43826060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77366314-G-A

43826060-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77366314-G-C

43826060-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77366314-G-T

http://identifiers.org/hco/13/GRCh38#43826239-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77366164-A-C

43826270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77366134-T-C

43826270-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77366134-T-G

43826359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77366036-C-T

43826479-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77365928-C-G

http://identifiers.org/hco/13/GRCh38#43826549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77365858-C-A

http://identifiers.org/hco/13/GRCh38#43826656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77365754-C-A

43826895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77365520-G-A

43827239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77365180-A-G

43827799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77364645-G-A

43827989-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77364455-G-T

43828026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77364418-G-A

43828026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77364418-G-T

43828265-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77363997-T-G

43828293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77363969-A-G

43828293-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77363969-A-T

43828481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77363805-A-G

http://identifiers.org/hco/13/GRCh38#43829010-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77362404-C-A

43829074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77362347-A-G

http://identifiers.org/hco/13/GRCh38#43829122-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77362297-A-C

43829241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77362165-T-C

43829639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77362114-A-G

43829676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77362070-T-C

43829720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77362051-C-T

43829800-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77361968-G-T

43830216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77361727-A-G

43830348-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77361566-G-C

43830397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77361518-C-T

43830495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77361370-A-G

43830597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77361277-G-A

43830597-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77361277-G-C

43830658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77361221-T-C

43830717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77361174-A-G

43830722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77361167-C-T

43830890-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77360988-G-C

43831210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77360668-G-A

43831315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77360601-C-T

43831343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77360572-C-T

43831383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77360534-A-G

43831383-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77360534-A-T

43831502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77360408-C-T

43831514-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77360396-T-A

43831525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77360385-T-C

43831545-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77360361-G-C

43831698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77360215-C-T

43831972-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77359939-T-A

43832061-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77359850-G-C

43832124-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77359783-T-A

43832517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77353441-A-G

43832532-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77353426-C-G

43832571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77353387-C-T

43833530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77352541-T-C

43833897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77352119-G-A

43835827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77350094-C-T

43835854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77350067-C-T

http://identifiers.org/hco/13/GRCh38#43836033-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77349892-A-C

43836054-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77349876-G-T

http://identifiers.org/hco/13/GRCh38#43836389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77349521-C-A

43836514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77349413-G-T

43836917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77349350-A-G

43836917-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77349350-A-T

http://identifiers.org/hco/13/GRCh38#43836918-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77349349-A-C

http://identifiers.org/hco/13/GRCh38#43837025-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77349255-A-C

http://identifiers.org/hco/13/GRCh38#43837067-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77349213-C-A

43837081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77349199-C-T

43837104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77349177-A-G

http://identifiers.org/hco/13/GRCh38#43837138-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77349143-A-C

43837138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77349143-A-G

http://identifiers.org/hco/13/GRCh38#43837150-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77349131-A-C

43837150-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77349131-A-T

43837182-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77349075-G-T

43837194-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77349063-T-A

43837210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77349047-G-A

43837210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77349047-G-T

43837232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77349025-G-A

43837498-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77348800-T-G

43837614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77348715-C-T

43837667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77348667-G-A

43837667-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77348667-G-C

43837685-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77348645-T-G

43837867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77348472-T-C

43837937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77348408-T-C

http://identifiers.org/hco/13/GRCh38#43837952-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77348384-C-A

43837952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77348384-C-T

43837973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77348340-G-A

43837978-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77348335-T-A

43838031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77348196-T-C

43838078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77348108-A-G

43839422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77345102-C-T

43839465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77345060-T-C

43839577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77344944-A-G

43840322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77344457-T-C

43840338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77344437-G-A

43846420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77334833-A-G

43846430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77334820-T-C

43846502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77334746-G-A

43857252-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77332044-A-T

http://identifiers.org/hco/13/GRCh38#43857344-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77331989-A-C

43857440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77331906-A-G

43858131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77331138-T-C

http://identifiers.org/hco/13/GRCh38#43858420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77330758-C-A

43858447-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77330734-G-T

43858488-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77330689-T-G

http://identifiers.org/hco/13/GRCh38#43858525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77330646-C-A

http://identifiers.org/hco/13/GRCh38#43858526-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77330645-C-A

