157876713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 58457526-A-G

157877496-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58458323-A-T

157877555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58458393-G-A

157877555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58458393-G-T

157877618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58458457-T-C

http://identifiers.org/hco/2/GRCh38#157877648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58458487-C-A

157877648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58458487-C-T

http://identifiers.org/hco/2/GRCh38#157877798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58458616-C-A

157877798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58458616-C-T

157877879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58458655-G-A

157877879-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58458655-G-T

157877896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58458672-T-C

157877898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58458674-G-A

157877898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58458674-G-T

http://identifiers.org/hco/2/GRCh38#157878104-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58458850-A-C

157879524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58459624-A-G

157880252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58460065-C-T

157880431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58460242-T-C

157880485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58460315-G-A

157880834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58460596-G-A

157880892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58460656-G-A

157881151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58460913-A-G

157881370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58461106-A-G

157881370-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58461106-A-T

157882175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58462388-T-C

157882485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58462855-G-T

157882875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58463762-A-G

157882891-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58463772-C-G

157882894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58463775-C-T

http://identifiers.org/hco/2/GRCh38#157883158-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58464046-A-C

157883405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58464296-G-A

157883516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58464389-G-A

157883516-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58464389-G-C

157883516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58464389-G-T

157885121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58465003-G-A

157885269-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58465132-T-G

157885673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58465412-A-G

157885707-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58465446-T-G

157886070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58466071-C-T

157886190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58466209-G-A

157886251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58466264-T-C

157886390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58466318-C-T

http://identifiers.org/hco/2/GRCh38#157887410-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58466798-A-C

157887833-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58467483-T-A

157887875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58467525-T-C

157888048-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58467691-C-G

157888048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58467691-C-T

157888087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58467730-A-G

157890318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58468881-G-A

157890574-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58469501-A-T

157890657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58469568-A-G

157890657-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58469568-A-T

http://identifiers.org/hco/2/GRCh38#157890674-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58469595-C-A

157890674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58469595-C-T

157890845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58469798-A-G

157892053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58471907-G-A

157892547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58472759-G-T

157892580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58472792-G-A

157893015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58473231-T-C

157893568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58474556-G-A

http://identifiers.org/hco/2/GRCh38#157893672-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58474659-C-A

157893672-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58474659-C-G

157893672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58474659-C-T

157894831-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58476022-T-G

157894947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58476175-C-T

157895242-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58476479-C-G

157895398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58476635-C-T

157895801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58477008-G-A

157895891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58477063-T-C

157896376-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58477646-C-G

157896547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58478366-T-C

157896547-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58478366-T-G

157896764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58478585-C-T

157896786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58478607-C-T

157896823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58478644-G-A

157896828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58478649-G-A

157896920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58478743-A-G

157896959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58478783-C-T

157897700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58479306-G-A

157897700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58479306-G-T

157897749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58479349-G-T

157897781-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58479383-T-A

157898428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58479558-G-A

157898449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58479580-A-G

157898863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58479994-G-A

http://identifiers.org/hco/2/GRCh38#157899249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58480827-C-A

http://identifiers.org/hco/2/GRCh38#157900346-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58481566-A-C

157900479-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58481676-G-C

157900683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58481827-C-T

157900806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58482084-C-T

157901471-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58485302-T-A

157901511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58485341-A-G

157901634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58485460-T-C

157902650-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58485983-A-T

157903172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58486509-G-T

157903615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58486956-A-G

157903618-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58486959-T-G

157903861-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58487202-G-T

157904056-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58487399-G-C

157904071-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58487414-A-T

157904720-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58488110-G-C

http://identifiers.org/hco/2/GRCh38#157904806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58488185-C-A

http://identifiers.org/hco/2/GRCh38#157904816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58488195-C-A

157904816-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58488195-C-G

157904816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58488195-C-T

157904846-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58488322-T-A

157904846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58488322-T-C

157904846-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58488322-T-G

157910397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58492130-C-T

157910426-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58492150-C-G

157910426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58492150-C-T

157910559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58492291-T-C

157910573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58492305-T-C

157910574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58492306-A-G

http://identifiers.org/hco/2/GRCh38#157910575-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58492307-C-A

