A | C | 1 | a0001c0001t0001g0280 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.27-28714T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148578976 | |||||||
chr5:148579001 | G | T | 2 | a0001c0001t0002g0081 a0001c0001t0002g0082 |
2 | NA18939.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.27-28739C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148579001 | |||||||
chr5:148579164 | C | T | 3 | a0001c0001t0001g0183 a0001c0001t0001g0195 a0001c0001t0001g0196 |
3 | HG02486.hp1 HG02970.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.27-28902G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148579164 | |||||||
chr5:148579219 | C | A | 1 | a0001c0001t0003g0087 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.27-28957G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148579219 | |||||||
chr5:148579221 | T | C | 2 | a0001c0001t0008g0134 a0001c0001t0008g0135 |
2 | NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.27-28959A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148579221 | |||||||
chr5:148579326 | G | A | 1 | a0001c0001t0003g0087 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.27-29064C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148579326 | |||||||
chr5:148579417 | T | C | 104 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0171 others(101): Show |
105 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.27-29155A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148579417 | |||||||
chr5:148579623 | T | C | 63 | a0001c0001t0001g0179 a0001c0001t0001g0201 a0001c0001t0001g0204 others(60): Show |
64 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.27-29361A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148579623 | |||||||
chr5:148579848 | C | T | 63 | a0001c0001t0001g0179 a0001c0001t0001g0201 a0001c0001t0001g0204 others(60): Show |
64 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.27-29586G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148579848 | |||||||
chr5:148579997 | G | A | 1 | a0001c0001t0003g0100 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.27-29735C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148579997 | |||||||
chr5:148579999 | G | C | 1 | a0001c0001t0003g0100 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.27-29737C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148579999 | |||||||
chr5:148580320 | G | A | 1 | a0001c0001t0002g0043 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.27-30058C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148580320 | |||||||
chr5:148580408 | T | C | 5 | a0001c0001t0003g0102 a0001c0001t0011g0103 a0001c0001t0011g0105 others(2): Show |
5 | HG01496.hp2 HG01884.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.27-30146A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148580408 | |||||||
chr5:148580448 | T | C | 9 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0251 others(6): Show |
9 | HG00140.hp1 HG01074.hp1 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.27-30186A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148580448 | |||||||
chr5:148580565 | A | G | 96 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0177 others(93): Show |
97 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.27-30303T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148580565 | |||||||
chr5:148580609 | C | T | 2 | a0001c0001t0008g0134 a0001c0001t0008g0135 |
2 | NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.27-30347G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148580609 | |||||||
chr5:148580613 | A | T | 96 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0177 others(93): Show |
97 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.27-30351T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148580613 | |||||||
chr5:148580650 | G | A | 1 | a0001c0001t0002g0010 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.27-30388C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148580650 | |||||||
chr5:148580784 | C | T | 6 | a0001c0001t0001g0198 a0001c0001t0003g0114 a0001c0001t0003g0115 others(3): Show |
6 | HG02257.hp1 HG02451.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.27-30522G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148580784 | |||||||
chr5:148580951 | TC | T | 9 | a0001c0001t0001g0209 a0001c0001t0002g0040 a0001c0001t0002g0053 others(6): Show |
9 | HG02132.hp1 NA18612.hp1 NA18747.hp1 others(6): Show |
intron_variant | MODIFIER | c.27-30690delG | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148580951 | |||||||
chr5:148581022 | CT | C | 194 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0171 others(191): Show |
196 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.27-30761delA | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148581022 | |||||||
chr5:148581074 | G | T | 2 | a0001c0001t0002g0031 a0001c0001t0003g0130 |
2 | NA18967.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.27-30812C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148581074 | |||||||
chr5:148581075 | T | G | 2 | a0001c0001t0002g0031 a0001c0001t0003g0130 |
2 | NA18967.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.27-30813A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148581075 | |||||||
chr5:148581245 | T | A | 1 | a0001c0001t0012g0220 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.27-30983A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148581245 | |||||||
chr5:148581394 | C | T | 4 | a0001c0001t0001g0173 a0001c0001t0001g0190 a0001c0001t0001g0191 others(1): Show |
4 | HG01891.hp1 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.27-31132G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148581394 | |||||||
chr5:148581432 | A | C | 5 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0190 others(2): Show |
6 | HG01891.hp1 HG02818.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.27-31170T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148581432 | |||||||
chr5:148581433 | GC | G | 95 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0177 others(92): Show |
96 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.27-31172delG | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148581433 | |||||||
chr5:148581439 | C | T | 95 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0177 others(92): Show |
96 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.27-31177G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148581439 | |||||||
chr5:148581529 | G | T | 1 | a0001c0001t0026g0184 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.27-31267C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148581529 | |||||||
chr5:148581573 | C | A | 7 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0231 others(4): Show |
7 | HG00597.hp1 HG00673.hp2 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.27-31311G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148581573 | |||||||
chr5:148581772 | G | A | 1 | a0003c0009t0027g0307 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.27-31510C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148581772 | |||||||
chr5:148581941 | C | G | 106 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0171 others(103): Show |
107 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.27-31679G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148581941 | |||||||
chr5:148582040 | C | T | 3 | a0001c0001t0001g0181 a0001c0001t0002g0055 a0001c0001t0002g0062 |
3 | HG02738.hp2 NA18977.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.27-31778G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148582040 | |||||||
chr5:148582069 | A | G | 1 | a0001c0001t0002g0037 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.27-31807T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148582069 | |||||||
chr5:148582164 | G | C | 1 | a0001c0001t0003g0087 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.27-31902C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148582164 | |||||||
chr5:148582314 | A | T | 1 | a0001c0001t0001g0192 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.27-32052T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148582314 | |||||||
chr5:148582396 | C | T | 96 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0177 others(93): Show |
97 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.27-32134G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148582396 | |||||||
chr5:148582710 | G | A | 14 | a0001c0001t0001g0185 a0001c0001t0001g0187 a0001c0001t0001g0188 others(11): Show |
14 | HG01069.hp2 HG01071.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.27-32448C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148582710 | |||||||
chr5:148582732 | C | G | 3 | a0001c0001t0001g0171 a0001c0001t0001g0248 a0001c0001t0001g0301 |
3 | HG00738.hp2 HG02698.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.27-32470G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148582732 | |||||||
chr5:148582775 | C | T | 1 | a0001c0001t0026g0184 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.27-32513G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148582775 | |||||||
chr5:148582844 | C | T | 114 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0177 others(111): Show |
115 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.27-32582G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148582844 | |||||||
chr5:148582970 | T | C | 1 | a0001c0001t0003g0087 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.27-32708A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148582970 | |||||||
chr5:148583104 | G | A | 17 | a0001c0001t0001g0183 a0001c0001t0001g0185 a0001c0001t0001g0187 others(14): Show |
17 | HG01069.hp2 HG01071.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.27-32842C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148583104 | |||||||
chr5:148583168 | C | T | 1 | a0001c0001t0003g0087 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.27-32906G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148583168 | |||||||
chr5:148583194 | A | G | 1 | a0001c0001t0005g0148 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.27-32932T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148583194 | |||||||
chr5:148583611 | C | CCAT | 60 | a0001c0001t0001g0163 a0001c0001t0001g0174 a0001c0001t0001g0180 others(57): Show |
60 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.27-33352_27-33350d others(5): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148583611 | |||||||
chr5:148583611 | C | CCATCAT | 4 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0003g0113 others(1): Show |
4 | HG01069.hp1 HG01496.hp1 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.27-33355_27-33350d others(8): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148583611 | |||||||
chr5:148583611 | CCAT | C | 34 | a0001c0001t0001g0183 a0001c0001t0001g0185 a0001c0001t0001g0186 others(31): Show |
34 | HG00673.hp1 HG01069.hp2 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.27-33352_27-33350d others(5): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148583611 | |||||||
chr5:148583611 | CCATCAT | C | 86 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0177 others(83): Show |
87 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.27-33355_27-33350d others(8): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148583611 | |||||||
chr5:148583651 | T | C | 1 | a0001c0001t0001g0238 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.27-33389A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148583651 | |||||||
chr5:148583684 | A | G | 182 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0177 others(179): Show |
184 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.27-33422T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148583684 | |||||||
chr5:148583860 | C | G | 117 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0177 others(114): Show |
118 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.27-33598G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148583860 | |||||||
chr5:148584110 | C | A | 1 | a0001c0001t0001g0248 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.27-33848G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148584110 | |||||||
chr5:148584821 | T | C | 1 | a0001c0001t0003g0087 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.27-34559A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148584821 | |||||||
chr5:148585034 | G | A | 1 | a0001c0001t0003g0087 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.27-34772C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148585034 | |||||||
chr5:148585095 | C | A | 112 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0177 others(109): Show |
113 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.27-34833G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148585095 | |||||||
chr5:148585610 | A | G | 118 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0177 others(115): Show |
119 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.27-35348T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148585610 | |||||||
chr5:148586107 | C | CT | 4 | a0001c0001t0001g0186 a0001c0001t0001g0287 a0001c0001t0003g0114 others(1): Show |
4 | HG01167.hp1 HG02886.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.27-35846dupA | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148586107 | |||||||
chr5:148586330 | T | C | 1 | a0003c0009t0027g0307 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.27-36068A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148586330 | |||||||
chr5:148586456 | A | G | 118 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0177 others(115): Show |
119 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.27-36194T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148586456 | |||||||
chr5:148586576 | G | A | 64 | a0001c0001t0001g0179 a0001c0001t0001g0201 a0001c0001t0001g0204 others(61): Show |
65 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.27-36314C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148586576 | |||||||
chr5:148586683 | C | T | 71 | a0001c0001t0001g0202 a0001c0001t0001g0211 a0001c0001t0001g0213 others(68): Show |
71 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.27-36421G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148586683 | |||||||
chr5:148586827 | G | A | 14 | a0001c0001t0001g0185 a0001c0001t0001g0187 a0001c0001t0001g0188 others(11): Show |
14 | HG01069.hp2 HG01071.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.27-36565C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148586827 | |||||||
chr5:148587111 | A | G | 191 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0171 others(188): Show |
193 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.27-36849T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148587111 | |||||||
chr5:148587213 | T | A | 3 | a0001c0001t0003g0087 a0001c0001t0003g0096 a0001c0001t0003g0097 |
3 | HG00673.hp1 NA18951.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.27-36951A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148587213 | |||||||
chr5:148587245 | A | T | 1 | a0001c0001t0002g0026 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.27-36983T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148587245 | |||||||
chr5:148587430 | A | T | 4 | a0001c0001t0001g0198 a0001c0001t0024g0154 a0001c0002t0001g0197 others(1): Show |
4 | HG02257.hp1 HG02451.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.27-37168T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148587430 | |||||||
chr5:148587467 | G | A | 1 | a0001c0001t0010g0086 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.27-37205C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148587467 | |||||||
chr5:148587694 | A | T | 12 | a0001c0001t0001g0202 a0001c0001t0001g0211 a0001c0001t0001g0213 others(9): Show |
12 | HG01243.hp2 HG02055.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.27-37432T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148587694 | |||||||
chr5:148587936 | A | C | 67 | a0001c0001t0001g0179 a0001c0001t0001g0201 a0001c0001t0001g0209 others(64): Show |
68 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.27-37674T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148587936 | |||||||
chr5:148588019 | C | T | 4 | a0001c0001t0002g0005 a0001c0001t0003g0124 a0001c0001t0003g0126 others(1): Show |
4 | NA18941.hp1 NA18971.hp1 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.27-37757G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148588019 | |||||||
chr5:148588134 | A | C | 1 | a0001c0001t0026g0184 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.27-37872T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148588134 | |||||||
chr5:148588183 | A | G | 59 | a0001c0001t0001g0161 a0001c0001t0001g0164 a0001c0001t0001g0171 others(56): Show |
60 | HG00609.hp2 HG00673.hp1 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.27-37921T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148588183 | |||||||
chr5:148588341 | T | C | 2 | a0001c0001t0001g0214 a0001c0001t0001g0215 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.27-38079A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148588341 | |||||||
chr5:148588527 | C | CT | 17 | a0001c0001t0001g0163 a0001c0001t0001g0180 a0001c0001t0001g0193 others(14): Show |
17 | HG02056.hp1 HG02135.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.27-38266dupA | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148588527 | |||||||
chr5:148588527 | CT | C | 115 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0164 others(112): Show |
118 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.27-38266delA | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148588527 | |||||||
chr5:148588527 | CTT | C | 7 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0002g0081 others(4): Show |
7 | HG02145.hp2 HG02965.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.27-38267_27-38266d others(4): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148588527 | |||||||
chr5:148588527 | CTTTTTTT others(5): Show |
C | 22 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0302 others(19): Show |
22 | HG01257.hp2 HG01952.hp1 HG02148.hp2 others(19): Show |
intron_variant | MODIFIER | c.27-38277_27-38266d others(14): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148588527 | |||||||
chr5:148588528 | T | C | 3 | a0001c0001t0001g0271 a0001c0001t0002g0032 a0001c0001t0002g0054 |
3 | HG03654.hp2 NA19067.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.27-38266A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148588528 | |||||||
chr5:148588529 | T | C | 61 | a0001c0001t0001g0179 a0001c0001t0001g0201 a0001c0001t0001g0209 others(58): Show |
62 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.27-38267A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148588529 | |||||||
chr5:148588530 | T | C | 2 | a0001c0001t0002g0081 a0001c0001t0003g0099 |
2 | NA18939.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.27-38268A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148588530 | |||||||
chr5:148588531 | T | C | 1 | a0001c0001t0002g0040 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.27-38269A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148588531 | |||||||
chr5:148588603 | C | T | 1 | a0001c0006t0003g0110 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.27-38341G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148588603 | |||||||
chr5:148588618 | G | A | 6 | a0001c0001t0003g0101 a0001c0001t0003g0102 a0001c0001t0011g0103 others(3): Show |
6 | HG01496.hp2 HG01884.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.27-38356C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148588618 | |||||||
chr5:148588679 | T | C | 2 | a0001c0001t0026g0184 a0001c0006t0003g0110 |
2 | HG01884.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.27-38417A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148588679 | |||||||
chr5:148588772 | C | T | 1 | a0001c0001t0001g0278 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.27-38510G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148588772 | |||||||
chr5:148588951 | G | A | 19 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0302 others(16): Show |
19 | HG01257.hp2 HG01952.hp1 HG02148.hp2 others(16): Show |
intron_variant | MODIFIER | c.27-38689C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148588951 | |||||||
chr5:148589034 | C | G | 22 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0302 others(19): Show |
22 | HG01257.hp2 HG01952.hp1 HG02148.hp2 others(19): Show |
intron_variant | MODIFIER | c.27-38772G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148589034 | |||||||
chr5:148589114 | T | C | 26 | a0001c0001t0001g0198 a0001c0001t0001g0243 a0001c0001t0001g0244 others(23): Show |
26 | HG01257.hp2 HG01952.hp1 HG02148.hp2 others(23): Show |
intron_variant | MODIFIER | c.27-38852A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148589114 | |||||||
chr5:148589147 | C | T | 1 | a0001c0001t0001g0294 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.27-38885G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148589147 | |||||||
chr5:148589179 | T | C | 20 | a0001c0001t0001g0161 a0001c0001t0001g0164 a0001c0001t0001g0171 others(17): Show |
21 | HG02145.hp2 HG02451.hp2 HG02572.hp2 others(18): Show |
intron_variant | MODIFIER | c.27-38917A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148589179 | |||||||
chr5:148589295 | G | A | 3 | a0001c0004t0003g0118 a0001c0005t0005g0146 a0001c0005t0005g0149 |
3 | HG02559.hp2 HG02735.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.27-39033C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148589295 | |||||||
chr5:148589370 | C | T | 1 | a0001c0001t0001g0185 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.27-39108G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148589370 | |||||||
chr5:148589378 | G | T | 5 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0190 others(2): Show |
6 | HG01891.hp1 HG02818.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.27-39116C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148589378 | |||||||
chr5:148589642 | T | C | 1 | a0001c0001t0003g0127 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.27-39380A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148589642 | |||||||
chr5:148589784 | C | T | 22 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0302 others(19): Show |
22 | HG01257.hp2 HG01952.hp1 HG02148.hp2 others(19): Show |
intron_variant | MODIFIER | c.27-39522G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148589784 | |||||||
chr5:148589793 | A | T | 15 | a0001c0001t0002g0020 a0001c0001t0002g0021 a0001c0001t0002g0022 others(12): Show |
15 | HG00609.hp2 HG00673.hp1 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.27-39531T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148589793 | |||||||
chr5:148589821 | C | T | 22 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0302 others(19): Show |
22 | HG01257.hp2 HG01952.hp1 HG02148.hp2 others(19): Show |
intron_variant | MODIFIER | c.27-39559G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148589821 | |||||||
chr5:148590029 | A | G | 1 | a0001c0004t0003g0118 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.27-39767T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148590029 | |||||||
chr5:148590287 | C | CT | 10 | a0001c0001t0001g0183 a0001c0001t0001g0279 a0001c0001t0001g0285 others(7): Show |