43858526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77330645-C-T

http://identifiers.org/hco/13/GRCh38#43858543-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77330628-C-A

43858560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77330521-G-A

43858560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77330521-G-T

43858767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 77330338-T-C

43858919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77330186-A-G

43858921-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77330184-T-A

43858921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77330184-T-C

http://identifiers.org/hco/13/GRCh38#43858924-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77330181-A-C

43858924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77330181-A-G

http://identifiers.org/hco/13/GRCh38#43858926-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77330179-A-C

43858926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77330179-A-G

43858926-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77330179-A-T

43858953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77330163-T-C

43859037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77330076-T-C

43859081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77330029-C-T

43859226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77329892-C-T

43859537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77329615-T-C

43859579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77329579-T-C

43859579-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77329579-T-G

http://identifiers.org/hco/13/GRCh38#43859590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77329568-C-A

43859590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77329568-C-T

43859751-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77329425-A-T

43859752-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77329424-C-G

43859892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77329284-T-C

43859981-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 77329195-G-C

43859992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 77329184-G-A

43860054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77329122-A-G

http://identifiers.org/hco/13/GRCh38#43860079-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77329097-C-A

43860079-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77329097-C-G

43860178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77328995-T-C

43861057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77328145-G-A

43867776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77308049-A-G

43868467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77307456-T-C

43868542-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77307380-A-T

http://identifiers.org/hco/13/GRCh38#43868547-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77307375-C-A

43868547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77307375-C-T

43868550-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77307372-T-A

43868550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77307372-T-C

43868559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77307365-T-C

43868736-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 77306345-T-A

43868736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 77306345-T-C

43868758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77306323-G-A

43868758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77306323-G-T

43868772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 77306309-A-G

http://identifiers.org/hco/13/GRCh38#43868988-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77306099-C-A

43868988-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77306099-C-G

43869201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77305813-T-C

43869218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77305738-A-G

43869218-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77305738-A-T

43869275-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77305513-A-T

http://identifiers.org/hco/13/GRCh38#43869295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77305493-C-A

43869321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77305457-G-A

43869321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77305457-G-T

http://identifiers.org/hco/13/GRCh38#43869330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77305424-C-A

43869330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 77305424-C-T

43869344-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 77305399-T-A

43869344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 77305399-T-C

http://identifiers.org/hco/13/GRCh38#43869536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77305197-C-A

43869536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77305197-C-T

43869537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77305196-A-G

43869537-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77305196-A-T

43869551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77305182-G-A

43869551-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77305182-G-T

http://identifiers.org/hco/13/GRCh38#43869700-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77305052-A-C

43869755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77304935-A-G

43870349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77302817-T-C

43871339-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77301994-T-G

43871404-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77301946-A-T

43871409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77301941-C-T

43871418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77301935-T-C

43871546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77301812-C-T

43871574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77301784-T-C

43874552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77291156-C-T

43876153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77277043-C-T

http://identifiers.org/hco/13/GRCh38#43876433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77276542-C-A

43876695-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77276278-G-C

http://identifiers.org/hco/13/GRCh38#43877503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77275769-C-A

43877508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77275764-G-A

43877583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77275693-G-A

43877808-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77275478-A-T

43877862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77275424-G-T

43877926-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77275370-G-T

43877958-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77275338-G-T

43878033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77275267-T-C

http://identifiers.org/hco/13/GRCh38#43878116-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77275205-C-A

43878198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77275115-T-C

43878203-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77275110-T-A

43878513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77274887-G-A

43878513-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77274887-G-C

43878621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77274781-T-C

43878879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77274524-G-A

http://identifiers.org/hco/13/GRCh38#43878962-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77274417-C-A

43879103-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77274337-C-G

43879103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77274337-C-T

43879137-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77274297-G-T

43879174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77274264-C-T

43879187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77274251-C-T

43879220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77274213-G-A

43879220-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77274213-G-T

43879222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77274211-C-T

43879228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77274205-T-C

43879229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77274204-T-C

43879303-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77274132-C-G

43879303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26478
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77274132-C-T