113019516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 44544852-C-T

113019586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 44544785-C-T

113019652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 44544714-G-A

113019652-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 44544714-G-C

http://identifiers.org/hco/3/GRCh38#113019661-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#44544705-A-C

113019661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 44544705-A-G

113019677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 44544690-G-A

113019677-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 44544690-G-T

http://identifiers.org/hco/3/GRCh38#113019683-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#44544684-C-A

113019683-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 44544684-C-G

113019683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 44544684-C-T

http://identifiers.org/hco/3/GRCh38#113019727-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#44544665-C-A

113019727-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44544665-C-G

113019752-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44544639-G-T

113019754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44544637-G-A

113019754-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44544637-G-C

113019754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44544637-G-T

113019764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44544627-G-A

113019764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44544627-G-T

http://identifiers.org/hco/3/GRCh38#113019768-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#44544623-A-C

113019768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44544623-A-G

113019768-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44544623-A-T

http://identifiers.org/hco/3/GRCh38#113019884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#44544579-C-A

113019884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44544579-C-T

113019931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44544551-T-C

113019933-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44544549-T-A

113019933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44544549-T-C

http://identifiers.org/hco/3/GRCh38#113019977-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#44544524-A-C

113019983-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44544518-G-T

http://identifiers.org/hco/3/GRCh38#113020000-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#44544503-C-A

113020000-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44544503-C-G

113020000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44544503-C-T

113020107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44544422-G-A

113020107-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44544422-G-T

http://identifiers.org/hco/3/GRCh38#113020310-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#44544238-C-A

113020379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44544168-G-A

113020379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44544168-G-T

113020411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44544134-C-T

113020416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44544129-A-G

113020450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44544098-C-T

113020460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44544088-A-G

113020756-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44543668-G-C

113020820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44543610-G-A

113036346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44540874-G-A

113036454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44540766-T-C

113036477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44540743-C-T

113036619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44540599-A-G

113036697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44540524-A-G

113036722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44540499-C-T

113037017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44540203-T-C

113037278-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44539980-A-T

http://identifiers.org/hco/3/GRCh38#113037812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44539533-C-A

113037812-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44539533-C-G

113037855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44539497-A-G

113048855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44538280-T-C

http://identifiers.org/hco/3/GRCh38#113050942-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44538164-A-C

113051057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44538034-G-T

http://identifiers.org/hco/3/GRCh38#113051210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#44537634-C-A

113051381-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 44537454-C-G

113051381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 44537454-C-T

113051404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44537431-C-T

http://identifiers.org/hco/3/GRCh38#113051454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#44537384-C-A

113051457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 44537381-G-A

113051457-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 44537381-G-T

http://identifiers.org/hco/3/GRCh38#113051488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#44537357-C-A

113051488-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 44537357-C-G

113051488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 44537357-C-T

http://identifiers.org/hco/3/GRCh38#113051575-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#44537283-C-A

113051608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 44537256-C-T

113051614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44537248-G-T

113051648-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 44537204-G-T

113052072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44536776-A-G

113052248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44536635-T-C

113052615-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44529851-G-T

113052661-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44529805-A-T

113052962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44529289-T-C

113053126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44529133-T-C

113053266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44529012-T-C

113053267-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44529011-G-C

113053267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44529011-G-T

113053282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44528997-C-T

113053392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44527925-G-A

113053571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44527749-T-C

113053617-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44527701-G-C

113053617-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44527701-G-T

113053725-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44527642-T-A

113054145-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44526926-T-G

113054155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44526916-T-C

113054279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44526805-C-T

113054355-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44526763-G-C

113054621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44526507-A-G

113054695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44526429-A-G

113054840-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44526305-G-C

113054844-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44526301-C-G

113055355-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44525868-A-T

113055482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44525766-A-G

113055863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44525421-A-G

113055906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44525379-A-G

113055984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44525304-T-C

113056160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44525154-G-A

113056426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44524895-G-A

113056486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44524833-C-T

113056488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44524831-T-C

http://identifiers.org/hco/3/GRCh38#113056526-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44524793-C-A