10 | HG00438.hp2 HG01884.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.27-40026dupA | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148590287 | |||||||
chr5:148590287 | CT | C | 167 | a0001c0001t0001g0003 a0001c0001t0001g0172 a0001c0001t0001g0173 others(164): Show |
168 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.27-40026delA | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148590287 | |||||||
chr5:148590287 | CTT | C | 31 | a0001c0001t0001g0161 a0001c0001t0001g0164 a0001c0001t0001g0176 others(28): Show |
32 | HG01433.hp1 HG02145.hp1 HG02145.hp2 others(29): Show |
intron_variant | MODIFIER | c.27-40027_27-40026d others(4): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148590287 | |||||||
chr5:148590287 | CTTT | C | 7 | a0001c0001t0001g0171 a0001c0001t0003g0091 a0001c0001t0008g0134 others(4): Show |
7 | HG02451.hp2 HG02698.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.27-40028_27-40026d others(5): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148590287 | |||||||
chr5:148590298 | T | C | 1 | a0001c0001t0003g0099 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.27-40036A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148590298 | |||||||
chr5:148590320 | C | CA | 6 | a0001c0001t0001g0193 a0001c0001t0001g0199 a0001c0001t0003g0090 others(3): Show |
6 | HG02258.hp1 HG03041.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.27-40059dupT | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148590320 | |||||||
chr5:148590338 | G | T | 15 | a0001c0001t0002g0020 a0001c0001t0002g0021 a0001c0001t0002g0022 others(12): Show |
15 | HG00609.hp2 HG00673.hp1 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.27-40076C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148590338 | |||||||
chr5:148590400 | G | GT | 59 | a0001c0001t0001g0161 a0001c0001t0001g0164 a0001c0001t0001g0171 others(56): Show |
60 | HG00609.hp2 HG00673.hp1 HG01257.hp2 others(57): Show |
intron_variant | MODIFIER | c.27-40139_27-40138i others(3): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148590400 | |||||||
chr5:148590484 | C | T | 1 | a0001c0001t0005g0144 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.27-40222G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148590484 | |||||||
chr5:148590538 | C | G | 2 | a0001c0002t0003g0088 a0003c0009t0027g0307 |
2 | HG01243.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.27-40276G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148590538 | |||||||
chr5:148590599 | T | C | 1 | a0001c0001t0001g0216 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.27-40337A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148590599 | |||||||
chr5:148590711 | G | A | 1 | a0001c0001t0026g0184 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.27-40449C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148590711 | |||||||
chr5:148590921 | C | T | 66 | a0001c0001t0001g0179 a0001c0001t0001g0201 a0001c0001t0001g0209 others(63): Show |
67 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.27-40659G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148590921 | |||||||
chr5:148590922 | G | A | 20 | a0001c0001t0001g0161 a0001c0001t0001g0164 a0001c0001t0001g0171 others(17): Show |
21 | HG02145.hp2 HG02451.hp2 HG02572.hp2 others(18): Show |
intron_variant | MODIFIER | c.27-40660C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148590922 | |||||||
chr5:148591069 | C | A | 1 | a0001c0001t0026g0184 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.27-40807G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148591069 | |||||||
chr5:148591193 | T | A | 1 | a0001c0001t0005g0139 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.27-40931A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148591193 | |||||||
chr5:148591277 | G | A | 1 | a0001c0001t0002g0013 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.27-41015C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148591277 | |||||||
chr5:148591308 | A | C | 4 | a0001c0001t0001g0183 a0001c0001t0001g0195 a0001c0001t0001g0196 others(1): Show |
4 | HG02055.hp2 HG02486.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.27-41046T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148591308 | |||||||
chr5:148591323 | T | A | 1 | a0001c0001t0001g0225 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.27-41061A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148591323 | |||||||
chr5:148591630 | A | G | 17 | a0001c0001t0002g0020 a0001c0001t0002g0021 a0001c0001t0002g0022 others(14): Show |
17 | HG00609.hp2 HG00673.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.27-41368T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148591630 | |||||||
chr5:148591873 | T | C | 21 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0183 others(18): Show |
22 | HG01069.hp2 HG01071.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.27-41611A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148591873 | |||||||
chr5:148592105 | G | A | 19 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0302 others(16): Show |
19 | HG01257.hp2 HG01952.hp1 HG02148.hp2 others(16): Show |
intron_variant | MODIFIER | c.27-41843C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148592105 | |||||||
chr5:148592113 | C | T | 1 | a0001c0001t0010g0086 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.27-41851G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148592113 | |||||||
chr5:148592135 | C | CA | 23 | a0001c0001t0001g0161 a0001c0001t0001g0164 a0001c0001t0001g0171 others(20): Show |
24 | HG02145.hp2 HG02451.hp2 HG02572.hp2 others(21): Show |
intron_variant | MODIFIER | c.27-41874dupT | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148592135 | |||||||
chr5:148592310 | T | A | 1 | a0001c0001t0008g0135 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.27-42048A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148592310 | |||||||
chr5:148592342 | G | T | 15 | a0001c0001t0002g0020 a0001c0001t0002g0021 a0001c0001t0002g0022 others(12): Show |
15 | HG00609.hp2 HG00673.hp1 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.27-42080C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148592342 | |||||||
chr5:148592403 | A | G | 5 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0190 others(2): Show |
6 | HG01891.hp1 HG02818.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.27-42141T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148592403 | |||||||
chr5:148592479 | G | GT | 17 | a0001c0001t0002g0020 a0001c0001t0002g0021 a0001c0001t0002g0022 others(14): Show |
17 | HG00609.hp2 HG00673.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.27-42218dupA | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148592479 | |||||||
chr5:148592543 | C | T | 42 | a0001c0001t0001g0161 a0001c0001t0001g0164 a0001c0001t0001g0171 others(39): Show |
43 | HG01257.hp2 HG01952.hp1 HG02145.hp2 others(40): Show |
intron_variant | MODIFIER | c.27-42281G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148592543 | |||||||
chr5:148592604 | T | C | 1 | a0001c0001t0003g0100 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.27-42342A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148592604 | |||||||
chr5:148592744 | G | T | 3 | a0001c0001t0001g0185 a0001c0001t0026g0184 a0001c0006t0003g0110 |
3 | HG01884.hp1 HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.27-42482C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148592744 | |||||||
chr5:148593056 | G | A | 9 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0009g0155 others(6): Show |
9 | HG02559.hp1 HG02559.hp2 HG02735.hp2 others(6): Show |
intron_variant | MODIFIER | c.27-42794C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148593056 | |||||||
chr5:148593249 | G | A | 19 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0302 others(16): Show |
19 | HG01257.hp2 HG01952.hp1 HG02148.hp2 others(16): Show |
intron_variant | MODIFIER | c.27-42987C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148593249 | |||||||
chr5:148593565 | A | G | 1 | a0001c0001t0002g0058 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.27-43303T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148593565 | |||||||
chr5:148593686 | C | T | 1 | a0001c0006t0003g0110 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.26+43303G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148593686 | |||||||
chr5:148593694 | G | C | 3 | a0001c0001t0008g0134 a0001c0001t0008g0135 a0001c0002t0008g0137 |
3 | HG02922.hp1 NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.26+43295C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148593694 | |||||||
chr5:148593702 | A | G | 19 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0302 others(16): Show |
19 | HG01257.hp2 HG01952.hp1 HG02148.hp2 others(16): Show |
intron_variant | MODIFIER | c.26+43287T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148593702 | |||||||
chr5:148593765 | A | G | 3 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0304 |
3 | HG02615.hp2 HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.26+43224T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148593765 | |||||||
chr5:148593806 | T | C | 1 | a0001c0001t0001g0176 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.26+43183A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148593806 | |||||||
chr5:148593837 | T | A | 1 | a0001c0001t0001g0192 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.26+43152A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148593837 | |||||||
chr5:148593882 | A | G | 5 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0190 others(2): Show |
6 | HG01891.hp1 HG02818.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.26+43107T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148593882 | |||||||
chr5:148594297 | A | G | 2 | a0001c0001t0001g0302 a0001c0001t0012g0205 |
2 | HG02647.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.26+42692T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148594297 | |||||||
chr5:148594346 | G | A | 1 | a0001c0001t0003g0090 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.26+42643C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148594346 | |||||||
chr5:148594351 | C | CGT | 32 | a0001c0001t0001g0164 a0001c0001t0001g0181 a0001c0001t0001g0251 others(29): Show |
32 | HG00609.hp2 HG00673.hp1 HG00673.hp2 others(29): Show |
intron_variant | MODIFIER | c.26+42636_26+42637d others(4): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148594351 | |||||||
chr5:148594351 | C | CGTGT | 22 | a0001c0001t0001g0198 a0001c0001t0001g0243 a0001c0001t0001g0244 others(19): Show |
22 | HG01257.hp2 HG01952.hp1 HG02148.hp2 others(19): Show |
intron_variant | MODIFIER | c.26+42634_26+42637d others(6): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148594351 | |||||||
chr5:148594351 | CGT | C | 11 | a0001c0001t0001g0178 a0001c0001t0001g0193 a0001c0001t0001g0199 others(8): Show |
11 | HG01433.hp1 HG01884.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.26+42636_26+42637d others(4): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148594351 | |||||||
chr5:148594351 | CGTGT | C | 87 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0179 others(84): Show |
89 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.26+42634_26+42637d others(6): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148594351 | |||||||
chr5:148594387 | C | A | 1 | a0001c0001t0003g0113 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.26+42602G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148594387 | |||||||
chr5:148594576 | A | C | 21 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0302 others(18): Show |
21 | HG00423.hp2 HG00544.hp2 HG01257.hp2 others(18): Show |
intron_variant | MODIFIER | c.26+42413T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148594576 | |||||||
chr5:148594690 | G | A | 1 | a0001c0001t0003g0100 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.26+42299C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148594690 | |||||||
chr5:148594779 | T | C | 1 | a0001c0001t0001g0245 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.26+42210A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148594779 | |||||||
chr5:148594818 | A | G | 1 | a0001c0001t0005g0138 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.26+42171T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148594818 | |||||||
chr5:148595081 | G | GT | 19 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0302 others(16): Show |
19 | HG01257.hp2 HG01952.hp1 HG02148.hp2 others(16): Show |
intron_variant | MODIFIER | c.26+41907dupA | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148595081 | |||||||
chr5:148595082 | T | G | 15 | a0001c0001t0002g0020 a0001c0001t0002g0021 a0001c0001t0002g0022 others(12): Show |
15 | HG00609.hp2 HG00673.hp1 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.26+41907A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148595082 | |||||||
chr5:148595310 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.26+41679G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148595310 | |||||||
chr5:148595450 | C | T | 15 | a0001c0001t0002g0020 a0001c0001t0002g0021 a0001c0001t0002g0022 others(12): Show |
15 | HG00609.hp2 HG00673.hp1 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.26+41539G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148595450 | |||||||
chr5:148595548 | CA | C | 3 | a0001c0001t0008g0134 a0001c0001t0008g0135 a0001c0002t0008g0137 |
3 | HG02922.hp1 NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.26+41440delT | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148595548 | |||||||
chr5:148595670 | T | C | 2 | a0001c0001t0001g0225 a0001c0004t0001g0242 |
2 | HG02300.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.26+41319A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148595670 | |||||||
chr5:148595808 | A | C | 1 | a0001c0001t0003g0112 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.26+41181T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148595808 | |||||||
chr5:148595954 | A | G | 3 | a0001c0001t0001g0277 a0001c0001t0004g0276 a0001c0001t0006g0268 |
3 | NA18991.hp2 NA19011.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.26+41035T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148595954 | |||||||
chr5:148596018 | T | C | 1 | a0001c0001t0002g0066 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.26+40971A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148596018 | |||||||
chr5:148596401 | T | C | 1 | a0001c0001t0002g0008 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.26+40588A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148596401 | |||||||
chr5:148596481 | C | T | 5 | a0001c0001t0001g0198 a0001c0001t0010g0086 a0001c0001t0024g0154 others(2): Show |
5 | HG02257.hp1 HG02451.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.26+40508G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148596481 | |||||||
chr5:148596638 | C | A | 1 | a0001c0001t0002g0058 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.26+40351G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148596638 | |||||||
chr5:148596656 | A | G | 1 | a0001c0001t0001g0283 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.26+40333T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148596656 | |||||||
chr5:148596783 | CATCTTTC others(13): Show |
C | 1 | a0001c0001t0001g0178 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.26+40186_26+40205d others(22): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148596783 | |||||||
chr5:148596850 | T | A | 1 | a0001c0001t0002g0075 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.26+40139A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148596850 | |||||||
chr5:148596927 | A | G | 2 | a0001c0001t0026g0184 a0001c0006t0003g0110 |
2 | HG01884.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.26+40062T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148596927 | |||||||
chr5:148597221 | A | G | 1 | a0001c0001t0001g0198 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.26+39768T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148597221 | |||||||
chr5:148597696 | A | G | 1 | a0001c0001t0002g0056 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.26+39293T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148597696 | |||||||
chr5:148597700 | C | A | 6 | a0001c0001t0001g0294 a0001c0001t0001g0295 a0001c0001t0004g0293 others(3): Show |
6 | HG00544.hp1 NA18939.hp2 NA18957.hp2 others(3): Show |
intron_variant | MODIFIER | c.26+39289G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148597700 | |||||||
chr5:148597860 | C | A | 4 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 others(1): Show |
4 | HG00099.hp2 HG00323.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.26+39129G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148597860 | |||||||
chr5:148598041 | T | C | 1 | a0001c0001t0026g0184 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.26+38948A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148598041 | |||||||
chr5:148598056 | G | T | 1 | a0001c0001t0002g0060 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.26+38933C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148598056 | |||||||
chr5:148598057 | T | C | 21 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0302 others(18): Show |
21 | HG00423.hp2 HG00544.hp2 HG01257.hp2 others(18): Show |
intron_variant | MODIFIER | c.26+38932A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148598057 | |||||||
chr5:148598172 | G | A | 1 | a0001c0001t0011g0103 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.26+38817C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148598172 | |||||||
chr5:148598252 | C | T | 1 | a0001c0001t0001g0245 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.26+38737G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148598252 | |||||||
chr5:148598409 | A | G | 39 | a0001c0001t0001g0161 a0001c0001t0001g0164 a0001c0001t0001g0171 others(36): Show |
40 | HG01257.hp2 HG01952.hp1 HG02145.hp2 others(37): Show |
intron_variant | MODIFIER | c.26+38580T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148598409 | |||||||
chr5:148598525 | C | A | 1 | a0001c0001t0001g0279 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.26+38464G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148598525 | |||||||
chr5:148598558 | A | G | 1 | a0001c0001t0001g0245 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.26+38431T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148598558 | |||||||
chr5:148598632 | C | T | 2 | a0001c0001t0010g0083 a0001c0001t0010g0084 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.26+38357G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148598632 | |||||||
chr5:148598690 | A | T | 66 | a0001c0001t0001g0179 a0001c0001t0001g0201 a0001c0001t0001g0209 others(63): Show |
67 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.26+38299T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148598690 | |||||||
chr5:148598829 | G | A | 1 | a0001c0005t0005g0146 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.26+38160C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148598829 | |||||||
chr5:148598839 | T | C | 1 | a0001c0001t0005g0151 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.26+38150A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148598839 | |||||||
chr5:148598895 | C | T | 1 | a0001c0001t0001g0280 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.26+38094G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148598895 | |||||||
chr5:148599139 | C | T | 2 | a0001c0001t0010g0083 a0001c0001t0010g0084 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.26+37850G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148599139 | |||||||
chr5:148599415 | C | T | 66 | a0001c0001t0001g0179 a0001c0001t0001g0201 a0001c0001t0001g0209 others(63): Show |
67 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.26+37574G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148599415 | |||||||
chr5:148599790 | T | C | 1 | a0001c0001t0004g0169 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.26+37199A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148599790 | |||||||
chr5:148599803 | A | G | 1 | a0001c0001t0026g0184 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.26+37186T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148599803 | |||||||
chr5:148599989 | C | T | 1 | a0001c0001t0006g0240 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.26+37000G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148599989 | |||||||
chr5:148600091 | T | C | 16 | a0001c0001t0002g0020 a0001c0001t0002g0021 a0001c0001t0002g0022 others(13): Show |
16 | HG00609.hp2 HG00673.hp1 HG01928.hp2 others(13): Show |
intron_variant | MODIFIER | c.26+36898A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148600091 | |||||||
chr5:148600249 | A | G | 1 | a0001c0001t0026g0184 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.26+36740T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148600249 | |||||||
chr5:148600348 | TA | T | 13 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0183 others(10): Show |
14 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.26+36640delT | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148600348 | |||||||
chr5:148600349 | A | T | 11 | a0001c0001t0001g0193 a0001c0001t0001g0199 a0001c0001t0001g0251 others(8): Show |
11 | HG01884.hp1 HG02258.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.26+36640T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148600349 | |||||||
chr5:148600349 | AT | A | 77 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0185 others(74): Show |
78 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.26+36639delA | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148600349 | |||||||
chr5:148600351 | T | A | 48 | a0001c0001t0001g0161 a0001c0001t0001g0164 a0001c0001t0001g0171 others(45): Show |
49 | HG00609.hp2 HG00673.hp1 HG01243.hp2 others(46): Show |
intron_variant | MODIFIER | c.26+36638A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148600351 | |||||||
chr5:148600415 | C | T | 1 | a0001c0001t0001g0245 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.26+36574G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148600415 | |||||||
chr5:148600434 | T | C | 1 | a0001c0001t0003g0100 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.26+36555A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148600434 | |||||||
chr5:148600474 | T | C | 19 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0302 others(16): Show |
19 | HG01257.hp2 HG01952.hp1 HG02148.hp2 others(16): Show |
intron_variant | MODIFIER | c.26+36515A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148600474 | |||||||
chr5:148600493 | A | C | 1 | a0001c0001t0004g0255 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.26+36496T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148600493 | |||||||
chr5:148600521 | T | A | 16 | a0001c0001t0002g0020 a0001c0001t0002g0021 a0001c0001t0002g0022 others(13): Show |
16 | HG00609.hp2 HG00673.hp1 HG01928.hp2 others(13): Show |
intron_variant | MODIFIER | c.26+36468A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148600521 | |||||||
chr5:148600739 | A | T | 1 | a0001c0001t0003g0115 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.26+36250T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148600739 | |||||||