157910648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58492524-T-C

157910665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58492541-C-T

157910676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58492551-G-A

157910676-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58492551-G-T

157910920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58492768-C-T

157910963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58492802-T-C

157911119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58492921-A-G

157911289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58493067-G-A

157911309-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58493084-C-G

157911550-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58493314-G-C

157911550-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58493314-G-T

http://identifiers.org/hco/2/GRCh38#157911626-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58493393-A-C

157911685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58493476-C-T

157911903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58493694-C-T

157911962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58493743-A-G

http://identifiers.org/hco/2/GRCh38#157912055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58493838-C-A

157912099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58493881-T-C

157912215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58493997-T-C

157912238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58494003-G-T

157912577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58494188-G-A

157912627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58494238-T-C

157912629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58494240-G-A

157912629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58494240-G-T

157912766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58494346-T-C

157915574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58495169-C-T

157915618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58495209-C-T

157915664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58495255-G-A

157915699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58495286-T-C

157915719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58495304-G-T

157915787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58495372-C-T

157915867-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58495454-T-A

157915881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58495467-G-A

157915905-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58495480-G-C

157916077-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58495642-C-G

157916171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58495736-A-G

http://identifiers.org/hco/2/GRCh38#157916265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58495809-C-A

157916265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58495809-C-T

157916420-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58495875-G-T

157916648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58495946-G-A

157916711-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58496030-C-G

157917601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58501516-A-G

157917612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58501527-C-T

157917834-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58501714-G-T

157917835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58501715-C-T

157917884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58501754-G-A

157917886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58501756-G-A

http://identifiers.org/hco/2/GRCh38#157918038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58501896-C-A

157918062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58501920-G-A

157918096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58501956-A-G

157918119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58501978-G-A

157918125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58501984-G-T

157918184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58502030-C-T

157918424-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58502181-T-G

157918591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58502283-T-C

157918591-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58502283-T-G

157920019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58503009-G-A

157920019-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58503009-G-T

157920635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58503585-A-G

157921123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58504076-T-C

157921150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58504104-T-C

157921357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58504378-C-T

157921567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58504613-A-G

157921745-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58504739-T-A

157921839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58505342-T-C

157921870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58505369-C-T

157921953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58505443-A-G

157921964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58505454-T-C

157921984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58505474-G-A

157922172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58505615-A-G

157922270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58505709-G-T

157922309-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58505741-C-G

http://identifiers.org/hco/2/GRCh38#157922743-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58506164-C-A

157922763-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58506184-C-G

http://identifiers.org/hco/2/GRCh38#157925213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58507666-C-A

157925282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58508236-C-T

157925417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58508546-G-A

http://identifiers.org/hco/2/GRCh38#157925499-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58508625-A-C

157925654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58508789-A-G

157925668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58508803-C-T

157925696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58508822-C-T

157925764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58508881-T-C

157925837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58508951-A-G

157930642-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58510444-T-A

157930642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58510444-T-C

157930679-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58510478-G-T

157930817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58510607-C-T

http://identifiers.org/hco/2/GRCh38#157930827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58510617-C-A

157930827-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58510617-C-G

157931010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58510886-C-T

157931176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58511051-T-C

http://identifiers.org/hco/2/GRCh38#157931216-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58511090-C-A

157931257-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58511122-T-G

157931276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58511136-G-A

157931343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58511203-T-C

http://identifiers.org/hco/2/GRCh38#157931383-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58511231-A-C

http://identifiers.org/hco/2/GRCh38#157931562-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58511408-C-A

157931797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58511566-G-A

http://identifiers.org/hco/2/GRCh38#157931851-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58511620-C-A

http://identifiers.org/hco/2/GRCh38#157931855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58511624-C-A