113056526-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44524793-C-G

113056526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44524793-C-T

113056597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44524728-G-A

113056602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44524723-C-T

113056654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44524660-G-A

113056654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44524660-G-T

113056756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44524547-T-C

113056775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44524528-T-C

113056825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44524421-C-T

113056896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44524346-G-A

113057132-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44524159-T-G

113057223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44524074-A-G

113057313-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44523987-G-C

113057393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44523915-T-C

113057688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44523609-C-T

113057696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44523603-A-G

113057713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44523586-T-C

113062935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44520648-C-T

113062969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44520615-T-C

113062989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44520595-A-G

113063119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44520457-G-A

113063119-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44520457-G-T

113063153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44520423-C-T

113063340-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44519054-A-T

113063349-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44519043-T-G

113063408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44518989-G-A

113063408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44518989-G-T

113063412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44518985-G-A

113063412-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44518985-G-C

113063412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44518985-G-T

http://identifiers.org/hco/3/GRCh38#113063430-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44518967-A-C

113063477-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44518892-G-C

113064267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44518183-C-T

113064542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44517904-T-C

113069529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44517083-G-A

113069873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44516777-C-T

113069932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44516738-T-C

113070871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44515954-C-T

113070888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44515934-T-C

113071107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44515718-C-T

113071145-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44515690-A-T

113071148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44515687-A-G

http://identifiers.org/hco/3/GRCh38#113071169-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44515643-A-C

113071169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44515643-A-G

113079228-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44512852-A-T

113079442-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44512349-T-G

113079626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44512174-C-T

113079753-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44512045-A-T

113079778-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44512020-C-G

113079912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44511887-G-A

113079912-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44511887-G-C

http://identifiers.org/hco/3/GRCh38#113079937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44511861-C-A

113080139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44511476-G-A

113081036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44510501-T-C

113084458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44509619-G-A

113084813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44509308-G-T

113086143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44508598-G-T

113086329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44508358-T-C

113086386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44508275-C-T

113086430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44508218-G-A

113086616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44508026-G-A

113086919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44507723-G-A

113087001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44507642-G-A

113087001-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44507642-G-T

113087133-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44507479-C-G

113087229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44507386-C-T

113087509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44506798-G-A

113087513-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44506794-A-T

113087538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44506769-A-G

113087619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44506692-A-G

http://identifiers.org/hco/3/GRCh38#113087742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44506567-C-A

113087754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44506555-C-T

113087903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44506425-T-C

113087957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44506381-T-C

http://identifiers.org/hco/3/GRCh38#113087975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44506368-C-A

113088242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44506100-A-G

113088299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44506057-G-A

113088415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44505941-G-A

http://identifiers.org/hco/3/GRCh38#113088499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44505858-C-A

http://identifiers.org/hco/3/GRCh38#113088502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44505855-C-A

113088502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44505855-C-T

113088530-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44505827-T-A

113088530-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44505827-T-G

113088556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44505798-G-A

113088576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44505778-A-G

113088612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44505737-T-C

113088616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 44505733-T-C

113088679-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44505672-G-C

113088679-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44505672-G-T

http://identifiers.org/hco/3/GRCh38#113088776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44505579-C-A

113088776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44505579-C-T

113088783-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44505572-A-T

113088887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44505464-C-T

http://identifiers.org/hco/3/GRCh38#113088945-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44505404-C-A

http://identifiers.org/hco/3/GRCh38#113088997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44505358-C-A

113088997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44505358-C-T

113089005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44505350-C-T

113089124-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44505336-T-A

113089124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44505336-T-C

113089891-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44504665-G-C

113089891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44504665-G-T

113089896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44504660-T-C

113089936-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44504478-T-G

113089983-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44504430-G-T

113090264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44504202-G-A

113090277-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44504189-C-G

113090457-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44503830-A-T

113090802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44503467-T-C

113090843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44503426-A-G

113092649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44501657-A-G

113092685-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44501621-G-C

113092726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44501584-T-C

113092786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44501538-G-A

http://identifiers.org/hco/3/GRCh38#113092822-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44501514-C-A

http://identifiers.org/hco/3/GRCh38#113093609-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44501063-C-A

113093609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44501063-C-T

113093667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44501019-G-T

113093734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44500960-A-G

113093846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44500860-A-G

113094571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44500159-G-A

113094571-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44500159-G-C

113094571-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44500159-G-T

113094586-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44500144-G-C

113094997-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44499691-C-G

113095204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44499477-G-A

113095328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44499362-A-G

113095495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44499195-A-G

http://identifiers.org/hco/3/GRCh38#113095718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44498938-C-A