chr5:148600762 | A | G | 3 | a0001c0001t0008g0134 a0001c0001t0008g0135 a0001c0002t0008g0137 |
3 | HG02922.hp1 NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.26+36227T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148600762 | |||||||
chr5:148600932 | C | T | 16 | a0001c0001t0002g0020 a0001c0001t0002g0021 a0001c0001t0002g0022 others(13): Show |
16 | HG00609.hp2 HG00673.hp1 HG01928.hp2 others(13): Show |
intron_variant | MODIFIER | c.26+36057G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148600932 | |||||||
chr5:148600976 | C | CA | 114 | a0001c0001t0001g0163 a0001c0001t0001g0174 a0001c0001t0001g0177 others(111): Show |
114 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.26+36012dupT | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148600976 | |||||||
chr5:148600976 | C | CAA | 58 | a0001c0001t0001g0003 a0001c0001t0001g0180 a0001c0001t0001g0181 others(55): Show |
59 | HG00140.hp1 HG00544.hp1 HG00673.hp2 others(56): Show |
intron_variant | MODIFIER | c.26+36011_26+36012d others(4): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148600976 | |||||||
chr5:148600976 | C | CAAA | 10 | a0001c0001t0001g0173 a0001c0001t0001g0191 a0001c0001t0001g0211 others(7): Show |
10 | HG00438.hp1 HG00621.hp2 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.26+36010_26+36012d others(5): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148600976 | |||||||
chr5:148600976 | CA | C | 65 | a0001c0001t0001g0164 a0001c0001t0001g0172 a0001c0001t0001g0176 others(62): Show |
67 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.26+36012delT | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148600976 | |||||||
chr5:148600976 | CAAAAAAA others(2): Show |
C | 16 | a0001c0001t0002g0020 a0001c0001t0002g0021 a0001c0001t0002g0022 others(13): Show |
16 | HG00609.hp2 HG00673.hp1 HG01928.hp2 others(13): Show |
intron_variant | MODIFIER | c.26+36004_26+36012d others(11): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148600976 | |||||||
chr5:148601080 | G | C | 1 | a0001c0001t0001g0187 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.26+35909C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148601080 | |||||||
chr5:148601399 | G | A | 19 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0302 others(16): Show |
19 | HG01257.hp2 HG01952.hp1 HG02148.hp2 others(16): Show |
intron_variant | MODIFIER | c.26+35590C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148601399 | |||||||
chr5:148601604 | C | A | 1 | a0001c0001t0001g0280 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.26+35385G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148601604 | |||||||
chr5:148601626 | C | G | 20 | a0001c0001t0001g0161 a0001c0001t0001g0164 a0001c0001t0001g0171 others(17): Show |
21 | HG02145.hp2 HG02451.hp2 HG02572.hp2 others(18): Show |
intron_variant | MODIFIER | c.26+35363G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148601626 | |||||||
chr5:148601626 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.26+35363G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148601626 | |||||||
chr5:148602048 | A | G | 1 | a0001c0001t0001g0192 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.26+34941T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148602048 | |||||||
chr5:148602110 | G | C | 20 | a0001c0001t0001g0161 a0001c0001t0001g0164 a0001c0001t0001g0171 others(17): Show |
21 | HG02145.hp2 HG02451.hp2 HG02572.hp2 others(18): Show |
intron_variant | MODIFIER | c.26+34879C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148602110 | |||||||
chr5:148602760 | T | C | 1 | a0001c0001t0001g0238 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.26+34229A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148602760 | |||||||
chr5:148603114 | G | T | 3 | a0001c0001t0008g0134 a0001c0001t0008g0135 a0001c0002t0008g0137 |
3 | HG02922.hp1 NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.26+33875C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148603114 | |||||||
chr5:148603292 | C | T | 148 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0164 others(145): Show |
151 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.26+33697G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148603292 | |||||||
chr5:148603439 | G | A | 19 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0302 others(16): Show |
19 | HG01257.hp2 HG01952.hp1 HG02148.hp2 others(16): Show |
intron_variant | MODIFIER | c.26+33550C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148603439 | |||||||
chr5:148603472 | T | C | 1 | a0001c0001t0001g0182 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.26+33517A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148603472 | |||||||
chr5:148603670 | A | G | 2 | a0001c0001t0010g0083 a0001c0001t0010g0084 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.26+33319T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148603670 | |||||||
chr5:148603788 | G | T | 67 | a0001c0001t0001g0179 a0001c0001t0001g0201 a0001c0001t0001g0209 others(64): Show |
68 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.26+33201C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148603788 | |||||||
chr5:148603974 | T | C | 1 | a0001c0001t0001g0260 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.26+33015A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148603974 | |||||||
chr5:148604034 | A | G | 1 | a0001c0001t0002g0040 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.26+32955T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148604034 | |||||||
chr5:148604086 | T | C | 1 | a0001c0001t0001g0003 | 2 | HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.26+32903A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148604086 | |||||||
chr5:148604398 | A | G | 1 | a0001c0001t0005g0148 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.26+32591T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148604398 | |||||||
chr5:148604574 | G | T | 39 | a0001c0001t0001g0161 a0001c0001t0001g0164 a0001c0001t0001g0171 others(36): Show |
40 | HG01257.hp2 HG01952.hp1 HG02145.hp2 others(37): Show |
intron_variant | MODIFIER | c.26+32415C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148604574 | |||||||
chr5:148604717 | G | A | 3 | a0001c0001t0001g0163 a0001c0001t0001g0174 a0001c0001t0001g0180 |
3 | NA18994.hp1 NA19083.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.26+32272C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148604717 | |||||||
chr5:148605119 | G | A | 1 | a0001c0006t0003g0110 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.26+31870C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148605119 | |||||||
chr5:148605252 | TTTTC | T | 75 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0177 others(72): Show |
76 | HG00609.hp1 HG00609.hp2 HG00673.hp1 others(73): Show |
intron_variant | MODIFIER | c.26+31733_26+31736d others(6): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148605252 | |||||||
chr5:148605253 | TTTC | T | 58 | a0001c0001t0001g0179 a0001c0001t0001g0201 a0001c0001t0001g0209 others(55): Show |
59 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.26+31733_26+31735d others(5): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148605253 | |||||||
chr5:148605254 | TTC | T | 7 | a0001c0001t0001g0249 a0001c0001t0001g0253 a0001c0001t0001g0278 others(4): Show |
7 | HG00597.hp2 HG02027.hp2 NA18949.hp1 others(4): Show |
intron_variant | MODIFIER | c.26+31733_26+31734d others(4): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148605254 | |||||||
chr5:148605256 | CTTTT | C | 20 | a0001c0001t0001g0161 a0001c0001t0001g0164 a0001c0001t0001g0171 others(17): Show |
21 | HG02145.hp2 HG02451.hp2 HG02572.hp2 others(18): Show |
intron_variant | MODIFIER | c.26+31729_26+31732d others(6): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148605256 | |||||||
chr5:148605298 | G | A | 4 | a0001c0001t0001g0198 a0001c0001t0024g0154 a0001c0002t0001g0197 others(1): Show |
4 | HG02257.hp1 HG02451.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.26+31691C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148605298 | |||||||
chr5:148605320 | G | A | 16 | a0001c0001t0002g0020 a0001c0001t0002g0021 a0001c0001t0002g0022 others(13): Show |
16 | HG00609.hp2 HG00673.hp1 HG01928.hp2 others(13): Show |
intron_variant | MODIFIER | c.26+31669C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148605320 | |||||||
chr5:148605345 | G | A | 2 | a0001c0001t0001g0214 a0001c0001t0001g0215 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.26+31644C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148605345 | |||||||
chr5:148605473 | G | A | 2 | a0001c0005t0005g0146 a0001c0005t0005g0149 |
2 | HG02559.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.26+31516C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148605473 | |||||||
chr5:148605652 | C | T | 1 | a0001c0001t0002g0056 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.26+31337G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148605652 | |||||||
chr5:148605735 | G | A | 6 | a0001c0001t0001g0193 a0001c0001t0001g0199 a0001c0001t0003g0090 others(3): Show |
6 | HG02258.hp1 HG03041.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.26+31254C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148605735 | |||||||
chr5:148605747 | TA | T | 10 | a0001c0001t0001g0193 a0001c0001t0001g0199 a0001c0001t0001g0290 others(7): Show |
10 | HG01167.hp2 HG01884.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.26+31241delT | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148605747 | |||||||
chr5:148605925 | C | T | 20 | a0001c0001t0001g0161 a0001c0001t0001g0164 a0001c0001t0001g0171 others(17): Show |
21 | HG02145.hp2 HG02451.hp2 HG02572.hp2 others(18): Show |
intron_variant | MODIFIER | c.26+31064G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148605925 | |||||||
chr5:148606062 | A | C | 98 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0193 others(95): Show |
98 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.26+30927T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148606062 | |||||||
chr5:148606406 | T | C | 1 | a0001c0001t0004g0298 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.26+30583A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148606406 | |||||||
chr5:148606454 | A | G | 9 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(6): Show |
9 | HG01069.hp2 HG01071.hp2 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.26+30535T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148606454 | |||||||
chr5:148606458 | A | T | 3 | a0001c0004t0003g0118 a0001c0005t0005g0146 a0001c0005t0005g0149 |
3 | HG02559.hp2 HG02735.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.26+30531T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148606458 | |||||||
chr5:148606725 | C | T | 1 | a0001c0001t0001g0302 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.26+30264G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148606725 | |||||||
chr5:148606729 | T | C | 1 | a0003c0009t0027g0307 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.26+30260A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148606729 | |||||||
chr5:148607252 | C | T | 1 | a0001c0001t0005g0139 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.26+29737G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148607252 | |||||||
chr5:148607360 | T | C | 1 | a0001c0001t0003g0117 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.26+29629A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148607360 | |||||||
chr5:148607439 | C | T | 2 | a0001c0001t0001g0281 a0001c0001t0001g0283 |
2 | HG03239.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.26+29550G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148607439 | |||||||
chr5:148607539 | C | A | 1 | a0001c0001t0010g0086 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.26+29450G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148607539 | |||||||
chr5:148607550 | T | C | 5 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0199 others(2): Show |
5 | HG01361.hp2 HG01433.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.26+29439A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148607550 | |||||||
chr5:148607615 | G | C | 69 | a0001c0001t0001g0204 a0001c0001t0001g0250 a0001c0001t0001g0284 others(66): Show |
69 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.26+29374C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148607615 | |||||||
chr5:148607659 | T | C | 1 | a0001c0001t0002g0064 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.26+29330A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148607659 | |||||||
chr5:148607741 | T | C | 8 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(5): Show |
8 | HG01167.hp1 HG01884.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.26+29248A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148607741 | |||||||
chr5:148607824 | A | T | 1 | a0001c0001t0001g0251 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.26+29165T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148607824 | |||||||
chr5:148607988 | C | T | 1 | a0001c0001t0003g0100 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.26+29001G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148607988 | |||||||
chr5:148607989 | G | A | 1 | a0001c0001t0018g0104 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.26+29000C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148607989 | |||||||
chr5:148608166 | C | A | 2 | a0001c0001t0003g0095 a0001c0002t0003g0094 |
2 | HG02717.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.26+28823G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148608166 | |||||||
chr5:148608167 | C | T | 1 | a0001c0001t0006g0229 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.26+28822G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148608167 | |||||||
chr5:148608236 | T | A | 12 | a0001c0001t0002g0020 a0001c0001t0002g0021 a0001c0001t0002g0022 others(9): Show |
12 | HG00609.hp2 HG01928.hp2 HG01952.hp2 others(9): Show |
intron_variant | MODIFIER | c.26+28753A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148608236 | |||||||
chr5:148608303 | A | G | 20 | a0001c0001t0001g0161 a0001c0001t0001g0164 a0001c0001t0001g0171 others(17): Show |
21 | HG02056.hp2 HG02145.hp2 HG02451.hp2 others(18): Show |
intron_variant | MODIFIER | c.26+28686T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148608303 | |||||||
chr5:148608349 | G | A | 16 | a0001c0001t0001g0172 a0001c0001t0002g0020 a0001c0001t0002g0021 others(13): Show |
16 | HG00609.hp2 HG00673.hp1 HG01928.hp2 others(13): Show |
intron_variant | MODIFIER | c.26+28640C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148608349 | |||||||
chr5:148608365 | G | A | 1 | a0001c0001t0007g0065 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.26+28624C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148608365 | |||||||
chr5:148608414 | C | T | 78 | a0001c0001t0001g0204 a0001c0001t0001g0250 a0001c0001t0001g0251 others(75): Show |
78 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.26+28575G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148608414 | |||||||
chr5:148608420 | C | A | 4 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0199 others(1): Show |
4 | HG01361.hp2 HG01433.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.26+28569G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148608420 | |||||||
chr5:148608541 | A | G | 2 | a0001c0001t0012g0205 a0001c0001t0024g0154 |
2 | HG02451.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.26+28448T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148608541 | |||||||
chr5:148608588 | GT | G | 4 | a0001c0001t0001g0183 a0001c0001t0001g0195 a0001c0001t0001g0196 others(1): Show |
4 | HG02055.hp2 HG02486.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.26+28400delA | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148608588 | |||||||
chr5:148608876 | G | T | 1 | a0001c0001t0002g0052 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.26+28113C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148608876 | |||||||
chr5:148609115 | G | A | 101 | a0001c0001t0001g0161 a0001c0001t0001g0164 a0001c0001t0001g0171 others(98): Show |
103 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.26+27874C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148609115 | |||||||
chr5:148609247 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.26+27742G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148609247 | |||||||
chr5:148609285 | C | T | 72 | a0001c0001t0001g0172 a0001c0001t0001g0209 a0001c0001t0001g0249 others(69): Show |
73 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.26+27704G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148609285 | |||||||
chr5:148609581 | G | GT | 72 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0164 others(69): Show |
74 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.26+27407dupA | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148609581 | |||||||
chr5:148609581 | G | GTT | 16 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(13): Show |
16 | HG00738.hp1 HG01167.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.26+27406_26+27407d others(4): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148609581 | |||||||
chr5:148609581 | GT | G | 59 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0252 others(56): Show |
59 | HG00140.hp2 HG00408.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.26+27407delA | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148609581 | |||||||
chr5:148609602 | T | C | 68 | a0001c0001t0001g0204 a0001c0001t0001g0250 a0001c0001t0001g0251 others(65): Show |
68 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.26+27387A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148609602 | |||||||
chr5:148609817 | C | A | 1 | a0001c0002t0003g0088 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.26+27172G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148609817 | |||||||
chr5:148609818 | A | G | 26 | a0001c0001t0001g0161 a0001c0001t0001g0164 a0001c0001t0001g0171 others(23): Show |
27 | HG01167.hp1 HG01884.hp1 HG02056.hp2 others(24): Show |
intron_variant | MODIFIER | c.26+27171T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148609818 | |||||||
chr5:148609827 | A | T | 1 | a0001c0001t0003g0116 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.26+27162T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148609827 | |||||||
chr5:148609936 | AC | A | 74 | a0001c0001t0001g0172 a0001c0001t0001g0209 a0001c0001t0001g0249 others(71): Show |
75 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.26+27052delG | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148609936 | |||||||
chr5:148609951 | T | G | 1 | a0001c0001t0001g0222 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.26+27038A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148609951 | |||||||
chr5:148609966 | A | C | 54 | a0001c0001t0001g0209 a0001c0001t0001g0249 a0001c0001t0001g0253 others(51): Show |
55 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.26+27023T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148609966 | |||||||
chr5:148609979 | A | C | 26 | a0001c0001t0001g0161 a0001c0001t0001g0164 a0001c0001t0001g0171 others(23): Show |
27 | HG01167.hp1 HG01884.hp1 HG02056.hp2 others(24): Show |
intron_variant | MODIFIER | c.26+27010T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148609979 | |||||||
chr5:148610154 | C | T | 54 | a0001c0001t0001g0209 a0001c0001t0001g0249 a0001c0001t0001g0253 others(51): Show |
55 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.26+26835G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148610154 | |||||||
chr5:148610261 | C | G | 180 | a0001c0001t0001g0161 a0001c0001t0001g0164 a0001c0001t0001g0171 others(177): Show |
182 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.26+26728G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148610261 | |||||||
chr5:148610290 | G | T | 1 | a0001c0002t0003g0088 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.26+26699C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148610290 | |||||||
chr5:148610315 | C | T | 1 | a0001c0002t0003g0088 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.26+26674G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148610315 | |||||||
chr5:148610316 | G | A | 2 | a0001c0006t0003g0110 a0002c0003t0022g0109 |
2 | HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.26+26673C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148610316 | |||||||
chr5:148610320 | C | T | 1 | a0001c0001t0024g0154 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.26+26669G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148610320 | |||||||
chr5:148610375 | C | T | 7 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(4): Show |
7 | HG01167.hp1 HG01884.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.26+26614G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148610375 | |||||||
chr5:148610378 | C | G | 72 | a0001c0001t0001g0172 a0001c0001t0001g0209 a0001c0001t0001g0249 others(69): Show |
73 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.26+26611G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148610378 | |||||||
chr5:148610390 | C | A | 1 | a0001c0006t0003g0110 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.26+26599G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148610390 | |||||||
chr5:148610392 | G | A | 1 | a0001c0001t0002g0010 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.26+26597C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148610392 | |||||||
chr5:148610469 | G | C | 4 | a0001c0001t0008g0134 a0001c0001t0008g0135 a0001c0002t0008g0136 others(1): Show |
4 | HG02922.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.26+26520C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148610469 | |||||||
chr5:148610474 | C | T | 4 | a0001c0001t0008g0134 a0001c0001t0008g0135 a0001c0002t0008g0136 others(1): Show |
4 | HG02922.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.26+26515G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148610474 | |||||||
chr5:148610477 | C | G | 4 | a0001c0001t0008g0134 a0001c0001t0008g0135 a0001c0002t0008g0136 others(1): Show |
4 | HG02922.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.26+26512G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148610477 | |||||||
chr5:148610650 | A | G | 5 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0190 others(2): Show |
6 | HG01891.hp1 HG02818.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.26+26339T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148610650 | |||||||
chr5:148610689 | T | C | 219 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0164 others(216): Show |
222 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.26+26300A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148610689 | |||||||
chr5:148610699 | G | T | 54 | a0001c0001t0001g0209 a0001c0001t0001g0249 a0001c0001t0001g0253 others(51): Show |
55 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.26+26290C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148610699 | |||||||
chr5:148610714 | C | T | 1 | a0001c0001t0001g0281 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.26+26275G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148610714 | |||||||