157931855-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58511624-C-G

157932745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58516313-G-A

157932801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58516369-C-T

157932816-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58516385-T-A

157932816-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58516385-T-G

157932836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58516406-A-G

157932909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58516479-T-C

157933143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58516703-G-A

157933361-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58516890-G-C

157933445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58516969-T-C

157933446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58516970-G-A

157935250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58518294-T-C

157935314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58518342-G-A

157935379-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58518403-A-T

157935390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58518414-G-A

157935495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58518518-A-G

157935640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58518657-C-T

157936057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58519069-T-C

http://identifiers.org/hco/2/GRCh38#157936324-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58519335-A-C

157936366-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58519383-G-T

157936448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58519464-G-A

157936461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58519477-G-A

157936498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58519534-C-T

157936590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58519619-C-T

157938175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58520787-G-A

157938327-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, undefined
orthologous variants: 58520935-A-T

157938346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58520947-A-G

157938346-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58520947-A-T

157938966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58523889-G-A

157939120-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58524040-A-T

157939218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58524098-C-T

157939379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58524204-A-G

157939403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58524231-T-C

157939728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58524405-A-G

157939876-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58524536-G-C

157939968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58524626-G-T

157939970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58524628-C-T

157940144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58524787-A-G

157940221-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58524841-C-G

157940372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58524970-T-C

157940381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58524979-G-T

http://identifiers.org/hco/2/GRCh38#157940561-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58525152-A-C

157940582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58525174-T-C

157947053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58530180-G-A

157947093-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58530221-T-G

157947096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58530224-G-A

157987790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58530811-G-A

157987860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58530866-G-A

157988174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58531159-G-A

157988717-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58531650-T-A

157988726-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58531659-T-A

157988809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58531726-T-C

157988913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58531823-C-T

157989340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58532243-C-T

http://identifiers.org/hco/2/GRCh38#157989701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58532594-C-A

157989741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58532631-G-A

157989751-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58532641-C-G

157989786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58532676-C-T

http://identifiers.org/hco/2/GRCh38#157989834-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58532725-A-C

157989995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58532881-A-G

157990106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58532983-A-G

157990106-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58532983-A-T

157990141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, undefined
orthologous variants: 58533019-T-C

157990404-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58533267-G-C

157990416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58533279-C-T

157990417-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58533280-T-A

157990492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58533339-G-A

157990518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, undefined
orthologous variants: 58533381-T-C

157990677-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58533585-A-T

157990736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58533639-A-G

157990801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58533703-C-T

157990803-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58533705-T-A

157991308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58534288-C-T

157991711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58534644-A-G

157991730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58534663-G-A

157992271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58535428-G-A

157992484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58535799-G-A

http://identifiers.org/hco/2/GRCh38#157992716-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58536030-C-A

157992716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58536030-C-T

157992766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58536080-G-A

157992798-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58536112-A-T

157995017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58545222-C-T

157995037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58545241-A-G

157995039-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58545243-G-T

157995115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58545321-A-G

157995173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 58545382-T-C

157995665-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58545997-A-T

158000428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58548994-G-A

158000971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58549614-A-G

158001840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58549916-C-T

158001867-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58549941-T-G

158001909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58549983-A-G

158001951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58550025-G-A

158001951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58550025-G-T

158002429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58550477-C-T

158002484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58550525-A-G

158002502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58550543-A-G

158002562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58550571-A-G

158002570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58550579-G-A

158002750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58550761-T-C

158003215-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58551798-G-C

158003238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58551814-T-C

158003239-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58551815-G-C

158003868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58552148-G-A

158004441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58552676-C-T

http://identifiers.org/hco/2/GRCh38#158004630-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58552878-C-A

158004630-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58552878-C-G

158004630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58552878-C-T

http://identifiers.org/hco/2/GRCh38#158004690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58552938-C-A

158005020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58553254-A-G

158005339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58553909-G-A

http://identifiers.org/hco/2/GRCh38#158005961-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58554462-A-C

158006504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58554654-A-G

158006617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58554763-A-G

158006665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58554839-G-A

158007113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58555263-T-C

158007127-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58555275-T-A

158007229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58555386-T-C

158007962-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58555762-G-C

http://identifiers.org/hco/2/GRCh38#158008208-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58555985-C-A

158008208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58555985-C-T

158008230-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58556007-T-G

158008333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58556113-T-C

158008819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58556599-C-T

http://identifiers.org/hco/2/GRCh38#158009170-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58556926-C-A