113095845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44498824-A-G

113095859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44498810-C-T

113096078-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44498562-A-T

113096223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44498435-C-T

113096269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44498389-T-C

113096624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44498021-G-T

113096813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44497834-T-C

113096876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44497795-A-G

113097725-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44496912-T-G

113097921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44496470-G-A

113097980-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44496417-G-T

113098216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44496199-G-T

113098450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44495973-T-C

113102340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44495029-T-C

http://identifiers.org/hco/3/GRCh38#113102659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44494733-C-A

113102659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44494733-C-T

113102770-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44494636-C-G

113103067-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44494340-A-T

113103136-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44494268-T-A

http://identifiers.org/hco/3/GRCh38#113103144-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44494261-C-A

113103188-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44494217-G-C

http://identifiers.org/hco/3/GRCh38#113103304-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44494105-C-A

113103383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44494025-T-C

113103388-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44494021-G-C

113103963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44493486-G-A

113104314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44493083-T-C

113104416-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44493015-C-G

113104416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44493015-C-T

http://identifiers.org/hco/3/GRCh38#113104459-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44492969-A-C

113104459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44492969-A-G

113104459-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44492969-A-T

113104469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44492959-G-A

113104469-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44492959-G-T

113104475-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44492953-G-T

113104479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44492949-G-A

113104825-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44492595-G-C

http://identifiers.org/hco/3/GRCh38#113104881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44492539-C-A

113104881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44492539-C-T

113104892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44492528-C-T

113105020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44492390-C-T

113105073-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44492337-G-T

113105392-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44491997-A-T

113105860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44491587-C-T

113106015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44491435-C-T

113106215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44490937-G-A

http://identifiers.org/hco/3/GRCh38#113106249-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44490903-A-C

113106298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44490854-T-C

113106333-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44490819-T-G

113106384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44490781-C-T

113106839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44490309-G-A

113106875-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44490273-C-G

113106875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44490273-C-T

113107097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44490059-A-G

http://identifiers.org/hco/3/GRCh38#113107101-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44490055-A-C

113107179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44489977-A-G

113107203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44489953-G-T

113107394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44489792-C-T

113107569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44489636-A-G

113107786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44489330-G-A

113108206-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44488782-G-T

113108349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44488665-T-C

113108464-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44488551-T-G

113108777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44488279-C-T

113108976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44488062-T-C

113109028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44488020-A-G

113109595-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44487508-T-G

113109699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44487422-C-T

113109972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44487142-G-T

113110493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44486954-G-T

113110704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44486750-C-T

113110713-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44486741-G-C

113110857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44486619-G-A

113110858-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44486618-G-T

113110983-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44486528-C-G

113111016-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44486494-T-G

113111030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44486463-A-G

113111087-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44486404-G-C

113111202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44486311-G-A

113112434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44485571-T-C

113112493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44485513-A-G

113120597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44484660-A-G

113120982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44484292-C-T

113121178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44484101-G-A

113121178-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44484101-G-T

113121230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44484074-A-G

113121357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44483951-A-G

113121391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44483917-G-A

113121417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44483891-G-A

113121793-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44483475-A-T

113121904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44483379-C-T

113122235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44483084-G-A

113122727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44482846-G-A

113122768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44482782-T-C

113122875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44482687-T-C

113123035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44482644-C-T

113123179-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44482488-G-T

http://identifiers.org/hco/3/GRCh38#113123185-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44482482-A-C

113123185-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44482482-A-T

113123580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44482422-T-C

113123697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44482325-C-T

http://identifiers.org/hco/3/GRCh38#113123797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44482271-C-A

113123797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44482271-C-T

113123908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44482201-G-A

113123908-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44482201-G-C

113123908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44482201-G-T

113124009-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44482100-T-G

113124061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44481943-T-C

113124362-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44481659-G-C

113124404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44481614-G-A

113124529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44481495-T-C

113124631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44481437-G-A

113124632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44481436-C-T

113125198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44480582-A-G

113125217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44480563-G-A

113125549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44478845-G-A

113125949-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44478257-G-C

113126085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44478056-C-T

113126105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44477994-A-G

113126122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44477977-G-A

113126206-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44477903-C-G

113126241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44477868-C-T

113126419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44477740-A-G

113126767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44477420-G-A

113126770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44477417-C-T

113128352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44476271-A-G

113128390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44476239-G-A

113128408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44476223-C-T

113128422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44476208-T-C

113128475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44476187-C-T

113128533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44476128-T-C

113128603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44476051-T-C

113128724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44475924-A-G

http://identifiers.org/hco/3/GRCh38#113128853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44475788-C-A