chr5:148610751 | C | T | 1 | a0001c0001t0002g0046 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.26+26238G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148610751 | |||||||
chr5:148610825 | T | C | 1 | a0001c0002t0003g0088 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.26+26164A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148610825 | |||||||
chr5:148610870 | T | C | 204 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0164 others(201): Show |
207 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.26+26119A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148610870 | |||||||
chr5:148610871 | G | A | 3 | a0001c0001t0003g0132 a0001c0001t0003g0133 a0001c0001t0005g0001 |
4 | HG01071.hp1 HG01074.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.26+26118C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148610871 | |||||||
chr5:148610902 | C | T | 8 | a0001c0001t0001g0164 a0001c0001t0004g0002 a0001c0001t0004g0165 others(5): Show |
9 | NA18947.hp2 NA18962.hp1 NA18963.hp1 others(6): Show |
intron_variant | MODIFIER | c.26+26087G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148610902 | |||||||
chr5:148610912 | G | A | 2 | a0001c0001t0001g0177 a0001c0001t0001g0178 |
2 | HG01361.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.26+26077C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148610912 | |||||||
chr5:148610921 | G | C | 2 | a0001c0006t0003g0110 a0002c0003t0022g0109 |
2 | HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.26+26068C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148610921 | |||||||
chr5:148610962 | A | G | 1 | a0001c0001t0001g0216 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.26+26027T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148610962 | |||||||
chr5:148610998 | G | A | 1 | a0001c0001t0001g0208 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.26+25991C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148610998 | |||||||
chr5:148611023 | T | C | 2 | a0001c0006t0003g0110 a0002c0003t0022g0109 |
2 | HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.26+25966A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148611023 | |||||||
chr5:148611047 | C | T | 1 | a0001c0002t0003g0088 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.26+25942G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148611047 | |||||||
chr5:148611054 | G | C | 4 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0003g0114 others(1): Show |
4 | HG01361.hp2 HG01433.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.26+25935C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148611054 | |||||||
chr5:148611132 | A | G | 1 | a0001c0001t0002g0046 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.26+25857T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148611132 | |||||||
chr5:148611227 | A | G | 1 | a0001c0001t0001g0193 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.26+25762T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148611227 | |||||||
chr5:148611284 | C | T | 26 | a0001c0001t0001g0161 a0001c0001t0001g0164 a0001c0001t0001g0171 others(23): Show |
27 | HG01167.hp1 HG01884.hp1 HG02056.hp2 others(24): Show |
intron_variant | MODIFIER | c.26+25705G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148611284 | |||||||
chr5:148611321 | C | T | 2 | a0001c0001t0010g0086 a0001c0001t0024g0154 |
2 | HG02451.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.26+25668G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148611321 | |||||||
chr5:148611448 | A | G | 26 | a0001c0001t0001g0161 a0001c0001t0001g0164 a0001c0001t0001g0171 others(23): Show |
27 | HG01167.hp1 HG01884.hp1 HG02056.hp2 others(24): Show |
intron_variant | MODIFIER | c.26+25541T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148611448 | |||||||
chr5:148611539 | T | G | 180 | a0001c0001t0001g0161 a0001c0001t0001g0164 a0001c0001t0001g0171 others(177): Show |
182 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.26+25450A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148611539 | |||||||
chr5:148611594 | C | T | 76 | a0001c0001t0001g0204 a0001c0001t0001g0250 a0001c0001t0001g0251 others(73): Show |
76 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.26+25395G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148611594 | |||||||
chr5:148611635 | C | T | 4 | a0001c0001t0008g0134 a0001c0001t0008g0135 a0001c0002t0008g0136 others(1): Show |
4 | HG02922.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.26+25354G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148611635 | |||||||
chr5:148611677 | C | A | 1 | a0001c0001t0007g0065 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.26+25312G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148611677 | |||||||
chr5:148611722 | C | T | 67 | a0001c0001t0001g0204 a0001c0001t0001g0250 a0001c0001t0001g0284 others(64): Show |
67 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.26+25267G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148611722 | |||||||
chr5:148611740 | G | A | 1 | a0001c0001t0002g0017 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.26+25249C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148611740 | |||||||
chr5:148611766 | C | T | 2 | a0001c0001t0001g0226 a0001c0001t0001g0227 |
2 | NA18612.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.26+25223G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148611766 | |||||||
chr5:148611943 | A | C | 5 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0190 others(2): Show |
6 | HG01891.hp1 HG02818.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.26+25046T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148611943 | |||||||
chr5:148612020 | T | C | 18 | a0001c0001t0001g0161 a0001c0001t0001g0164 a0001c0001t0001g0171 others(15): Show |
19 | HG02056.hp2 HG02145.hp2 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.26+24969A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148612020 | |||||||
chr5:148612326 | G | A | 2 | a0001c0001t0003g0095 a0001c0002t0003g0094 |
2 | HG02717.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.26+24663C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148612326 | |||||||
chr5:148612437 | A | G | 3 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0006g0200 |
3 | HG01361.hp2 HG01433.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.26+24552T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148612437 | |||||||
chr5:148612442 | G | A | 3 | a0001c0001t0005g0143 a0001c0006t0003g0110 a0002c0003t0022g0109 |
3 | HG02148.hp2 HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.26+24547C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148612442 | |||||||
chr5:148612454 | G | A | 1 | a0001c0001t0003g0092 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.26+24535C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148612454 | |||||||
chr5:148612481 | A | G | 3 | a0001c0001t0001g0264 a0001c0001t0001g0267 a0001c0001t0006g0265 |
3 | NA18955.hp2 NA18970.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.26+24508T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148612481 | |||||||
chr5:148612516 | C | T | 18 | a0001c0001t0001g0161 a0001c0001t0001g0164 a0001c0001t0001g0171 others(15): Show |
19 | HG02056.hp2 HG02145.hp2 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.26+24473G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148612516 | |||||||
chr5:148612621 | A | G | 2 | a0001c0001t0010g0083 a0001c0001t0010g0084 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.26+24368T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148612621 | |||||||
chr5:148612698 | T | C | 3 | a0001c0001t0001g0209 a0001c0001t0002g0078 a0001c0001t0002g0079 |
3 | NA18945.hp1 NA18952.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.26+24291A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148612698 | |||||||
chr5:148612857 | G | A | 1 | a0001c0001t0006g0265 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.26+24132C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148612857 | |||||||
chr5:148612907 | C | T | 1 | a0001c0001t0002g0032 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.26+24082G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148612907 | |||||||
chr5:148612963 | T | C | 1 | a0001c0001t0001g0279 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.26+24026A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148612963 | |||||||
chr5:148612984 | A | C | 2 | a0001c0001t0010g0083 a0001c0001t0010g0084 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.26+24005T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148612984 | |||||||
chr5:148613184 | G | A | 2 | a0001c0001t0010g0083 a0001c0001t0010g0084 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.26+23805C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148613184 | |||||||
chr5:148613210 | G | A | 4 | a0001c0001t0008g0134 a0001c0001t0008g0135 a0001c0002t0008g0136 others(1): Show |
4 | HG02922.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.26+23779C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148613210 | |||||||
chr5:148613257 | T | C | 1 | a0001c0001t0001g0196 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.26+23732A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148613257 | |||||||
chr5:148613264 | T | C | 7 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(4): Show |
7 | HG01167.hp1 HG01884.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.26+23725A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148613264 | |||||||
chr5:148613289 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.26+23700G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148613289 | |||||||
chr5:148613299 | A | G | 187 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0164 others(184): Show |
190 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.26+23690T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148613299 | |||||||
chr5:148613379 | C | T | 73 | a0001c0001t0001g0172 a0001c0001t0001g0209 a0001c0001t0001g0249 others(70): Show |
74 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.26+23610G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148613379 | |||||||
chr5:148613421 | G | C | 2 | a0001c0001t0003g0095 a0001c0002t0003g0094 |
2 | HG02717.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.26+23568C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148613421 | |||||||
chr5:148613478 | C | T | 4 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(1): Show |
4 | HG02055.hp1 HG02630.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.26+23511G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148613478 | |||||||
chr5:148613482 | C | T | 2 | a0001c0001t0002g0053 a0001c0001t0002g0054 |
2 | NA18965.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.26+23507G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148613482 | |||||||
chr5:148613558 | A | C | 1 | a0001c0001t0002g0053 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.26+23431T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148613558 | |||||||
chr5:148613575 | T | C | 8 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(5): Show |
8 | HG01167.hp1 HG01884.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.26+23414A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148613575 | |||||||
chr5:148613579 | G | A | 7 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(4): Show |
7 | HG01167.hp1 HG01884.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.26+23410C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148613579 | |||||||
chr5:148613630 | T | A | 18 | a0001c0001t0001g0172 a0001c0001t0002g0020 a0001c0001t0002g0021 others(15): Show |
18 | HG00609.hp2 HG00673.hp1 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.26+23359A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148613630 | |||||||
chr5:148613667 | G | C | 2 | a0001c0001t0010g0083 a0001c0001t0010g0084 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.26+23322C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148613667 | |||||||
chr5:148613721 | G | C | 25 | a0001c0001t0001g0161 a0001c0001t0001g0164 a0001c0001t0001g0171 others(22): Show |
26 | HG01167.hp1 HG01884.hp1 HG02056.hp2 others(23): Show |
intron_variant | MODIFIER | c.26+23268C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148613721 | |||||||
chr5:148613764 | T | C | 69 | a0001c0001t0001g0204 a0001c0001t0001g0250 a0001c0001t0001g0284 others(66): Show |
69 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.26+23225A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148613764 | |||||||
chr5:148613775 | G | T | 4 | a0001c0001t0008g0134 a0001c0001t0008g0135 a0001c0002t0008g0136 others(1): Show |
4 | HG02922.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.26+23214C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148613775 | |||||||
chr5:148613786 | T | C | 3 | a0001c0001t0001g0264 a0001c0001t0001g0267 a0001c0001t0006g0265 |
3 | NA18955.hp2 NA18970.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.26+23203A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148613786 | |||||||
chr5:148613787 | G | A | 3 | a0001c0001t0001g0264 a0001c0001t0001g0267 a0001c0001t0006g0265 |
3 | NA18955.hp2 NA18970.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.26+23202C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148613787 | |||||||
chr5:148614010 | C | T | 4 | a0001c0001t0002g0032 a0001c0001t0003g0119 a0001c0001t0005g0145 others(1): Show |
4 | HG01192.hp2 HG01978.hp2 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.26+22979G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148614010 | |||||||
chr5:148614011 | G | A | 19 | a0001c0001t0001g0161 a0001c0001t0001g0164 a0001c0001t0001g0171 others(16): Show |
20 | HG02056.hp2 HG02145.hp2 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.26+22978C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148614011 | |||||||
chr5:148614200 | C | G | 1 | a0001c0001t0001g0250 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.26+22789G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148614200 | |||||||
chr5:148614307 | C | G | 4 | a0001c0001t0008g0134 a0001c0001t0008g0135 a0001c0002t0008g0136 others(1): Show |
4 | HG02922.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.26+22682G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148614307 | |||||||
chr5:148614322 | A | G | 11 | a0001c0001t0001g0183 a0001c0001t0001g0193 a0001c0001t0001g0195 others(8): Show |
11 | HG01069.hp2 HG01071.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.26+22667T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148614322 | |||||||
chr5:148614379 | A | T | 1 | a0001c0001t0001g0174 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.26+22610T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148614379 | |||||||
chr5:148614386 | C | T | 4 | a0001c0001t0008g0134 a0001c0001t0008g0135 a0001c0002t0008g0136 others(1): Show |
4 | HG02922.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.26+22603G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148614386 | |||||||
chr5:148614422 | G | C | 6 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(3): Show |
6 | HG01167.hp1 HG01884.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.26+22567C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148614422 | |||||||
chr5:148614655 | G | T | 4 | a0001c0001t0008g0134 a0001c0001t0008g0135 a0001c0002t0008g0136 others(1): Show |
4 | HG02922.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.26+22334C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148614655 | |||||||
chr5:148614658 | A | C | 4 | a0001c0001t0008g0134 a0001c0001t0008g0135 a0001c0002t0008g0136 others(1): Show |
4 | HG02922.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.26+22331T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148614658 | |||||||
chr5:148614743 | C | A | 1 | a0001c0001t0003g0113 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.26+22246G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148614743 | |||||||
chr5:148614770 | A | G | 26 | a0001c0001t0001g0161 a0001c0001t0001g0164 a0001c0001t0001g0171 others(23): Show |
27 | HG01167.hp1 HG01884.hp1 HG02056.hp2 others(24): Show |
intron_variant | MODIFIER | c.26+22219T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148614770 | |||||||
chr5:148615122 | C | T | 2 | a0001c0001t0003g0114 a0001c0001t0003g0115 |
2 | HG02886.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.26+21867G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148615122 | |||||||
chr5:148615261 | C | T | 3 | a0001c0001t0001g0277 a0001c0001t0004g0276 a0001c0001t0006g0268 |
3 | NA18991.hp2 NA19011.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.26+21728G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148615261 | |||||||
chr5:148615351 | T | TA | 5 | a0001c0001t0001g0161 a0001c0001t0017g0085 a0001c0002t0001g0160 others(2): Show |
5 | HG02145.hp2 HG02451.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.26+21637dupT | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148615351 | |||||||
chr5:148615402 | T | A | 25 | a0001c0001t0001g0161 a0001c0001t0001g0164 a0001c0001t0001g0171 others(22): Show |
26 | HG01167.hp1 HG01884.hp1 HG02056.hp2 others(23): Show |
intron_variant | MODIFIER | c.26+21587A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148615402 | |||||||
chr5:148615424 | A | G | 1 | a0001c0001t0010g0086 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.26+21565T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148615424 | |||||||
chr5:148615542 | A | G | 2 | a0001c0001t0001g0281 a0001c0001t0001g0282 |
2 | HG03669.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.26+21447T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148615542 | |||||||
chr5:148615563 | GAGATATA others(4): Show |
G | 7 | a0001c0001t0003g0100 a0001c0001t0003g0101 a0001c0001t0003g0102 others(4): Show |
7 | HG01496.hp2 HG01884.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.26+21415_26+21425d others(13): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148615563 | |||||||
chr5:148615681 | A | G | 18 | a0001c0001t0001g0172 a0001c0001t0002g0020 a0001c0001t0002g0021 others(15): Show |
18 | HG00609.hp2 HG00673.hp1 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.26+21308T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148615681 | |||||||
chr5:148615692 | TAAAG | T | 7 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(4): Show |
7 | HG01167.hp1 HG01884.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.26+21293_26+21296d others(6): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148615692 | |||||||
chr5:148615696 | G | T | 21 | a0001c0001t0001g0161 a0001c0001t0001g0164 a0001c0001t0001g0171 others(18): Show |
22 | HG02056.hp2 HG02145.hp2 HG02451.hp2 others(19): Show |
intron_variant | MODIFIER | c.26+21293C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148615696 | |||||||
chr5:148615700 | G | T | 7 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(4): Show |
7 | HG01167.hp1 HG01884.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.26+21289C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148615700 | |||||||
chr5:148615704 | G | T | 5 | a0001c0001t0008g0134 a0001c0001t0008g0135 a0001c0002t0003g0088 others(2): Show |
5 | HG02647.hp2 HG02922.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.26+21285C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148615704 | |||||||
chr5:148615707 | A | AT | 11 | a0001c0001t0001g0164 a0001c0001t0001g0176 a0001c0001t0001g0248 others(8): Show |
12 | HG03017.hp2 HG03710.hp2 NA18947.hp2 others(9): Show |
intron_variant | MODIFIER | c.26+21281_26+21282i others(3): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148615707 | |||||||
chr5:148615707 | A | ATAAAAT | 7 | a0001c0001t0001g0161 a0001c0001t0001g0171 a0001c0001t0001g0179 others(4): Show |
7 | HG02056.hp2 HG02145.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.26+21281_26+21282i others(8): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148615707 | |||||||
chr5:148615707 | A | ATAAATAA others(3): Show |
2 | a0001c0002t0008g0136 a0001c0002t0008g0137 |
2 | HG02922.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.26+21281_26+21282i others(12): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148615707 | |||||||
chr5:148615707 | A | ATAAATAA others(8): Show |
1 | a0001c0001t0008g0134 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.26+21281_26+21282i others(17): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148615707 | |||||||
chr5:148615708 | G | A | 22 | a0001c0001t0001g0161 a0001c0001t0001g0164 a0001c0001t0001g0171 others(19): Show |
23 | HG02056.hp2 HG02145.hp2 HG02451.hp2 others(20): Show |
intron_variant | MODIFIER | c.26+21281C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148615708 | |||||||
chr5:148615708 | G | GAAATA | 65 | a0001c0001t0001g0201 a0001c0001t0001g0209 a0001c0001t0001g0239 others(62): Show |
66 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.26+21276_26+21280d others(7): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148615708 | |||||||
chr5:148615708 | G | GAAATAAA others(3): Show |
20 | a0001c0001t0001g0172 a0001c0001t0002g0020 a0001c0001t0002g0021 others(17): Show |
20 | HG00609.hp2 HG00673.hp1 HG01928.hp2 others(17): Show |
intron_variant | MODIFIER | c.26+21271_26+21280d others(12): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148615708 | |||||||
chr5:148615708 | G | T | 2 | a0001c0001t0001g0203 a0001c0001t0001g0260 |
2 | NA18967.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.26+21281C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148615708 | |||||||
chr5:148615713 | A | T | 1 | a0001c0002t0003g0088 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.26+21276T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148615713 | |||||||
chr5:148615813 | C | T | 3 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 |
3 | HG00099.hp2 HG00323.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.26+21176G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148615813 | |||||||
chr5:148615851 | C | G | 13 | a0001c0001t0001g0202 a0001c0001t0001g0211 a0001c0001t0001g0213 others(10): Show |
13 | HG01243.hp2 HG02055.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.26+21138G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148615851 | |||||||
chr5:148615861 | A | G | 5 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0190 others(2): Show |
6 | HG01891.hp1 HG02818.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.26+21128T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148615861 | |||||||
chr5:148615898 | C | T | 3 | a0001c0001t0003g0095 a0001c0001t0003g0112 a0001c0002t0003g0094 |
3 | HG02630.hp2 HG02717.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.26+21091G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148615898 | |||||||
chr5:148616042 | T | C | 72 | a0001c0001t0001g0172 a0001c0001t0001g0209 a0001c0001t0001g0249 others(69): Show |
73 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.26+20947A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148616042 | |||||||
chr5:148616127 | A | T | 18 | a0001c0001t0001g0172 a0001c0001t0002g0020 a0001c0001t0002g0021 others(15): Show |
18 | HG00609.hp2 HG00673.hp1 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.26+20862T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148616127 | |||||||