158009273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58557035-G-T

158009387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58557149-G-A

158009387-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58557149-G-C

158009480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58557237-G-A

158009480-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58557237-G-C

158009511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58557268-T-C

158009514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58557271-G-A

158009649-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58557440-C-G

158009674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58557465-C-T

158009770-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58557528-T-G

158009895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58557599-T-C

158010063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58557768-T-C

158010094-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58557799-A-T

158010095-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58557800-G-T

158010147-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, undefined
orthologous variants: 58557845-C-G

http://identifiers.org/hco/2/GRCh38#158010161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#58557859-C-A

158010161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, undefined
orthologous variants: 58557859-C-T

158010217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, undefined
orthologous variants: 58557915-T-C

158010221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, undefined
orthologous variants: 58557919-G-A

158010284-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58557995-A-T

158013357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58558584-G-A

158013469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58558707-T-C

158013478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58558716-A-G

158013623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58558868-G-A

http://identifiers.org/hco/2/GRCh38#158013760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58558976-C-A

158013802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58559011-A-G

158014507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58559707-G-A

158014668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58559882-C-T

158014738-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58559955-C-G

158014795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58559989-C-T

158014796-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58559990-A-T

http://identifiers.org/hco/2/GRCh38#158016880-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58561162-A-C

158016922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58561207-T-C

http://identifiers.org/hco/2/GRCh38#158017296-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58561570-C-A

158017482-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58561747-T-A

158017649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58561903-T-C

158019621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58562288-G-A

158019621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58562288-G-T

158020171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58562774-C-T

158020434-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58562989-A-T

http://identifiers.org/hco/2/GRCh38#158020748-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58563472-A-C

158020781-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58563550-G-T

158020887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58563640-A-G

http://identifiers.org/hco/2/GRCh38#158020901-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58563654-C-A

158020901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58563654-C-T

158021034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58563898-G-A

158021053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58563917-G-T

158021075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58563939-C-T

158021204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58564056-G-A

http://identifiers.org/hco/2/GRCh38#158021377-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58568320-C-A

158021460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58568386-C-T

158021806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58568994-G-A

158021961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58569164-T-C

158022028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58569228-G-A

158022031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58569231-A-G

158022094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58569278-C-T

158023127-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58569802-T-A

158023127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58569802-T-C

158023127-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58569802-T-G

158023128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58569803-G-A

158023169-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58569831-T-A

158023248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58569897-A-G

158023249-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58569898-G-T

158023348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58569964-C-T

158023533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58570117-A-G

158023696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58570264-C-T

158023712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58570280-C-T

http://identifiers.org/hco/2/GRCh38#158024049-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58570600-A-C

158024049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58570600-A-G

158024104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58570660-G-A

158024255-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58570784-T-G

http://identifiers.org/hco/2/GRCh38#158024333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58570840-C-A

158024411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58570917-C-T

158024488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58570998-A-G

158024489-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58570999-C-G

158024846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58571345-C-T

158029318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58572612-T-C

158031089-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58586426-T-G

158031206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58586557-T-C

158031409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58586926-C-T

158031563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58587053-G-A

158031674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58587201-A-G

158031978-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58587391-T-G

158032148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58587566-G-A

158032242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58587630-A-G

158032627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58588439-A-G

158033081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58588852-A-G

158033094-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58588865-C-G

158033204-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58588986-T-G

158033229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58589010-T-C

158033253-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58589022-T-A

http://identifiers.org/hco/2/GRCh38#158033524-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58589300-C-A

158033703-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58589461-C-G

158034019-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58589784-G-C

158034218-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58589977-T-A

http://identifiers.org/hco/2/GRCh38#158034510-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58590197-C-A