113128853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44475788-C-T

113129010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44475631-T-C

113129395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44475048-G-A

113129398-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44475045-A-T

113129529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44474925-T-C

113130281-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44474062-G-C

113131378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44471588-A-G

113131544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44471423-G-A

113131825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44471142-G-A

113131908-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44471058-T-G

113132648-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44469756-C-G

113132743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44469660-C-T

113133006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44469393-C-T

113133106-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44469310-G-C

113136112-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44464647-C-G

113136426-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44464320-T-G

113136669-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44463806-A-T

113138943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44459138-T-C

113138998-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44459089-T-G

113139212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44458870-C-T

113139303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44458776-C-T

113139678-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44457964-A-T

113139801-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44457852-G-C

http://identifiers.org/hco/3/GRCh38#113143334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44456748-C-A

113143404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44456676-G-T

113143700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44456384-G-T

http://identifiers.org/hco/3/GRCh38#113143705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44456380-C-A

113143705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44456380-C-T

http://identifiers.org/hco/3/GRCh38#113143707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44456378-C-A

113143707-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44456378-C-G

113143725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44456360-C-T

http://identifiers.org/hco/3/GRCh38#113143727-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44456358-C-A

http://identifiers.org/hco/3/GRCh38#113143822-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44456219-A-C

113143822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44456219-A-G

113143838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44456203-A-G

113143865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44456175-A-G

http://identifiers.org/hco/3/GRCh38#113143894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44456122-C-A

113143988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44455869-G-A

113144100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44455779-T-C

113144120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44455759-A-G

113144244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44455666-G-A

113144591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44455354-T-C

113147978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44453424-T-C

113147979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44453423-C-T

113148162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44453243-A-G

113148400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44453002-C-T

113148401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44453001-C-T

113148550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44452850-C-T

113148823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44452618-A-G

113148838-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44452603-C-G

http://identifiers.org/hco/3/GRCh38#113148941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44452477-C-A

113148941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44452477-C-T

http://identifiers.org/hco/3/GRCh38#113149061-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44452395-A-C

113149168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44452305-C-T

113149169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44452304-C-T

113150023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44452037-C-T

113150090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44451975-C-T

113150133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44451963-G-A

113150141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44451955-T-C

113150256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44451866-G-A

113150256-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44451866-G-C

113150481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44451665-C-T

113150561-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44451599-G-C

113150637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44451523-T-C

113150637-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44451523-T-G

113150678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44451483-T-C

113150991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44451138-C-T

113151276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44450897-A-G

113151732-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44450429-T-A

113151732-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44450429-T-G

113153738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44449873-C-T

113153857-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44449785-C-G

113154001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44449641-C-T

113154890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44448008-T-C

113154942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44447957-T-C

113155013-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44447885-A-T

http://identifiers.org/hco/3/GRCh38#113156538-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44447494-C-A

113156642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44447411-A-G

http://identifiers.org/hco/3/GRCh38#113156870-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44447240-A-C

http://identifiers.org/hco/3/GRCh38#113156993-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44447136-C-A

113156993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44447136-C-T

113157200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44446927-G-A

113157296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44446843-C-T

113157468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44446675-T-C

http://identifiers.org/hco/3/GRCh38#113157669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44446488-C-A

113157898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44446250-A-G

113157908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44446240-G-T

http://identifiers.org/hco/3/GRCh38#113157911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44446237-C-A

113157981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44446210-G-A

113158073-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44446168-G-T

113158074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44446167-A-G

113158074-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44446167-A-T

113158076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44446165-G-A

113158076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44446165-G-T

113158137-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44446122-G-T

http://identifiers.org/hco/3/GRCh38#113158384-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44445914-C-A

113158384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44445914-C-T

113158425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44445872-G-A

113158425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44445872-G-T

113158426-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44445871-C-G

113158426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44445871-C-T

http://identifiers.org/hco/3/GRCh38#113158466-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44445840-C-A

http://identifiers.org/hco/3/GRCh38#113158546-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44445783-C-A

113158597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44445734-A-G

http://identifiers.org/hco/3/GRCh38#113158735-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44445530-C-A

113159010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44444605-G-A

http://identifiers.org/hco/3/GRCh38#113159022-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44444593-A-C

113159022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44444593-A-G

113159246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44444371-T-C

113159269-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44444348-G-T

113159365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44444203-C-T

113159378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44444190-T-C

http://identifiers.org/hco/3/GRCh38#113159383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44444185-C-A