chr5:148616524 | T | C | 233 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0164 others(230): Show |
236 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.26+20465A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148616524 | |||||||
chr5:148616557 | T | C | 1 | a0001c0001t0006g0240 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.26+20432A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148616557 | |||||||
chr5:148616566 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.26+20423G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148616566 | |||||||
chr5:148616584 | A | C | 2 | a0001c0001t0001g0225 a0001c0004t0001g0242 |
2 | HG02300.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.26+20405T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148616584 | |||||||
chr5:148616767 | AT | A | 53 | a0001c0001t0001g0209 a0001c0001t0001g0249 a0001c0001t0001g0253 others(50): Show |
54 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.26+20221delA | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148616767 | |||||||
chr5:148616842 | A | C | 2 | a0001c0001t0001g0299 a0001c0001t0001g0300 |
2 | HG00741.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.26+20147T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148616842 | |||||||
chr5:148617092 | G | A | 5 | a0001c0001t0002g0044 a0001c0001t0002g0049 a0001c0001t0002g0050 others(2): Show |
5 | HG00408.hp2 HG00438.hp2 NA18949.hp1 others(2): Show |
intron_variant | MODIFIER | c.26+19897C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148617092 | |||||||
chr5:148617141 | T | C | 18 | a0001c0001t0001g0172 a0001c0001t0002g0020 a0001c0001t0002g0021 others(15): Show |
18 | HG00609.hp2 HG00673.hp1 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.26+19848A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148617141 | |||||||
chr5:148617196 | G | A | 1 | a0001c0001t0004g0170 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.26+19793C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148617196 | |||||||
chr5:148617295 | G | T | 1 | a0001c0001t0002g0053 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.26+19694C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148617295 | |||||||
chr5:148617325 | C | T | 71 | a0001c0001t0001g0172 a0001c0001t0001g0209 a0001c0001t0001g0249 others(68): Show |
72 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.26+19664G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148617325 | |||||||
chr5:148617360 | T | G | 18 | a0001c0001t0001g0172 a0001c0001t0002g0020 a0001c0001t0002g0021 others(15): Show |
18 | HG00609.hp2 HG00673.hp1 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.26+19629A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148617360 | |||||||
chr5:148617366 | T | C | 1 | a0001c0001t0001g0171 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.26+19623A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148617366 | |||||||
chr5:148617469 | TTTTTTTT others(2): Show |
T | 53 | a0001c0001t0001g0209 a0001c0001t0001g0249 a0001c0001t0001g0253 others(50): Show |
54 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.26+19511_26+19519d others(11): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148617469 | |||||||
chr5:148617477 | T | TTG | 25 | a0001c0001t0001g0161 a0001c0001t0001g0164 a0001c0001t0001g0171 others(22): Show |
26 | HG01167.hp1 HG01884.hp1 HG02056.hp2 others(23): Show |
intron_variant | MODIFIER | c.26+19511_26+19512i others(4): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148617477 | |||||||
chr5:148617478 | G | GT | 21 | a0001c0001t0001g0172 a0001c0001t0002g0020 a0001c0001t0002g0021 others(18): Show |
21 | HG00609.hp2 HG00673.hp1 HG01928.hp2 others(18): Show |
intron_variant | MODIFIER | c.26+19510dupA | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148617478 | |||||||
chr5:148617478 | G | T | 26 | a0001c0001t0001g0161 a0001c0001t0001g0164 a0001c0001t0001g0171 others(23): Show |
27 | HG01167.hp1 HG01884.hp1 HG02056.hp2 others(24): Show |
intron_variant | MODIFIER | c.26+19511C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148617478 | |||||||
chr5:148617530 | G | A | 1 | a0001c0001t0001g0288 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.26+19459C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148617530 | |||||||
chr5:148617592 | C | T | 1 | a0001c0001t0001g0224 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.26+19397G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148617592 | |||||||
chr5:148617629 | C | A | 1 | a0001c0001t0001g0243 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.26+19360G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148617629 | |||||||
chr5:148617714 | G | A | 1 | a0001c0001t0002g0045 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.26+19275C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148617714 | |||||||
chr5:148617816 | G | T | 3 | a0001c0001t0001g0245 a0001c0001t0001g0246 a0001c0001t0001g0247 |
3 | HG01069.hp2 HG01071.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.26+19173C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148617816 | |||||||
chr5:148617883 | G | A | 1 | a0001c0001t0014g0004 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.26+19106C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148617883 | |||||||
chr5:148617922 | T | C | 6 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0192 others(3): Show |
6 | HG01243.hp1 HG01361.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.26+19067A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148617922 | |||||||
chr5:148618015 | G | A | 10 | a0001c0001t0001g0164 a0001c0001t0001g0179 a0001c0001t0001g0248 others(7): Show |
11 | HG02056.hp2 NA18947.hp2 NA18962.hp1 others(8): Show |
intron_variant | MODIFIER | c.26+18974C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148618015 | |||||||
chr5:148618034 | C | G | 32 | a0001c0001t0001g0204 a0001c0001t0002g0008 a0001c0001t0002g0011 others(29): Show |
32 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.26+18955G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148618034 | |||||||
chr5:148618036 | T | A | 32 | a0001c0001t0001g0204 a0001c0001t0002g0008 a0001c0001t0002g0011 others(29): Show |
32 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.26+18953A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148618036 | |||||||
chr5:148618038 | AG | A | 32 | a0001c0001t0001g0204 a0001c0001t0002g0008 a0001c0001t0002g0011 others(29): Show |
32 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.26+18950delC | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148618038 | |||||||
chr5:148618069 | A | T | 1 | a0001c0001t0026g0184 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.26+18920T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148618069 | |||||||
chr5:148618213 | G | A | 1 | a0001c0001t0006g0175 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.26+18776C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148618213 | |||||||
chr5:148618250 | A | G | 1 | a0001c0001t0005g0145 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.26+18739T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148618250 | |||||||
chr5:148618503 | C | T | 1 | a0001c0001t0001g0164 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.26+18486G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148618503 | |||||||
chr5:148618556 | G | A | 71 | a0001c0001t0001g0204 a0001c0001t0001g0250 a0001c0001t0001g0251 others(68): Show |
71 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.26+18433C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148618556 | |||||||
chr5:148618581 | G | C | 1 | a0001c0001t0006g0241 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.26+18408C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148618581 | |||||||
chr5:148618644 | TC | T | 77 | a0001c0001t0001g0204 a0001c0001t0001g0250 a0001c0001t0001g0251 others(74): Show |
77 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.26+18344delG | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148618644 | |||||||
chr5:148618668 | C | T | 1 | a0001c0001t0004g0298 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.26+18321G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148618668 | |||||||
chr5:148618813 | A | T | 53 | a0001c0001t0001g0209 a0001c0001t0001g0249 a0001c0001t0001g0253 others(50): Show |
54 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.26+18176T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148618813 | |||||||
chr5:148618928 | A | G | 202 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0164 others(199): Show |
205 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.26+18061T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148618928 | |||||||
chr5:148619016 | G | T | 233 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0164 others(230): Show |
236 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.26+17973C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148619016 | |||||||
chr5:148619147 | A | G | 4 | a0001c0001t0008g0134 a0001c0001t0008g0135 a0001c0002t0008g0136 others(1): Show |
4 | HG02922.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.26+17842T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148619147 | |||||||
chr5:148619293 | A | G | 1 | a0001c0001t0005g0152 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.26+17696T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148619293 | |||||||
chr5:148619340 | G | A | 3 | a0001c0001t0001g0209 a0001c0001t0002g0078 a0001c0001t0002g0079 |
3 | NA18945.hp1 NA18952.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.26+17649C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148619340 | |||||||
chr5:148619452 | TAAGTTA | T | 26 | a0001c0001t0001g0161 a0001c0001t0001g0164 a0001c0001t0001g0171 others(23): Show |
27 | HG01167.hp1 HG01884.hp1 HG02056.hp2 others(24): Show |
intron_variant | MODIFIER | c.26+17531_26+17536d others(8): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148619452 | |||||||
chr5:148619508 | CT | C | 3 | a0001c0001t0001g0198 a0001c0001t0001g0243 a0001c0002t0001g0197 |
3 | HG02257.hp1 HG02723.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.26+17480delA | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148619508 | |||||||
chr5:148619769 | A | T | 2 | a0001c0001t0002g0011 a0001c0001t0002g0012 |
2 | NA18998.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.26+17220T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148619769 | |||||||
chr5:148620187 | G | A | 5 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0190 others(2): Show |
6 | HG01891.hp1 HG02818.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.26+16802C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148620187 | |||||||
chr5:148620340 | T | C | 2 | a0001c0001t0002g0046 a0001c0001t0002g0047 |
2 | HG02486.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.26+16649A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148620340 | |||||||
chr5:148620361 | G | A | 3 | a0001c0001t0001g0245 a0001c0001t0001g0246 a0001c0001t0001g0247 |
3 | HG01069.hp2 HG01071.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.26+16628C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148620361 | |||||||
chr5:148620466 | G | A | 18 | a0001c0001t0001g0172 a0001c0001t0002g0020 a0001c0001t0002g0021 others(15): Show |
18 | HG00609.hp2 HG00673.hp1 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.26+16523C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148620466 | |||||||
chr5:148620754 | A | G | 5 | a0001c0001t0001g0183 a0001c0001t0001g0193 a0001c0001t0001g0195 others(2): Show |
5 | HG02055.hp2 HG02486.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.26+16235T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148620754 | |||||||
chr5:148621170 | A | G | 1 | a0001c0001t0015g0014 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.26+15819T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148621170 | |||||||
chr5:148621782 | ATTTCCT | A | 4 | a0001c0001t0002g0049 a0001c0001t0002g0050 a0001c0001t0007g0048 others(1): Show |
4 | HG00408.hp2 HG00438.hp2 NA18949.hp1 others(1): Show |
intron_variant | MODIFIER | c.26+15201_26+15206d others(8): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148621782 | |||||||
chr5:148621879 | G | C | 1 | a0001c0001t0004g0298 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.26+15110C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148621879 | |||||||
chr5:148621898 | A | G | 1 | a0001c0001t0001g0253 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.26+15091T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148621898 | |||||||
chr5:148621907 | T | C | 54 | a0001c0001t0001g0209 a0001c0001t0001g0249 a0001c0001t0001g0253 others(51): Show |
55 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.26+15082A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148621907 | |||||||
chr5:148622049 | G | C | 13 | a0001c0001t0001g0202 a0001c0001t0001g0211 a0001c0001t0001g0213 others(10): Show |
13 | HG01243.hp2 HG02055.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.26+14940C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148622049 | |||||||
chr5:148622762 | G | A | 25 | a0001c0001t0001g0161 a0001c0001t0001g0164 a0001c0001t0001g0171 others(22): Show |
26 | HG01167.hp1 HG01884.hp1 HG02056.hp2 others(23): Show |
intron_variant | MODIFIER | c.26+14227C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148622762 | |||||||
chr5:148622771 | T | A | 1 | a0001c0002t0003g0088 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.26+14218A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148622771 | |||||||
chr5:148622891 | T | A | 25 | a0001c0001t0001g0161 a0001c0001t0001g0164 a0001c0001t0001g0171 others(22): Show |
26 | HG01167.hp1 HG01884.hp1 HG02056.hp2 others(23): Show |
intron_variant | MODIFIER | c.26+14098A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148622891 | |||||||
chr5:148623117 | A | C | 1 | a0001c0001t0006g0175 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.26+13872T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148623117 | |||||||
chr5:148623291 | A | G | 5 | a0001c0001t0008g0134 a0001c0001t0008g0135 a0001c0002t0003g0088 others(2): Show |
5 | HG02647.hp2 HG02922.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.26+13698T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148623291 | |||||||
chr5:148623779 | C | T | 3 | a0001c0001t0001g0198 a0001c0001t0001g0243 a0001c0002t0001g0197 |
3 | HG02257.hp1 HG02723.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.26+13210G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148623779 | |||||||
chr5:148623917 | G | A | 4 | a0001c0001t0008g0134 a0001c0001t0008g0135 a0001c0002t0008g0136 others(1): Show |
4 | HG02922.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.26+13072C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148623917 | |||||||
chr5:148624236 | G | C | 1 | a0001c0001t0002g0010 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.26+12753C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148624236 | |||||||
chr5:148624400 | A | C | 1 | a0001c0002t0003g0088 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.26+12589T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148624400 | |||||||
chr5:148624669 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.26+12320G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148624669 | |||||||
chr5:148624680 | C | T | 1 | a0001c0001t0003g0113 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.26+12309G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148624680 | |||||||
chr5:148624872 | T | C | 2 | a0001c0001t0004g0255 a0001c0001t0004g0256 |
2 | NA18943.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.26+12117A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148624872 | |||||||
chr5:148625155 | G | A | 1 | a0001c0001t0001g0201 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.26+11834C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148625155 | |||||||
chr5:148625190 | A | T | 1 | a0001c0001t0010g0086 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.26+11799T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148625190 | |||||||
chr5:148625684 | G | A | 4 | a0001c0001t0003g0090 a0001c0001t0003g0091 a0001c0001t0003g0092 others(1): Show |
4 | HG02258.hp1 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.26+11305C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148625684 | |||||||
chr5:148625886 | C | CT | 12 | a0001c0001t0001g0183 a0001c0001t0001g0193 a0001c0001t0001g0195 others(9): Show |
12 | HG01192.hp2 HG01978.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.26+11102dupA | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148625886 | |||||||
chr5:148626511 | T | A | 4 | a0001c0001t0001g0003 a0001c0001t0001g0190 a0001c0001t0001g0191 others(1): Show |
5 | HG01891.hp1 HG02965.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.26+10478A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148626511 | |||||||
chr5:148626687 | C | T | 2 | a0001c0001t0003g0114 a0001c0001t0003g0115 |
2 | HG02886.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.26+10302G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148626687 | |||||||
chr5:148626699 | A | T | 53 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0252 others(50): Show |
53 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.26+10290T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148626699 | |||||||
chr5:148626709 | G | A | 7 | a0001c0001t0003g0100 a0001c0001t0003g0101 a0001c0001t0003g0102 others(4): Show |
7 | HG01496.hp2 HG01884.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.26+10280C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148626709 | |||||||
chr5:148627018 | C | A | 2 | a0001c0001t0001g0277 a0001c0001t0004g0276 |
2 | NA19011.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.26+9971G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148627018 | |||||||
chr5:148627041 | A | T | 1 | a0001c0001t0006g0212 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.26+9948T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148627041 | |||||||
chr5:148627188 | T | C | 1 | a0003c0009t0027g0307 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.26+9801A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148627188 | |||||||
chr5:148627309 | A | T | 17 | a0001c0001t0001g0172 a0001c0001t0002g0020 a0001c0001t0002g0021 others(14): Show |
17 | HG00609.hp2 HG00673.hp1 HG01928.hp2 others(14): Show |
intron_variant | MODIFIER | c.26+9680T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148627309 | |||||||
chr5:148627338 | G | A | 76 | a0001c0001t0001g0204 a0001c0001t0001g0209 a0001c0001t0001g0249 others(73): Show |
76 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.26+9651C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148627338 | |||||||
chr5:148627342 | AT | A | 76 | a0001c0001t0001g0204 a0001c0001t0001g0209 a0001c0001t0001g0249 others(73): Show |
76 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.26+9646delA | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148627342 | |||||||
chr5:148627344 | T | C | 76 | a0001c0001t0001g0204 a0001c0001t0001g0209 a0001c0001t0001g0249 others(73): Show |
76 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.26+9645A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148627344 | |||||||
chr5:148627367 | T | G | 1 | a0001c0004t0001g0242 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.26+9622A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148627367 | |||||||
chr5:148627383 | C | A | 84 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(81): Show |
84 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.26+9606G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148627383 | |||||||
chr5:148627390 | C | T | 84 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(81): Show |
84 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.26+9599G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148627390 | |||||||
chr5:148627450 | G | A | 181 | a0001c0001t0001g0161 a0001c0001t0001g0164 a0001c0001t0001g0171 others(178): Show |
183 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.26+9539C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148627450 | |||||||
chr5:148627589 | T | C | 1 | a0001c0001t0003g0119 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.26+9400A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148627589 | |||||||
chr5:148627680 | T | C | 2 | a0001c0001t0001g0278 a0001c0001t0001g0279 |
2 | NA19000.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.26+9309A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148627680 | |||||||
chr5:148627690 | A | G | 1 | a0001c0001t0005g0148 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.26+9299T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148627690 | |||||||
chr5:148627826 | C | T | 1 | a0001c0001t0012g0205 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.26+9163G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148627826 | |||||||
chr5:148628102 | T | A | 1 | a0001c0001t0024g0154 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.26+8887A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148628102 | |||||||
chr5:148628149 | T | C | 6 | a0001c0001t0002g0013 a0001c0001t0002g0015 a0001c0001t0002g0016 others(3): Show |
6 | HG00099.hp2 HG00323.hp1 HG00741.hp2 others(3): Show |
intron_variant | MODIFIER | c.26+8840A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148628149 | |||||||
chr5:148628261 | G | T | 1 | a0001c0001t0002g0031 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.26+8728C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148628261 | |||||||
chr5:148628297 | C | A | 181 | a0001c0001t0001g0161 a0001c0001t0001g0164 a0001c0001t0001g0171 others(178): Show |
183 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.26+8692G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148628297 | |||||||
chr5:148628502 | T | G | 3 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0006g0200 |
3 | HG01361.hp2 HG01433.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.26+8487A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148628502 | |||||||
chr5:148628757 | T | A | 1 | a0001c0001t0024g0154 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.26+8232A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148628757 | |||||||
chr5:148628858 | T | G | 22 | a0001c0001t0001g0161 a0001c0001t0001g0164 a0001c0001t0001g0171 others(19): Show |
24 | HG01071.hp1 HG01074.hp2 HG02056.hp2 others(21): Show |
intron_variant | MODIFIER | c.26+8131A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148628858 | |||||||
chr5:148629028 | C | T | 22 | a0001c0001t0001g0161 a0001c0001t0001g0164 a0001c0001t0001g0171 others(19): Show |
24 | HG01071.hp1 HG01074.hp2 HG02056.hp2 others(21): Show |
intron_variant | MODIFIER | c.26+7961G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148629028 | |||||||
chr5:148629044 | C | T | 1 | a0001c0001t0001g0269 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.26+7945G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148629044 | |||||||
chr5:148629538 | G | A | 47 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0252 others(44): Show |
47 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.26+7451C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148629538 | |||||||