158034683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58590354-A-G

158034856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58590519-G-A

158034856-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58590519-G-C

158034898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58590565-T-C

158035568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58590921-G-A

158035609-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58590948-T-A

158036738-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58591383-C-G

158036925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58591558-A-G

158037026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58591659-T-C

158037110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58591666-C-T

158037470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58591789-C-T

158037668-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58591965-G-C

158037992-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58592294-C-G

158037992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58592294-C-T

158038000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58592307-G-A

158038363-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58592641-A-T

158038411-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58592688-C-G

158038666-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58592937-T-G

158038770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58593046-T-C

158038803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58593080-G-T

158038806-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58593083-G-C

158038886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58593165-T-C

http://identifiers.org/hco/2/GRCh38#158038937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58593218-C-A

158038937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58593218-C-T

158038957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58593238-G-A

158039238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58593507-A-G

158039328-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58593586-T-G

158039536-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58593784-G-T

158039601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58593849-T-C

158039606-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58593854-C-G

158039659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58593903-T-C

158039664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58593908-T-C

158039664-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58593908-T-G

158039667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58593911-G-A

158040492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58594714-C-T

158040878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58595105-C-T

158041119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58595364-G-A

158042524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58598067-A-G

158042556-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58598100-C-G

158042556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58598100-C-T

158042631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58598175-C-T

158043213-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58598606-G-C

158043213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58598606-G-T

http://identifiers.org/hco/2/GRCh38#158043255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58598647-C-A

158043571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58598922-C-T

158043633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58599351-G-A

158043633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58599351-G-T

158043662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, undefined
orthologous variants: 58599379-G-A

158043668-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58599385-G-C

158043674-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58599391-T-G

158043916-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58599584-G-T

http://identifiers.org/hco/2/GRCh38#158044288-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58599971-C-A

158044406-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58600080-G-C

158044720-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58600354-C-G

158044823-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58600443-T-G

158044832-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58600453-T-A

158045118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58601024-C-T

158045286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58601175-A-G

158045679-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58601557-G-T

http://identifiers.org/hco/2/GRCh38#158045813-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58601677-C-A

158046303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58602147-C-T

158046476-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58602333-G-C

158046521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58602367-C-T

158046567-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58602412-T-A

158046672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58602520-C-T

158046917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58602886-G-A

158047046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58603030-G-A

158047046-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58603030-G-C

158047051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58603035-A-G

158047230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58603172-T-C

158047243-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58603184-G-C

http://identifiers.org/hco/2/GRCh38#158047298-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58603239-A-C

158047563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58603456-C-T

158047582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58603475-C-T

158048818-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58606927-A-T

158049603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58608016-G-A

158049793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58608202-C-T

158050084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58608511-A-G

158050135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58608562-A-G

158050413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58609048-C-T

158054435-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58619298-A-T

158054454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58619317-T-C

158054701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58619570-T-C

158054725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58619594-G-A

158054725-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58619594-G-C

http://identifiers.org/hco/2/GRCh38#158061140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58622412-C-A

158061145-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58622417-T-G

158061222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58622491-C-T

158061399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58622663-T-C

158061417-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58622685-T-G

158061626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58622846-C-T

158061692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58622905-T-C

158062652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58623313-C-T

158062695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58623356-C-T

158062971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58623639-A-G

158067680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58626045-C-T

http://identifiers.org/hco/2/GRCh38#158068210-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58626553-A-C

158068287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58626629-G-A

158068346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58626688-G-A

158068509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58626848-T-C

158068645-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58627006-G-C

158068754-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58627096-A-T

http://identifiers.org/hco/2/GRCh38#158069591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58627705-C-A

158069591-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58627705-C-G

158069592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58627706-C-T

158069862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58627964-T-C

158069930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58628031-G-A

158070159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58628231-C-T

http://identifiers.org/hco/2/GRCh38#158070277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58628325-C-A

158070465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58628516-G-A

158070542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58628607-T-C

158070557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58628622-C-T

158070583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58628648-T-C

158079830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58629268-T-C

158079884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, undefined
orthologous variants: 58629322-G-T

158080033-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, undefined
orthologous variants: 58629452-C-G

158080316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58629945-G-A

158080316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58629945-G-T

158080453-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58630056-A-T

158080805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58630391-A-G

158080840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58630419-G-A

158080884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58630466-G-A

158080884-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58630466-G-C

158081008-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58631722-G-C

158081077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58631795-T-C

158081248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58631967-C-T

158090654-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58632128-G-C

158090865-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58632334-G-C

158091030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58632501-G-A

158091135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58632602-T-C

158091173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58632638-A-G

http://identifiers.org/hco/2/GRCh38#158091235-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58632699-C-A