113159383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44444185-C-T

113160885-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44443423-T-G

113161009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44443297-T-C

113161262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44442906-C-T

http://identifiers.org/hco/3/GRCh38#113162315-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44441827-A-C

113162835-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44441340-T-A

113162835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44441340-T-C

113162901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44441275-G-A

113163115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44441057-G-A

113163281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44440599-C-T

113163294-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44440588-T-G

113163391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44440483-C-T

113163488-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44440388-A-T

http://identifiers.org/hco/3/GRCh38#113163727-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44440162-C-A

113163741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44440148-C-T

http://identifiers.org/hco/3/GRCh38#113163748-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44440141-C-A

113163748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44440141-C-T

113163752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44440137-A-G

113163842-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44440038-A-T

113164830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44439711-A-G

113164856-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44439677-T-A

113164875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44439658-A-G

113164999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44439334-T-C

113165138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44439198-C-T

113165142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44439194-A-G

http://identifiers.org/hco/3/GRCh38#113165169-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44439164-C-A

http://identifiers.org/hco/3/GRCh38#113165180-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44439153-C-A

113165180-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44439153-C-G

http://identifiers.org/hco/3/GRCh38#113165231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44439106-C-A

113165231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44439106-C-T

113165266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44439059-G-A

113165310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44439004-A-G

113165360-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44438314-G-C

113165617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44438113-A-G

113165712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44438030-A-G

113166196-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44437567-G-T

113166541-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44437230-C-G

http://identifiers.org/hco/3/GRCh38#113167061-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#44436691-C-A

113167684-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44436068-G-T

113167744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44436029-G-A

http://identifiers.org/hco/3/GRCh38#113167801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44435951-C-A

113167833-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44435919-T-G

http://identifiers.org/hco/3/GRCh38#113168130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44435621-C-A

113168752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44434656-G-A

113168767-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44434641-G-T

113168820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44434588-G-A

113168883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44434521-G-T

113168929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44434482-C-T

http://identifiers.org/hco/3/GRCh38#113169363-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44434053-C-A

http://identifiers.org/hco/3/GRCh38#113169530-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44433855-C-A

113169863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44433587-A-G

113169912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44433544-A-G

113169916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44433540-G-A

113169922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44433535-T-C

113170558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44432958-C-T

113171036-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44432014-G-C

113172759-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44431849-T-A

113173039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44430707-G-A

113173345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44429849-G-A

113173352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44429842-A-G

113173376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44429818-A-G

113173591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44429659-G-A

113173591-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44429659-G-C

113173591-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44429659-G-T

113173641-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44429611-T-A

113173641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44429611-T-C

113173805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44429423-A-G

113174274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44429268-G-T

113174308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44429235-T-C

113174346-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44427522-T-G

113174350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44427518-G-A

113174568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44427322-T-C

113174606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44427281-G-A

http://identifiers.org/hco/3/GRCh38#113174832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44424981-C-A

113174832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44424981-C-T

113174833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44424980-G-A

113175075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44424768-A-G

113175085-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44424760-C-G

113175128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44424734-G-A

113175296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44424567-G-A

113175476-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44424338-T-A

113175714-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44424097-G-T

113175857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44423970-A-G

113175862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44423965-C-T

113178619-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44423689-C-G

113178744-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44423564-G-T

113178778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44423530-G-A

113178875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44423439-C-T

113179703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44422831-A-G

113180337-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44422001-G-C

113180477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44421846-C-T

113180489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44421836-C-T

http://identifiers.org/hco/3/GRCh38#113180600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44421718-C-A

113180679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44421636-G-A

113180754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44421559-T-C

http://identifiers.org/hco/3/GRCh38#113180777-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44421536-C-A

113180779-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44421534-C-G

113180779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44421534-C-T

113180810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44421503-A-G

113180886-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44421438-A-G

http://identifiers.org/hco/3/GRCh38#113181203-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44421173-A-C

113181374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44420996-A-G

113181374-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44420996-A-T

113182036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44420135-G-A

113182113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44420035-T-C

113182177-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44419977-C-G

http://identifiers.org/hco/3/GRCh38#113182240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44419921-C-A

113182311-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44419848-G-T

113182341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44419820-T-C

113184162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: non coding transcript exon variant
orthologous variants: 44417994-C-T

113184226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: non coding transcript exon variant
orthologous variants: 44417944-A-G

113184279-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41049
most severe consequence: non coding transcript exon variant
orthologous variants: 44417888-C-G