chr5:148629567 | G | C | 2 | a0001c0001t0002g0057 a0001c0001t0002g0058 |
2 | NA18941.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.26+7422C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148629567 | |||||||
chr5:148629831 | C | T | 11 | a0001c0001t0002g0008 a0001c0001t0003g0095 a0001c0001t0003g0099 others(8): Show |
11 | HG00438.hp1 HG00558.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.26+7158G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148629831 | |||||||
chr5:148629851 | T | C | 1 | a0001c0001t0001g0267 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.26+7138A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148629851 | |||||||
chr5:148629918 | G | A | 1 | a0001c0001t0001g0280 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.26+7071C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148629918 | |||||||
chr5:148629961 | A | G | 13 | a0001c0001t0002g0020 a0001c0001t0002g0021 a0001c0001t0002g0022 others(10): Show |
13 | HG00609.hp2 HG01928.hp2 HG01952.hp2 others(10): Show |
intron_variant | MODIFIER | c.26+7028T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148629961 | |||||||
chr5:148630485 | C | A | 7 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(4): Show |
7 | HG01167.hp1 HG01884.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.26+6504G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148630485 | |||||||
chr5:148630506 | G | A | 185 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0164 others(182): Show |
188 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.26+6483C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148630506 | |||||||
chr5:148630566 | C | T | 3 | a0001c0001t0003g0132 a0001c0001t0003g0133 a0001c0001t0005g0001 |
4 | HG01071.hp1 HG01074.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.26+6423G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148630566 | |||||||
chr5:148630573 | T | C | 1 | a0001c0001t0009g0157 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.26+6416A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148630573 | |||||||
chr5:148630630 | A | G | 4 | a0001c0001t0001g0003 a0001c0001t0001g0190 a0001c0001t0001g0191 others(1): Show |
5 | HG01891.hp1 HG02965.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.26+6359T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148630630 | |||||||
chr5:148631219 | T | C | 4 | a0001c0001t0008g0134 a0001c0001t0008g0135 a0001c0002t0008g0136 others(1): Show |
4 | HG02922.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.26+5770A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148631219 | |||||||
chr5:148631350 | G | A | 78 | a0001c0001t0001g0204 a0001c0001t0001g0209 a0001c0001t0001g0249 others(75): Show |
78 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.26+5639C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148631350 | |||||||
chr5:148631549 | C | T | 1 | a0001c0001t0003g0127 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.26+5440G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148631549 | |||||||
chr5:148631608 | G | T | 4 | a0001c0001t0008g0134 a0001c0001t0008g0135 a0001c0002t0008g0136 others(1): Show |
4 | HG02922.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.26+5381C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148631608 | |||||||
chr5:148631644 | A | T | 1 | a0001c0001t0002g0019 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.26+5345T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148631644 | |||||||
chr5:148631771 | G | C | 3 | a0001c0001t0001g0281 a0001c0001t0001g0282 a0001c0001t0001g0283 |
3 | HG03239.hp2 HG03669.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.26+5218C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148631771 | |||||||
chr5:148631792 | C | T | 1 | a0001c0001t0006g0268 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.26+5197G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148631792 | |||||||
chr5:148632009 | G | A | 1 | a0001c0001t0002g0010 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.26+4980C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148632009 | |||||||
chr5:148632167 | C | T | 2 | a0001c0001t0002g0011 a0001c0001t0002g0012 |
2 | NA18998.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.26+4822G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148632167 | |||||||
chr5:148632172 | C | T | 1 | a0001c0001t0001g0249 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.26+4817G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148632172 | |||||||
chr5:148632176 | T | C | 235 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0164 others(232): Show |
238 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(235): Show |
intron_variant | MODIFIER | c.26+4813A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148632176 | |||||||
chr5:148632299 | C | T | 1 | a0001c0001t0001g0211 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.26+4690G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148632299 | |||||||
chr5:148632393 | C | T | 161 | a0001c0001t0001g0172 a0001c0001t0001g0185 a0001c0001t0001g0186 others(158): Show |
161 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.26+4596G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148632393 | |||||||
chr5:148632411 | C | G | 1 | a0001c0001t0002g0030 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.26+4578G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148632411 | |||||||
chr5:148632483 | A | G | 1 | a0001c0001t0006g0223 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.26+4506T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148632483 | |||||||
chr5:148632496 | G | A | 2 | a0001c0001t0001g0192 a0003c0009t0027g0307 |
2 | HG01243.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.26+4493C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148632496 | |||||||
chr5:148632664 | T | C | 4 | a0001c0001t0008g0134 a0001c0001t0008g0135 a0001c0002t0008g0136 others(1): Show |
4 | HG02922.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.26+4325A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148632664 | |||||||
chr5:148632742 | G | A | 7 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(4): Show |
7 | HG01167.hp1 HG01884.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.26+4247C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148632742 | |||||||
chr5:148632746 | G | GA | 4 | a0001c0001t0008g0134 a0001c0001t0008g0135 a0001c0002t0008g0136 others(1): Show |
4 | HG02922.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.26+4242dupT | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148632746 | |||||||
chr5:148632849 | A | C | 1 | a0001c0001t0005g0145 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.26+4140T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148632849 | |||||||
chr5:148632851 | A | G | 4 | a0001c0001t0008g0134 a0001c0001t0008g0135 a0001c0002t0008g0136 others(1): Show |
4 | HG02922.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.26+4138T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148632851 | |||||||
chr5:148632860 | T | C | 1 | a0001c0001t0003g0126 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.26+4129A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148632860 | |||||||
chr5:148632990 | A | C | 4 | a0001c0001t0008g0134 a0001c0001t0008g0135 a0001c0002t0008g0136 others(1): Show |
4 | HG02922.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.26+3999T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148632990 | |||||||
chr5:148633126 | G | A | 1 | a0001c0001t0001g0292 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.26+3863C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148633126 | |||||||
chr5:148633164 | A | T | 2 | a0001c0001t0010g0083 a0001c0001t0010g0084 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.26+3825T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148633164 | |||||||
chr5:148633353 | C | T | 5 | a0001c0001t0001g0003 a0001c0001t0001g0190 a0001c0001t0001g0191 others(2): Show |
6 | HG01891.hp1 HG02698.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.26+3636G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148633353 | |||||||
chr5:148633382 | C | CT | 128 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(125): Show |
128 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.26+3606dupA | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148633382 | |||||||
chr5:148633486 | A | G | 152 | a0001c0001t0001g0172 a0001c0001t0001g0185 a0001c0001t0001g0186 others(149): Show |
152 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.26+3503T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148633486 | |||||||
chr5:148633528 | C | G | 1 | a0001c0001t0001g0172 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.26+3461G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148633528 | |||||||
chr5:148633539 | C | T | 2 | a0001c0006t0003g0110 a0002c0003t0022g0109 |
2 | HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.26+3450G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148633539 | |||||||
chr5:148633612 | G | A | 1 | a0001c0001t0010g0086 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.26+3377C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148633612 | |||||||
chr5:148633625 | C | T | 13 | a0001c0001t0001g0202 a0001c0001t0001g0211 a0001c0001t0001g0213 others(10): Show |
13 | HG01243.hp2 HG02055.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.26+3364G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148633625 | |||||||
chr5:148633890 | G | C | 17 | a0001c0001t0001g0172 a0001c0001t0002g0020 a0001c0001t0002g0021 others(14): Show |
17 | HG00609.hp2 HG00673.hp1 HG01928.hp2 others(14): Show |
intron_variant | MODIFIER | c.26+3099C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148633890 | |||||||
chr5:148634166 | C | A | 1 | a0001c0001t0006g0200 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.26+2823G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148634166 | |||||||
chr5:148634179 | G | C | 142 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(139): Show |
142 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.26+2810C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148634179 | |||||||
chr5:148634215 | T | C | 1 | a0001c0001t0003g0112 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.26+2774A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148634215 | |||||||
chr5:148634335 | G | A | 2 | a0001c0002t0001g0162 a0001c0002t0003g0089 |
2 | HG02145.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.26+2654C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148634335 | |||||||
chr5:148634424 | T | C | 3 | a0001c0001t0002g0053 a0001c0001t0002g0054 a0001c0001t0002g0055 |
3 | NA18965.hp1 NA19067.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.26+2565A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148634424 | |||||||
chr5:148634553 | T | A | 3 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0006g0200 |
3 | HG01361.hp2 HG01433.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.26+2436A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148634553 | |||||||
chr5:148634704 | T | C | 2 | a0001c0001t0001g0198 a0001c0002t0001g0197 |
2 | HG02257.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.26+2285A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148634704 | |||||||
chr5:148635022 | C | T | 4 | a0001c0001t0001g0003 a0001c0001t0001g0190 a0001c0001t0001g0191 others(1): Show |
5 | HG01891.hp1 HG02965.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.26+1967G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148635022 | |||||||
chr5:148635050 | C | A | 6 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(3): Show |
6 | HG01884.hp1 HG02622.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.26+1939G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148635050 | |||||||
chr5:148635344 | T | C | 4 | a0001c0001t0008g0134 a0001c0001t0008g0135 a0001c0002t0008g0136 others(1): Show |
4 | HG02922.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.26+1645A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148635344 | |||||||
chr5:148635463 | A | G | 1 | a0001c0001t0012g0205 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.26+1526T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148635463 | |||||||
chr5:148635554 | T | C | 1 | a0001c0001t0002g0056 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.26+1435A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148635554 | |||||||
chr5:148635678 | A | G | 2 | a0001c0001t0004g0158 a0001c0001t0004g0259 |
2 | NA19011.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.26+1311T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148635678 | |||||||
chr5:148635922 | A | T | 4 | a0001c0001t0003g0090 a0001c0001t0003g0091 a0001c0001t0003g0092 others(1): Show |
4 | HG02258.hp1 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.26+1067T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148635922 | |||||||
chr5:148635941 | A | G | 3 | a0001c0001t0009g0155 a0001c0001t0009g0156 a0001c0001t0009g0157 |
3 | HG02559.hp1 HG02809.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.26+1048T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148635941 | |||||||
chr5:148636206 | T | C | 4 | a0001c0001t0008g0134 a0001c0001t0008g0135 a0001c0002t0008g0136 others(1): Show |
4 | HG02922.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.26+783A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148636206 | |||||||
chr5:148636240 | A | C | 2 | a0001c0001t0001g0199 a0001c0001t0006g0200 |
2 | HG02145.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.26+749T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148636240 | |||||||
chr5:148636355 | A | C | 3 | a0001c0001t0010g0083 a0001c0001t0010g0084 a0001c0001t0017g0085 |
3 | HG02896.hp1 HG02897.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.26+634T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148636355 | |||||||
chr5:148636430 | T | C | 1 | a0001c0001t0001g0289 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.26+559A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148636430 | |||||||
chr5:148636501 | G | A | 13 | a0001c0001t0002g0005 a0001c0001t0003g0120 a0001c0001t0003g0121 others(10): Show |
14 | HG00140.hp2 HG01071.hp1 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.26+488C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148636501 | |||||||
chr5:148636556 | C | A | 1 | a0001c0001t0003g0093 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.26+433G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148636556 | |||||||
chr5:148636632 | C | T | 5 | a0001c0001t0002g0008 a0001c0001t0003g0096 a0001c0001t0003g0097 others(2): Show |
5 | NA18951.hp2 NA18975.hp2 NA19001.hp2 others(2): Show |
intron_variant | MODIFIER | c.26+357G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148636632 | |||||||
chr5:148636801 | C | T | 2 | a0001c0006t0003g0110 a0002c0003t0022g0109 |
2 | HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.26+188G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148636801 | |||||||
chr5:148636868 | T | C | 2 | a0001c0002t0008g0136 a0001c0002t0008g0137 |
2 | HG02922.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.26+121A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148636868 | |||||||
chr5:148636974 | A | G | 13 | a0001c0001t0002g0005 a0001c0001t0003g0120 a0001c0001t0003g0121 others(10): Show |
14 | HG00140.hp2 HG01071.hp1 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.26+15T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | 148636974 | |||||||
chr5:148637073 | G | A | 1 | a0001c0001t0005g0148 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-47-12C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148637073 | |||||||
chr5:148637184 | A | G | 1 | a0001c0001t0006g0257 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-47-123T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148637184 | |||||||
chr5:148637200 | C | T | 1 | a0001c0001t0001g0210 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-47-139G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148637200 | |||||||
chr5:148637222 | C | T | 4 | a0001c0001t0008g0134 a0001c0001t0008g0135 a0001c0002t0008g0136 others(1): Show |
4 | HG02922.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47-161G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148637222 | |||||||
chr5:148637291 | T | C | 4 | a0001c0001t0003g0090 a0001c0001t0003g0091 a0001c0001t0003g0092 others(1): Show |
4 | HG02258.hp1 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-47-230A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148637291 | |||||||
chr5:148637294 | G | T | 160 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0163 others(157): Show |
163 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.-47-233C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148637294 | |||||||
chr5:148637362 | G | T | 4 | a0001c0001t0008g0134 a0001c0001t0008g0135 a0001c0002t0008g0136 others(1): Show |
4 | HG02922.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47-301C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148637362 | |||||||
chr5:148637377 | T | C | 4 | a0001c0001t0008g0134 a0001c0001t0008g0135 a0001c0002t0008g0136 others(1): Show |
4 | HG02922.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47-316A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148637377 | |||||||
chr5:148637421 | TTGCCCAA others(2): Show |
T | 23 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0164 others(20): Show |
24 | HG01361.hp2 HG01433.hp1 HG02056.hp2 others(21): Show |
intron_variant | MODIFIER | c.-47-369_-47-361del others(9): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148637421 | |||||||
chr5:148637432 | G | C | 1 | a0001c0001t0005g0143 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-47-371C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148637432 | |||||||
chr5:148637446 | T | C | 4 | a0001c0001t0008g0134 a0001c0001t0008g0135 a0001c0002t0008g0136 others(1): Show |
4 | HG02922.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47-385A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148637446 | |||||||
chr5:148637457 | T | TA | 4 | a0001c0001t0008g0134 a0001c0001t0008g0135 a0001c0002t0008g0136 others(1): Show |
4 | HG02922.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47-397dupT | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148637457 | |||||||
chr5:148637861 | C | T | 5 | a0001c0001t0009g0156 a0001c0001t0009g0157 a0001c0001t0010g0083 others(2): Show |
5 | HG02559.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-47-800G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148637861 | |||||||
chr5:148637874 | T | C | 4 | a0001c0001t0008g0134 a0001c0001t0008g0135 a0001c0002t0008g0136 others(1): Show |
4 | HG02922.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47-813A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148637874 | |||||||
chr5:148638041 | T | A | 2 | a0001c0001t0001g0258 a0001c0001t0006g0257 |
2 | HG03239.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.-47-980A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148638041 | |||||||
chr5:148638044 | G | GT | 168 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0163 others(165): Show |
171 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.-47-984dupA | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148638044 | |||||||
chr5:148638096 | G | A | 4 | a0001c0001t0008g0134 a0001c0001t0008g0135 a0001c0002t0008g0136 others(1): Show |
4 | HG02922.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47-1035C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148638096 | |||||||
chr5:148638561 | C | T | 2 | a0001c0001t0001g0208 a0001c0001t0001g0209 |
2 | NA18942.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.-47-1500G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148638561 | |||||||
chr5:148638626 | G | GAC | 4 | a0001c0001t0008g0134 a0001c0001t0008g0135 a0001c0002t0008g0136 others(1): Show |
4 | HG02922.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47-1567_-47-1566d others(4): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148638626 | |||||||
chr5:148638638 | T | G | 164 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0163 others(161): Show |
167 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.-47-1577A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148638638 | |||||||
chr5:148638647 | C | G | 6 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(3): Show |
6 | HG01884.hp1 HG02622.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.-47-1586G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148638647 | |||||||
chr5:148638760 | G | A | 4 | a0001c0001t0008g0134 a0001c0001t0008g0135 a0001c0002t0008g0136 others(1): Show |
4 | HG02922.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47-1699C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148638760 | |||||||
chr5:148638786 | A | G | 168 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0163 others(165): Show |
171 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.-47-1725T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148638786 | |||||||
chr5:148638809 | C | T | 1 | a0002c0003t0019g0123 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-47-1748G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148638809 | |||||||
chr5:148638829 | T | C | 168 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0163 others(165): Show |
171 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.-47-1768A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148638829 | |||||||
chr5:148638830 | G | A | 2 | a0001c0001t0002g0057 a0001c0001t0002g0058 |
2 | NA18941.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.-47-1769C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148638830 | |||||||
chr5:148638835 | G | A | 4 | a0001c0001t0009g0155 a0001c0001t0009g0156 a0001c0001t0009g0157 others(1): Show |
4 | HG02451.hp1 HG02559.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47-1774C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148638835 | |||||||
chr5:148638891 | C | T | 23 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0164 others(20): Show |
24 | HG01361.hp2 HG01433.hp1 HG02056.hp2 others(21): Show |
intron_variant | MODIFIER | c.-47-1830G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148638891 | |||||||
chr5:148638919 | TG | T | 23 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0164 others(20): Show |
24 | HG01361.hp2 HG01433.hp1 HG02056.hp2 others(21): Show |
intron_variant | MODIFIER | c.-47-1859delC | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148638919 | |||||||
chr5:148639122 | T | C | 1 | a0001c0001t0003g0113 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-47-2061A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148639122 | |||||||
chr5:148639264 | A | C | 4 | a0001c0001t0008g0134 a0001c0001t0008g0135 a0001c0002t0008g0136 others(1): Show |
4 | HG02922.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47-2203T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148639264 | |||||||
chr5:148639275 | C | A | 4 | a0001c0001t0008g0134 a0001c0001t0008g0135 a0001c0002t0008g0136 others(1): Show |
4 | HG02922.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47-2214G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148639275 | |||||||