158091235-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58632699-C-G

158091239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58632703-A-G

158091406-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58632867-T-A

158091406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58632867-T-C

158093479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58636183-T-C

158093856-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58636767-G-C

158093889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58636800-C-T

158094102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58637092-C-T

158094205-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58637239-T-A

158094232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58637245-A-G

158094267-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58637292-A-T

158094369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58637397-A-G

http://identifiers.org/hco/2/GRCh38#158094656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58637771-C-A

158094686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58637801-T-C

158094957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, undefined
orthologous variants: 58638014-G-A

158094957-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, undefined
orthologous variants: 58638014-G-C

158095259-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58638284-G-C

158095490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, undefined
orthologous variants: 58638503-T-C

158095541-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58638544-C-G

158095622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58638592-C-T

158095657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58638626-G-A

158095837-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58638800-T-A

158095881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58638863-C-T

158095903-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58638885-T-G

158098548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58641499-A-G

158098586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58641537-T-C

158099052-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58642106-G-C

158099231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58642282-T-C

158099455-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58642487-G-C

158099632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58642734-C-T

158099639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58642741-G-A

158099913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58643156-G-A

158100153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58643346-G-T

158100155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58643348-A-G

158100247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58643437-A-G

158100432-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58643619-A-T

158100712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58643879-G-A

158101839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58645166-G-A

158101839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58645166-G-T

158101860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron variant
orthologous variants: 58645187-G-T

158101876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58645203-A-G

http://identifiers.org/hco/2/GRCh38#158101975-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58645301-A-C

158101975-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58645301-A-T

158101976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58645302-T-C

158102005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58645331-G-A

158102005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58645331-G-T

158102056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 58645367-T-C

158102098-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 58645407-T-A

158102098-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 58645407-T-G

158102165-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58645470-G-T

158102178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58645483-A-G

158102187-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58645492-T-A

158102187-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58645492-T-G

158102500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58646027-C-T

158102597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58646127-C-T

158102641-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58646171-C-G

158102859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58646375-G-A

158102938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58646445-C-T

158103700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58649760-G-A

158103792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58649849-C-T

158103830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58649888-A-G

158103917-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58649984-C-G

http://identifiers.org/hco/2/GRCh38#158104216-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58650477-A-C

158104307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58650563-T-C

158104408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58650663-G-A

158104579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58650804-T-C

158104607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58650832-T-C

158105057-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58650843-T-G

158105162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58650940-C-T

158105712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58653301-T-C

158106113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 58653701-A-G

158106144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 58653732-T-C

http://identifiers.org/hco/2/GRCh38#158106271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58653858-C-A

158106366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58653954-G-A

158107342-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58654979-T-A

158107497-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58655166-C-G

http://identifiers.org/hco/2/GRCh38#158107619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58655248-C-A

http://identifiers.org/hco/2/GRCh38#158107710-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58655318-A-C

158107710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58655318-A-G

158107856-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58655456-G-T

158108007-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58655593-C-G

158108234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58655864-T-C

158108312-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58655966-A-T

158108330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58655991-T-C

158108339-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58656000-C-G

158108339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58656000-C-T

158108389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58656045-T-C

158108529-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58656094-G-T

158108606-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58656166-G-C

158109261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58656822-A-G

158109426-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58657045-A-T

158109644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58657202-T-C

158109645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58657203-C-T

158112967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58658864-C-T

158113570-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58659472-G-C

158113716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58659617-A-G

158113941-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58659832-T-A

158113942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58659833-G-T

158113957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58659847-C-T

158114567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58660929-G-A

158114567-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58660929-G-T

158114646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58661010-T-C

158114853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58661199-G-T

158114988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58661317-A-G

158114988-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58661317-A-T

http://identifiers.org/hco/2/GRCh38#158115027-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58661356-A-C

158115027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58661356-A-G

http://identifiers.org/hco/2/GRCh38#158115047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58661376-C-A