chr5:148639410 | C | T | 1 | a0001c0001t0003g0121 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-47-2349G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148639410 | |||||||
chr5:148639553 | C | A | 1 | a0001c0001t0006g0200 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-47-2492G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148639553 | |||||||
chr5:148639617 | G | GTA | 22 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0001g0198 others(19): Show |
22 | HG00544.hp1 HG00673.hp2 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.-47-2558_-47-2557d others(4): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148639617 | |||||||
chr5:148639617 | G | GTATA | 27 | a0001c0001t0001g0262 a0001c0001t0001g0290 a0001c0001t0001g0291 others(24): Show |
28 | HG00738.hp1 HG01071.hp1 HG01074.hp2 others(25): Show |
intron_variant | MODIFIER | c.-47-2560_-47-2557d others(6): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148639617 | |||||||
chr5:148639617 | G | GTATATA | 64 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(61): Show |
64 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.-47-2562_-47-2557d others(8): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148639617 | |||||||
chr5:148639617 | G | GTATATAT others(1): Show |
33 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0025 others(30): Show |
33 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(30): Show |
intron_variant | MODIFIER | c.-47-2564_-47-2557d others(10): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148639617 | |||||||
chr5:148639617 | G | GTATATAT others(3): Show |
11 | a0001c0001t0002g0008 a0001c0001t0002g0072 a0001c0001t0002g0079 others(8): Show |
11 | HG00558.hp2 HG02630.hp2 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.-47-2566_-47-2557d others(12): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148639617 | |||||||
chr5:148639617 | G | GTATATAT others(5): Show |
1 | a0001c0001t0003g0095 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-47-2568_-47-2557d others(14): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148639617 | |||||||
chr5:148639617 | G | GTATATAT others(9): Show |
14 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0176 others(11): Show |
15 | HG02886.hp1 HG02895.hp2 HG03710.hp2 others(12): Show |
intron_variant | MODIFIER | c.-47-2572_-47-2557d others(18): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148639617 | |||||||
chr5:148639617 | G | GTATATAT others(11): Show |
10 | a0001c0001t0001g0161 a0001c0001t0001g0171 a0001c0001t0001g0177 others(7): Show |
10 | HG01361.hp2 HG01433.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.-47-2574_-47-2557d others(20): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148639617 | |||||||
chr5:148639617 | G | GTATATAT others(13): Show |
2 | a0001c0001t0001g0172 a0001c0001t0001g0174 |
2 | NA19065.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.-47-2576_-47-2557d others(22): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148639617 | |||||||
chr5:148639617 | G | GTATATAT others(15): Show |
4 | a0001c0001t0001g0173 a0001c0001t0001g0179 a0001c0001t0001g0180 others(1): Show |
4 | HG02056.hp2 HG02818.hp2 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47-2578_-47-2557d others(24): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148639617 | |||||||
chr5:148639617 | G | GTATATAT others(17): Show |
1 | a0001c0001t0003g0093 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-47-2580_-47-2557d others(26): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148639617 | |||||||
chr5:148639617 | GTA | G | 8 | a0001c0001t0001g0192 a0001c0001t0001g0199 a0001c0001t0001g0207 others(5): Show |
8 | HG02451.hp1 HG02559.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.-47-2558_-47-2557d others(4): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148639617 | |||||||
chr5:148639985 | C | T | 136 | a0001c0001t0001g0003 a0001c0001t0001g0185 a0001c0001t0001g0186 others(133): Show |
138 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.-47-2924G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148639985 | |||||||
chr5:148639987 | C | T | 4 | a0001c0001t0001g0264 a0001c0001t0001g0266 a0001c0001t0001g0267 others(1): Show |
4 | NA18955.hp2 NA18970.hp1 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.-47-2926G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148639987 | |||||||
chr5:148640004 | C | A | 2 | a0001c0001t0001g0198 a0001c0002t0001g0197 |
2 | HG02257.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-47-2943G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148640004 | |||||||
chr5:148640024 | C | T | 136 | a0001c0001t0001g0003 a0001c0001t0001g0185 a0001c0001t0001g0186 others(133): Show |
138 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.-47-2963G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148640024 | |||||||
chr5:148640066 | T | C | 4 | a0001c0001t0001g0003 a0001c0001t0001g0190 a0001c0001t0001g0191 others(1): Show |
5 | HG01891.hp1 HG02965.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.-47-3005A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148640066 | |||||||
chr5:148640168 | T | G | 4 | a0001c0001t0003g0090 a0001c0001t0003g0091 a0001c0001t0003g0092 others(1): Show |
4 | HG02258.hp1 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-47-3107A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148640168 | |||||||
chr5:148640210 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-47-3149C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148640210 | |||||||
chr5:148640477 | A | G | 4 | a0001c0001t0008g0134 a0001c0001t0008g0135 a0001c0002t0008g0136 others(1): Show |
4 | HG02922.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47-3416T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148640477 | |||||||
chr5:148640573 | G | A | 1 | a0001c0001t0012g0205 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-47-3512C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148640573 | |||||||
chr5:148640591 | T | G | 2 | a0001c0001t0001g0299 a0001c0001t0001g0300 |
2 | HG00741.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.-47-3530A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148640591 | |||||||
chr5:148640696 | G | C | 4 | a0001c0001t0003g0090 a0001c0001t0003g0091 a0001c0001t0003g0092 others(1): Show |
4 | HG02258.hp1 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-47-3635C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148640696 | |||||||
chr5:148641023 | C | T | 6 | a0001c0001t0002g0020 a0001c0001t0002g0021 a0001c0001t0002g0022 others(3): Show |
6 | HG01928.hp2 HG01952.hp2 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.-47-3962G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148641023 | |||||||
chr5:148641260 | T | A | 2 | a0001c0001t0001g0174 a0001c0001t0001g0180 |
2 | NA19083.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.-47-4199A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148641260 | |||||||
chr5:148641276 | A | C | 2 | a0001c0001t0001g0299 a0001c0001t0001g0300 |
2 | HG00741.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.-47-4215T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148641276 | |||||||
chr5:148641387 | T | G | 163 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0163 others(160): Show |
166 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.-47-4326A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148641387 | |||||||
chr5:148641444 | C | A | 1 | a0001c0001t0003g0116 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-47-4383G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148641444 | |||||||
chr5:148641448 | G | A | 4 | a0001c0001t0008g0134 a0001c0001t0008g0135 a0001c0002t0008g0136 others(1): Show |
4 | HG02922.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47-4387C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148641448 | |||||||
chr5:148641449 | C | A | 4 | a0001c0001t0008g0134 a0001c0001t0008g0135 a0001c0002t0008g0136 others(1): Show |
4 | HG02922.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47-4388G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148641449 | |||||||
chr5:148641450 | A | C | 4 | a0001c0001t0008g0134 a0001c0001t0008g0135 a0001c0002t0008g0136 others(1): Show |
4 | HG02922.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47-4389T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148641450 | |||||||
chr5:148641471 | C | T | 1 | a0001c0001t0009g0155 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-47-4410G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148641471 | |||||||
chr5:148641479 | T | C | 168 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0163 others(165): Show |
171 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.-47-4418A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148641479 | |||||||
chr5:148641768 | G | A | 3 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0181 |
3 | HG01361.hp2 HG01433.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.-47-4707C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148641768 | |||||||
chr5:148641806 | G | A | 1 | a0001c0001t0003g0130 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-47-4745C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148641806 | |||||||
chr5:148641949 | G | A | 6 | a0001c0001t0001g0294 a0001c0001t0001g0295 a0001c0001t0004g0293 others(3): Show |
6 | HG00544.hp1 NA18939.hp2 NA18957.hp2 others(3): Show |
intron_variant | MODIFIER | c.-47-4888C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148641949 | |||||||
chr5:148641951 | T | C | 5 | a0001c0001t0001g0183 a0001c0001t0001g0193 a0001c0001t0001g0195 others(2): Show |
5 | HG02055.hp2 HG02486.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-47-4890A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148641951 | |||||||
chr5:148642322 | T | C | 12 | a0001c0001t0001g0003 a0001c0001t0001g0190 a0001c0001t0001g0191 others(9): Show |
13 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.-47-5261A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148642322 | |||||||
chr5:148642397 | A | G | 12 | a0001c0001t0001g0003 a0001c0001t0001g0190 a0001c0001t0001g0191 others(9): Show |
13 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.-47-5336T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148642397 | |||||||
chr5:148642459 | A | G | 1 | a0001c0001t0002g0019 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-47-5398T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148642459 | |||||||
chr5:148642485 | C | A | 1 | a0001c0001t0001g0263 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-47-5424G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148642485 | |||||||
chr5:148642607 | A | G | 141 | a0001c0001t0001g0003 a0001c0001t0001g0185 a0001c0001t0001g0186 others(138): Show |
143 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.-47-5546T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148642607 | |||||||
chr5:148642621 | G | A | 23 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0164 others(20): Show |
24 | HG01361.hp2 HG01433.hp1 HG02056.hp2 others(21): Show |
intron_variant | MODIFIER | c.-47-5560C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148642621 | |||||||
chr5:148643185 | A | T | 8 | a0001c0001t0003g0090 a0001c0001t0003g0091 a0001c0001t0003g0092 others(5): Show |
8 | HG02258.hp1 HG02922.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.-47-6124T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148643185 | |||||||
chr5:148643188 | AG | A | 3 | a0001c0001t0009g0155 a0001c0001t0009g0156 a0001c0001t0009g0157 |
3 | HG02559.hp1 HG02809.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-47-6128delC | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148643188 | |||||||
chr5:148643402 | C | G | 1 | a0001c0001t0003g0087 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-47-6341G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148643402 | |||||||
chr5:148643514 | T | C | 1 | a0001c0001t0002g0076 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-47-6453A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148643514 | |||||||
chr5:148643535 | G | C | 4 | a0001c0001t0009g0155 a0001c0001t0009g0156 a0001c0001t0009g0157 others(1): Show |
4 | HG02451.hp1 HG02559.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47-6474C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148643535 | |||||||
chr5:148643563 | C | G | 8 | a0001c0001t0003g0090 a0001c0001t0003g0091 a0001c0001t0003g0092 others(5): Show |
8 | HG02258.hp1 HG02922.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.-47-6502G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148643563 | |||||||
chr5:148643715 | T | A | 1 | a0001c0001t0002g0077 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-47-6654A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148643715 | |||||||
chr5:148643789 | A | G | 1 | a0001c0001t0001g0192 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-47-6728T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148643789 | |||||||
chr5:148643823 | C | T | 1 | a0001c0001t0002g0019 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-47-6762G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148643823 | |||||||
chr5:148643990 | T | C | 1 | a0001c0001t0005g0151 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-47-6929A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148643990 | |||||||
chr5:148644009 | T | C | 8 | a0001c0001t0003g0090 a0001c0001t0003g0091 a0001c0001t0003g0092 others(5): Show |
8 | HG02258.hp1 HG02922.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.-47-6948A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148644009 | |||||||
chr5:148644024 | C | T | 5 | a0001c0001t0001g0183 a0001c0001t0001g0193 a0001c0001t0001g0195 others(2): Show |
5 | HG02055.hp2 HG02486.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-47-6963G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148644024 | |||||||
chr5:148644070 | G | T | 1 | a0001c0001t0012g0205 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-47-7009C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148644070 | |||||||
chr5:148644206 | C | T | 1 | a0001c0001t0005g0138 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-47-7145G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148644206 | |||||||
chr5:148644364 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-47-7303G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148644364 | |||||||
chr5:148644421 | AGTTTTTT others(3): Show |
A | 4 | a0001c0001t0008g0134 a0001c0001t0008g0135 a0001c0002t0008g0136 others(1): Show |
4 | HG02922.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47-7370_-47-7361d others(12): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148644421 | |||||||
chr5:148644422 | G | GT | 48 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0188 others(45): Show |
48 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(45): Show |
intron_variant | MODIFIER | c.-47-7362dupA | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148644422 | |||||||
chr5:148644422 | G | GTT | 36 | a0001c0001t0001g0185 a0001c0001t0001g0202 a0001c0001t0001g0207 others(33): Show |
36 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(33): Show |
intron_variant | MODIFIER | c.-47-7363_-47-7362d others(4): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148644422 | |||||||
chr5:148644422 | G | GTTT | 14 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0211 others(11): Show |
14 | HG02055.hp1 HG02074.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.-47-7364_-47-7362d others(5): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148644422 | |||||||
chr5:148644422 | G | GTTTTTTT others(5): Show |
1 | a0001c0001t0024g0154 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-47-7373_-47-7362d others(14): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148644422 | |||||||
chr5:148644422 | GT | G | 24 | a0001c0001t0001g0003 a0001c0001t0001g0183 a0001c0001t0001g0191 others(21): Show |
24 | HG00099.hp1 HG00140.hp2 HG00558.hp2 others(21): Show |
intron_variant | MODIFIER | c.-47-7362delA | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148644422 | |||||||
chr5:148644422 | GTT | G | 50 | a0001c0001t0002g0005 a0001c0001t0002g0013 a0001c0001t0002g0015 others(47): Show |
50 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(47): Show |
intron_variant | MODIFIER | c.-47-7363_-47-7362d others(4): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148644422 | |||||||
chr5:148644422 | GTTT | G | 39 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(36): Show |
39 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.-47-7364_-47-7362d others(5): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148644422 | |||||||
chr5:148644422 | GTTTTTTT others(3): Show |
G | 21 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0164 others(18): Show |
21 | HG01361.hp2 HG01433.hp1 HG02056.hp2 others(18): Show |
intron_variant | MODIFIER | c.-47-7371_-47-7362d others(12): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148644422 | |||||||
chr5:148644422 | GTTTTTTT others(4): Show |
G | 1 | a0001c0001t0001g0174 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-47-7372_-47-7362d others(13): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148644422 | |||||||
chr5:148644614 | A | C | 8 | a0001c0001t0003g0090 a0001c0001t0003g0091 a0001c0001t0003g0092 others(5): Show |
8 | HG02258.hp1 HG02922.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.-47-7553T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148644614 | |||||||
chr5:148644719 | G | A | 1 | a0001c0001t0003g0130 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-47-7658C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148644719 | |||||||
chr5:148644719 | G | C | 8 | a0001c0001t0003g0090 a0001c0001t0003g0091 a0001c0001t0003g0092 others(5): Show |
8 | HG02258.hp1 HG02922.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.-47-7658C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148644719 | |||||||
chr5:148644829 | C | G | 1 | a0001c0001t0003g0087 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-47-7768G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148644829 | |||||||
chr5:148644895 | G | T | 18 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0164 others(15): Show |
19 | HG02056.hp2 HG02451.hp2 HG02572.hp2 others(16): Show |
intron_variant | MODIFIER | c.-47-7834C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148644895 | |||||||
chr5:148645084 | T | C | 1 | a0001c0001t0001g0306 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-47-8023A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148645084 | |||||||
chr5:148645124 | A | G | 1 | a0001c0001t0012g0205 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-47-8063T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148645124 | |||||||
chr5:148645138 | A | G | 46 | a0001c0001t0002g0005 a0001c0001t0002g0008 a0001c0001t0003g0095 others(43): Show |
47 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.-47-8077T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148645138 | |||||||
chr5:148645259 | C | A | 1 | a0001c0001t0006g0200 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-47-8198G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148645259 | |||||||
chr5:148645369 | C | T | 1 | a0001c0002t0001g0197 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-47-8308G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148645369 | |||||||
chr5:148645389 | G | A | 8 | a0001c0001t0003g0090 a0001c0001t0003g0091 a0001c0001t0003g0092 others(5): Show |
8 | HG02258.hp1 HG02922.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.-47-8328C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148645389 | |||||||
chr5:148645507 | T | C | 128 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(125): Show |
129 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.-47-8446A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148645507 | |||||||
chr5:148645595 | C | T | 270 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0163 others(267): Show |
273 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(270): Show |
intron_variant | MODIFIER | c.-48+8467G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148645595 | |||||||
chr5:148645621 | A | G | 8 | a0001c0001t0003g0090 a0001c0001t0003g0091 a0001c0001t0003g0092 others(5): Show |
8 | HG02258.hp1 HG02922.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.-48+8441T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148645621 | |||||||
chr5:148645656 | T | C | 46 | a0001c0001t0002g0005 a0001c0001t0002g0008 a0001c0001t0003g0095 others(43): Show |
47 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.-48+8406A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148645656 | |||||||
chr5:148645812 | A | C | 1 | a0001c0001t0003g0087 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-48+8250T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148645812 | |||||||
chr5:148645857 | G | T | 4 | a0001c0001t0009g0155 a0001c0001t0009g0156 a0001c0001t0009g0157 others(1): Show |
4 | HG02451.hp1 HG02559.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.-48+8205C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148645857 | |||||||
chr5:148645904 | A | G | 133 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(130): Show |
134 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.-48+8158T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148645904 | |||||||
chr5:148645993 | G | T | 167 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0164 others(164): Show |
169 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.-48+8069C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148645993 | |||||||
chr5:148646041 | C | T | 4 | a0001c0001t0008g0134 a0001c0001t0008g0135 a0001c0002t0008g0136 others(1): Show |
4 | HG02922.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-48+8021G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148646041 | |||||||
chr5:148646115 | ACATTCAA others(16): Show |
A | 1 | a0001c0001t0014g0004 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-48+7924_-48+7946d others(25): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148646115 | |||||||
chr5:148646215 | G | C | 1 | a0001c0001t0010g0086 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-48+7847C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148646215 | |||||||
chr5:148646403 | C | T | 1 | a0001c0001t0002g0081 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-48+7659G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148646403 | |||||||
chr5:148646456 | A | G | 1 | a0001c0001t0002g0081 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-48+7606T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148646456 | |||||||
chr5:148646702 | A | G | 8 | a0001c0001t0003g0087 a0001c0001t0003g0090 a0001c0001t0003g0091 others(5): Show |
8 | HG00673.hp1 HG02258.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-48+7360T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148646702 | |||||||
chr5:148646736 | C | T | 79 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(76): Show |
79 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.-48+7326G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148646736 | |||||||
chr5:148646737 | T | C | 3 | a0001c0001t0010g0083 a0001c0001t0010g0084 a0001c0001t0017g0085 |
3 | HG02896.hp1 HG02897.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-48+7325A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148646737 | |||||||
chr5:148646747 | C | A | 2 | a0001c0001t0002g0078 a0001c0001t0002g0079 |
2 | NA18945.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.-48+7315G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148646747 | |||||||
chr5:148646776 | C | T | 3 | a0001c0001t0010g0083 a0001c0001t0010g0084 a0001c0001t0017g0085 |
3 | HG02896.hp1 HG02897.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-48+7286G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148646776 | |||||||
chr5:148646814 | A | G | 6 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(3): Show |
6 | HG01884.hp1 HG02622.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.-48+7248T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148646814 | |||||||
chr5:148646822 | A | G | 167 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0164 others(164): Show |
169 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.-48+7240T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148646822 | |||||||
chr5:148646855 | A | T | 6 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(3): Show |
6 | HG01884.hp1 HG02622.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.-48+7207T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148646855 | |||||||
chr5:148646970 | A | G | 2 | a0001c0001t0001g0198 a0001c0002t0001g0197 |
2 | HG02257.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-48+7092T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148646970 | |||||||
chr5:148647023 | C | T | 7 | a0001c0001t0003g0090 a0001c0001t0003g0091 a0001c0001t0003g0092 others(4): Show |
7 | HG02258.hp1 HG02896.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.-48+7039G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148647023 | |||||||
chr5:148647154 | C | T | 133 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0008 others(130): Show |
133 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.-48+6908G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148647154 | |||||||
chr5:148647323 | T | C | 4 | a0001c0001t0009g0155 a0001c0001t0009g0156 a0001c0001t0009g0157 others(1): Show |
4 | HG02451.hp1 HG02559.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.-48+6739A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148647323 | |||||||
chr5:148647376 | G | C | 1 | a0001c0001t0010g0086 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-48+6686C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148647376 | |||||||
chr5:148647412 | T | A | 3 | a0001c0001t0001g0299 a0001c0001t0001g0300 a0001c0001t0001g0301 |
3 | HG00738.hp2 HG00741.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.-48+6650A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148647412 | |||||||
chr5:148647526 | CA | C | 5 | a0001c0001t0001g0183 a0001c0001t0001g0193 a0001c0001t0001g0195 others(2): Show |
5 | HG02055.hp2 HG02486.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-48+6535delT | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148647526 | |||||||
chr5:148647618 | A | G | 61 | a0001c0001t0002g0005 a0001c0001t0002g0008 a0001c0001t0003g0087 others(58): Show |
61 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.-48+6444T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148647618 | |||||||
chr5:148647636 | C | G | 61 | a0001c0001t0002g0005 a0001c0001t0002g0008 a0001c0001t0003g0087 others(58): Show |
61 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.-48+6426G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148647636 | |||||||
chr5:148647639 | G | A | 15 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(12): Show |
15 | HG00673.hp1 HG01884.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.-48+6423C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148647639 | |||||||
chr5:148647650 | A | G | 4 | a0001c0001t0009g0155 a0001c0001t0009g0156 a0001c0001t0009g0157 others(1): Show |
4 | HG02451.hp1 HG02559.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.-48+6412T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148647650 | |||||||
chr5:148647674 | T | C | 59 | a0001c0001t0002g0005 a0001c0001t0002g0008 a0001c0001t0003g0087 others(56): Show |
59 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.-48+6388A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148647674 | |||||||
chr5:148647705 | T | C | 54 | a0001c0001t0002g0005 a0001c0001t0003g0087 a0001c0001t0003g0090 others(51): Show |
54 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.-48+6357A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148647705 | |||||||
chr5:148647834 | G | A | 1 | a0001c0001t0006g0200 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-48+6228C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148647834 | |||||||
chr5:148647945 | T | A | 61 | a0001c0001t0002g0005 a0001c0001t0002g0008 a0001c0001t0003g0087 others(58): Show |
61 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.-48+6117A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148647945 | |||||||
chr5:148648287 | C | G | 6 | a0001c0001t0002g0013 a0001c0001t0002g0015 a0001c0001t0002g0016 others(3): Show |
6 | HG00099.hp2 HG00323.hp1 HG00741.hp2 others(3): Show |
intron_variant | MODIFIER | c.-48+5775G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148648287 | |||||||
chr5:148648301 | G | A | 3 | a0001c0001t0010g0083 a0001c0001t0010g0084 a0001c0001t0017g0085 |
3 | HG02896.hp1 HG02897.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-48+5761C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148648301 | |||||||
chr5:148648317 | TAG | T | 4 | a0001c0001t0003g0090 a0001c0001t0003g0091 a0001c0001t0003g0092 others(1): Show |
4 | HG02258.hp1 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48+5743_-48+5744d others(4): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148648317 | |||||||
chr5:148648376 | A | G | 2 | a0001c0001t0001g0203 a0001c0001t0001g0204 |
2 | NA18967.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.-48+5686T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148648376 | |||||||
chr5:148648549 | C | T | 4 | a0001c0001t0003g0090 a0001c0001t0003g0091 a0001c0001t0003g0092 others(1): Show |
4 | HG02258.hp1 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48+5513G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148648549 | |||||||
chr5:148648573 | C | A | 74 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(71): Show |
74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.-48+5489G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148648573 | |||||||
chr5:148648640 | T | C | 1 | a0001c0001t0002g0080 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-48+5422A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148648640 | |||||||
chr5:148648645 | G | C | 1 | a0001c0001t0001g0188 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-48+5417C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148648645 | |||||||
chr5:148648698 | G | A | 1 | a0001c0001t0014g0004 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-48+5364C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148648698 | |||||||
chr5:148648816 | G | A | 76 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(73): Show |
76 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.-48+5246C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148648816 | |||||||
chr5:148648910 | A | G | 4 | a0001c0001t0009g0155 a0001c0001t0009g0156 a0001c0001t0009g0157 others(1): Show |
4 | HG02451.hp1 HG02559.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.-48+5152T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148648910 | |||||||
chr5:148648946 | G | GT | 6 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(3): Show |
6 | HG01884.hp1 HG02622.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.-48+5115dupA | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148648946 | |||||||
chr5:148649056 | G | T | 4 | a0001c0001t0003g0119 a0001c0001t0003g0132 a0001c0001t0003g0133 others(1): Show |
4 | HG01192.hp2 HG02257.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48+5006C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148649056 | |||||||
chr5:148649077 | C | T | 76 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(73): Show |
76 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.-48+4985G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148649077 | |||||||
chr5:148649200 | T | C | 76 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(73): Show |
76 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.-48+4862A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148649200 | |||||||
chr5:148649234 | C | T | 76 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(73): Show |
76 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.-48+4828G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148649234 | |||||||
chr5:148649260 | A | T | 4 | a0001c0001t0003g0119 a0001c0001t0003g0132 a0001c0001t0003g0133 others(1): Show |
4 | HG01192.hp2 HG02257.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48+4802T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148649260 | |||||||
chr5:148649273 | GAA | G | 74 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(71): Show |
74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.-48+4787_-48+4788d others(4): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148649273 | |||||||
chr5:148649424 | T | C | 4 | a0001c0001t0009g0155 a0001c0001t0009g0156 a0001c0001t0009g0157 others(1): Show |
4 | HG02451.hp1 HG02559.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.-48+4638A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148649424 | |||||||
chr5:148649534 | A | C | 76 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(73): Show |
76 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.-48+4528T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148649534 | |||||||
chr5:148649683 | A | G | 2 | a0001c0001t0003g0095 a0001c0002t0003g0094 |
2 | HG02717.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-48+4379T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148649683 | |||||||
chr5:148649734 | G | GA | 76 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(73): Show |
76 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.-48+4327dupT | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148649734 | |||||||
chr5:148649776 | G | T | 1 | a0001c0001t0001g0303 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-48+4286C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148649776 | |||||||
chr5:148649879 | G | T | 1 | a0001c0001t0001g0202 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-48+4183C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148649879 | |||||||
chr5:148650025 | T | TG | 4 | a0001c0001t0009g0155 a0001c0001t0009g0156 a0001c0001t0009g0157 others(1): Show |
4 | HG02451.hp1 HG02559.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.-48+4036dupC | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148650025 | |||||||
chr5:148650026 | G | GT | 130 | a0001c0001t0001g0192 a0001c0001t0002g0005 a0001c0001t0002g0007 others(127): Show |
130 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.-48+4035dupA | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148650026 | |||||||
chr5:148650036 | T | C | 1 | a0001c0001t0001g0302 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-48+4026A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148650036 | |||||||
chr5:148650128 | A | G | 76 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(73): Show |
76 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.-48+3934T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148650128 | |||||||
chr5:148650338 | C | T | 1 | a0001c0001t0001g0201 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-48+3724G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148650338 | |||||||
chr5:148650375 | A | G | 45 | a0001c0001t0002g0005 a0001c0001t0002g0008 a0001c0001t0003g0095 others(42): Show |
45 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.-48+3687T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148650375 | |||||||
chr5:148650501 | C | T | 182 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0163 others(179): Show |
184 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.-48+3561G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148650501 | |||||||
chr5:148650557 | T | C | 1 | a0003c0009t0027g0307 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-48+3505A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148650557 | |||||||
chr5:148650576 | A | T | 84 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0163 others(81): Show |
86 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.-48+3486T>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148650576 | |||||||
chr5:148650587 | T | C | 76 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(73): Show |
76 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.-48+3475A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148650587 | |||||||
chr5:148650614 | T | G | 1 | a0001c0001t0003g0117 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-48+3448A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148650614 | |||||||
chr5:148650723 | A | C | 76 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(73): Show |
76 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.-48+3339T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148650723 | |||||||
chr5:148650785 | G | A | 2 | a0001c0001t0003g0132 a0001c0001t0003g0133 |
2 | HG02257.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.-48+3277C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148650785 | |||||||
chr5:148650846 | A | C | 76 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(73): Show |
76 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.-48+3216T>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148650846 | |||||||
chr5:148650852 | C | T | 1 | a0001c0001t0002g0013 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-48+3210G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148650852 | |||||||
chr5:148650946 | G | C | 17 | a0001c0001t0002g0005 a0001c0001t0003g0119 a0001c0001t0003g0120 others(14): Show |
17 | HG00140.hp2 HG01192.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.-48+3116C>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148650946 | |||||||
chr5:148651031 | A | G | 76 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(73): Show |
76 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.-48+3031T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148651031 | |||||||
chr5:148651064 | T | C | 1 | a0001c0001t0001g0303 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-48+2998A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148651064 | |||||||
chr5:148651073 | C | T | 2 | a0001c0001t0002g0011 a0001c0001t0002g0012 |
2 | NA18998.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.-48+2989G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148651073 | |||||||
chr5:148651086 | TGAGAGTA others(3): Show |
T | 1 | a0001c0001t0002g0010 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-48+2966_-48+2975d others(12): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148651086 | |||||||
chr5:148651092 | T | A | 75 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0011 others(72): Show |
75 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.-48+2970A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148651092 | |||||||
chr5:148651199 | G | T | 76 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(73): Show |
76 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.-48+2863C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148651199 | |||||||
chr5:148651226 | T | C | 1 | a0001c0001t0001g0304 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-48+2836A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148651226 | |||||||
chr5:148651298 | G | A | 4 | a0001c0001t0008g0134 a0001c0001t0008g0135 a0001c0002t0008g0136 others(1): Show |
4 | HG02922.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-48+2764C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148651298 | |||||||
chr5:148651357 | G | A | 1 | a0001c0001t0005g0001 | 2 | HG01071.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.-48+2705C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148651357 | |||||||
chr5:148651398 | C | A | 76 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(73): Show |
76 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.-48+2664G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148651398 | |||||||
chr5:148651488 | C | T | 74 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(71): Show |
74 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.-48+2574G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148651488 | |||||||
chr5:148651511 | T | G | 76 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(73): Show |
76 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.-48+2551A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148651511 | |||||||
chr5:148651512 | G | A | 1 | a0001c0001t0005g0152 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-48+2550C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148651512 | |||||||
chr5:148651569 | C | T | 3 | a0001c0001t0001g0161 a0001c0002t0001g0160 a0001c0002t0001g0162 |
3 | HG02451.hp2 HG02572.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.-48+2493G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148651569 | |||||||
chr5:148651618 | A | G | 1 | a0001c0001t0002g0009 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-48+2444T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148651618 | |||||||
chr5:148651627 | T | C | 76 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(73): Show |
76 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.-48+2435A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148651627 | |||||||
chr5:148651707 | TTATTGAA others(32): Show |
T | 6 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(3): Show |
6 | HG01884.hp1 HG02622.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.-48+2316_-48+2354d others(41): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148651707 | |||||||
chr5:148651880 | C | T | 4 | a0001c0001t0003g0090 a0001c0001t0003g0091 a0001c0001t0003g0092 others(1): Show |
4 | HG02258.hp1 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48+2182G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148651880 | |||||||
chr5:148651907 | A | G | 1 | a0001c0001t0001g0183 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-48+2155T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148651907 | |||||||
chr5:148651949 | C | T | 76 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(73): Show |
76 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.-48+2113G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148651949 | |||||||
chr5:148652104 | A | G | 77 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0009 others(74): Show |
77 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.-48+1958T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148652104 | |||||||
chr5:148652377 | G | A | 4 | a0001c0001t0009g0155 a0001c0001t0009g0156 a0001c0001t0009g0157 others(1): Show |
4 | HG02451.hp1 HG02559.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.-48+1685C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148652377 | |||||||
chr5:148652393 | A | G | 76 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(73): Show |
76 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.-48+1669T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148652393 | |||||||
chr5:148652395 | C | T | 76 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(73): Show |
76 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.-48+1667G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148652395 | |||||||
chr5:148652405 | T | C | 45 | a0001c0001t0002g0005 a0001c0001t0002g0008 a0001c0001t0003g0095 others(42): Show |
45 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.-48+1657A>G | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148652405 | |||||||
chr5:148652433 | T | A | 1 | a0001c0001t0001g0181 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-48+1629A>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148652433 | |||||||
chr5:148652521 | C | T | 2 | a0001c0002t0003g0088 a0001c0002t0003g0089 |
2 | HG02145.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-48+1541G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148652521 | |||||||
chr5:148652591 | A | G | 54 | a0001c0001t0002g0005 a0001c0001t0002g0008 a0001c0001t0003g0087 others(51): Show |
54 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.-48+1471T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148652591 | |||||||
chr5:148652651 | T | G | 1 | a0001c0001t0004g0305 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-48+1411A>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148652651 | |||||||
chr5:148652669 | C | T | 1 | a0001c0001t0001g0182 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-48+1393G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148652669 | |||||||
chr5:148652728 | G | A | 4 | a0001c0001t0008g0134 a0001c0001t0008g0135 a0001c0002t0008g0136 others(1): Show |
4 | HG02922.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-48+1334C>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148652728 | |||||||
chr5:148653165 | A | G | 1 | a0001c0001t0003g0087 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-48+897T>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148653165 | |||||||
chr5:148653219 | G | T | 23 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0164 others(20): Show |
24 | HG01361.hp2 HG01433.hp1 HG02056.hp2 others(21): Show |
intron_variant | MODIFIER | c.-48+843C>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148653219 | |||||||
chr5:148653306 | C | G | 1 | a0001c0008t0001g0159 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-48+756G>C | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148653306 | |||||||
chr5:148653368 | C | T | 77 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(74): Show |
77 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.-48+694G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148653368 | |||||||
chr5:148653608 | AAC | A | 58 | a0001c0001t0001g0306 a0001c0001t0002g0005 a0001c0001t0003g0087 others(55): Show |
58 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.-48+452_-48+453del others(2): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148653608 | |||||||
chr5:148653608 | AACAC | A | 77 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(74): Show |
77 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.-48+450_-48+453del others(4): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148653608 | |||||||
chr5:148653910 | C | A | 75 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0010 others(72): Show |
75 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.-48+152G>T | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148653910 | |||||||
chr5:148653975 | C | T | 1 | a0001c0001t0004g0158 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-48+87G>A | HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 1/6 | chr5 | 148653975 |