158115047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58661376-C-T

158115049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58661380-G-A

158115049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58661380-G-T

158115069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58661400-T-C

158115073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58661404-G-A

158115073-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58661404-G-C

158115073-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58661404-G-T

158115117-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 58661449-G-T

http://identifiers.org/hco/2/GRCh38#158115124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58661456-C-A

158115124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 58661456-C-T

158115167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 58661499-G-A

158115167-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 58661499-G-C

158115168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 58661500-G-A

158115267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 58661599-T-C

158115273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58661606-G-T

158115320-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58661653-T-G

http://identifiers.org/hco/2/GRCh38#158115535-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58661842-C-A

http://identifiers.org/hco/2/GRCh38#158115576-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58661882-C-A

158115660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58661956-C-T

158115687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58661983-T-C

158115687-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58661983-T-G

158115768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58662058-A-G

158115964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58662223-G-A

http://identifiers.org/hco/2/GRCh38#158116251-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58662522-A-C

158116461-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58662753-T-G

158116475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58662767-C-T

158116537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58662813-T-C

158116953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58663231-G-A

158116965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58663249-G-A

158116978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58663263-T-C

158116981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58663266-T-C

158117143-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58663415-T-G

158117176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58663447-T-C

158117209-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58663484-C-G

158117209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58663484-C-T

158117211-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58663486-T-A

158117211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58663486-T-C

158117253-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58663528-T-A

http://identifiers.org/hco/2/GRCh38#158117311-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58663586-A-C

158117437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58663737-T-C

158117441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58663741-A-G

158117491-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58663807-A-T

158117546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58663862-T-C

158117555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58663871-A-G

158117617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58663926-C-T

158117700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58664009-G-T

158117721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58664030-T-C

http://identifiers.org/hco/2/GRCh38#158117818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58664122-C-A

158117818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 58664122-C-T

158117862-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 58664166-T-G

158117891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 58664195-G-A

158117891-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 58664195-G-C

158118209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58664540-G-A

158118225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58664556-G-A

158118265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58664587-G-A

158118974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58665381-G-A

158118974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58665381-G-T

158119314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58665713-A-G

158119360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58665762-G-A

158119475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58665851-A-G

158119487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58665869-C-T

158119921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58666261-G-A

http://identifiers.org/hco/2/GRCh38#158120122-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58666521-A-C

158120626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58667020-T-C

158121260-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58667661-A-T

158121270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58667671-G-T

158121284-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58667683-T-A

158121284-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58667683-T-G

158121400-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58667808-A-T

158121422-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 58667830-G-C

158121426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 58667834-G-A

158121470-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 58667878-G-C

158121494-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 58667902-C-G

158122372-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58668765-A-T

158122382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58668775-G-A

158122702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58669094-A-G

158122813-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58669206-C-G

158122813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58669206-C-T

158122894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58669290-G-A

158123146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58669478-T-C

158123309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58669643-C-T

158123475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 58669800-G-A

158123475-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 58669800-G-C

158123512-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 58669806-G-C

158123563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 58669850-G-T

158123633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58669916-A-G

158123636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58669919-A-G

158123650-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58669933-G-C

158123961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58670224-G-A

158123975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58670241-G-A

158123975-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58670241-G-T

158124003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58670269-G-A

158124006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58670272-A-G

http://identifiers.org/hco/2/GRCh38#158124821-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58670839-A-C

158124825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58670843-G-A

158124850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58670867-A-G

http://identifiers.org/hco/2/GRCh38#158125229-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58671184-A-C

158125234-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58671189-T-G

158125389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58671340-G-A

158126020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58671753-C-T

http://identifiers.org/hco/2/GRCh38#158126067-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58671801-A-C

http://identifiers.org/hco/2/GRCh38#158126115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58671843-C-A

158126204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58671936-T-C

158126314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58672033-C-T

158126332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58672097-C-T

http://identifiers.org/hco/2/GRCh38#158126333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58672098-C-A

158126333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58672098-C-T

158126342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58672107-C-T

158126363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58672132-T-C

http://identifiers.org/hco/2/GRCh38#158126369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58672138-C-A

158126408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58672185-G-A

158126408-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58672185-G-C

http://identifiers.org/hco/2/GRCh38#158126409-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58672186-C-A

158126409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58672186-C-T

158126612-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58672396-T-A

158126613-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58672397-G-C

158126635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58672417-G-A

http://identifiers.org/hco/2/GRCh38#158126650-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58672432-C-A

158126738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58672519-G-A

158126834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58672600-T-C

158126843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58672609-A-G

158126860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58672630-T-C

158126865-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58672635-G-T

158126867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58672638-T-C

158127153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58672933-C-T

158127866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58673956-G-A

158127866-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58673956-G-T

158127902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58673981-A-G

http://identifiers.org/hco/2/GRCh38#158127943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58674004-C-A

158127944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58674005-A-G

158127944-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58674005-A-T

158127979-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58674040-A-T

158128218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58674287-T-C

http://identifiers.org/hco/2/GRCh38#158128587-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#58674641-A-C

158128614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58674668-G-A

158128786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58674842-G-A

158128831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58674887-G-A

158129312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58675494-G-A

158129348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58675530-C-T

158129589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58675759-A-G

158129749-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58675916-A-T

158130157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

158130608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58676187-A-G

158130618-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58676197-T-A

158130703-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58676284-T-G

158130713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58676294-T-C

158131028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58676601-A-G

158131171-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58676749-G-C

158131171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58676749-G-T

158131260-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58676848-G-C

158131274-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58676861-C-G

158131310-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58676898-T-A

http://identifiers.org/hco/2/GRCh38#158131311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#58676899-C-A

158131326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58676914-A-G

158131698-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58677279-T-A

http://identifiers.org/hco/2/GRCh38#158131750-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58677332-C-A

158131962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58677533-C-T

158132277-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58677844-G-C

158132278-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58677845-A-T

158132280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58677847-C-T

158132314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58677866-C-T

158132472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58678002-C-T

158132606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58678131-T-C

158132607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58678132-G-A

158132865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58678244-G-A

158133194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58678616-A-G

158133248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58678660-T-C

158133351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58678761-T-C

158133360-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58678770-T-G

158133414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58678825-C-T

158133834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58679193-T-C

http://identifiers.org/hco/2/GRCh38#158133900-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58679248-C-A

158134116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58679489-T-C

158134166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58679539-T-C

http://identifiers.org/hco/2/GRCh38#158134325-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58679692-A-C

158134397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58679733-A-G

http://identifiers.org/hco/2/GRCh38#158134616-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58679921-C-A

158134616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58679921-C-T

158134628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58679933-A-G

http://identifiers.org/hco/2/GRCh38#158134711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58680004-C-A

158134724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58680017-C-T

158134729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58680022-G-A

158134729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58680022-G-T

158134732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58680025-C-T

158134782-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 58680075-C-G

158134782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 58680075-C-T

158134910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 58680203-C-T

158134916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 58680209-T-C

158134931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 58680224-T-C

158134936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 58680229-C-T

158134946-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 58680239-T-A

158134946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 58680239-T-C

158135095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 58680391-A-G

158135097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 58680393-G-A

158135097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 58680393-G-T

158135110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 58680406-G-A

158135110-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 58680406-G-C

158135110-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 58680406-G-T

http://identifiers.org/hco/2/GRCh38#158135271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58680557-C-A

158135271-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 58680557-C-G

158135521-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: 3 prime UTR variant
orthologous variants: 58680804-T-G

158135576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: 3 prime UTR variant
orthologous variants: 58680863-G-A

http://identifiers.org/hco/2/GRCh38#158135650-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58680938-C-A

158135650-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: 3 prime UTR variant
orthologous variants: 58680938-C-G

158135800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: 3 prime UTR variant
orthologous variants: 58681079-T-C

158135955-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: 3 prime UTR variant
orthologous variants: 58681234-A-T

http://identifiers.org/hco/2/GRCh38#158136025-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#58681309-C-A

158136025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23061
most severe consequence: 3 prime UTR variant
orthologous variants: 58681309-C-T