http://identifiers.org/hco/17/GRCh38#59619747-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#86648500-C-A

59619747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 86648500-C-T

59619980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 86648269-T-C

59619980-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 86648269-T-G

59620168-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, undefined
orthologous variants: 86648077-C-G

http://identifiers.org/hco/17/GRCh38#59620185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#86648060-C-A

59620185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 86648060-C-T

59620215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 86648030-G-A

59620215-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 86648030-G-T

59620409-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86647846-C-G

59620585-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86647665-C-G

http://identifiers.org/hco/17/GRCh38#59620648-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#86647602-A-C

59621035-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86647238-G-C

http://identifiers.org/hco/17/GRCh38#59621257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#86647001-C-A

59621257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86647001-C-T

59621354-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86646909-G-C

59621969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86646222-G-A

59622795-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86645745-T-A

http://identifiers.org/hco/17/GRCh38#59623136-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#86645377-A-C

59623174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86645339-G-A

59623215-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86645298-T-G

59623224-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86645289-C-G

59623454-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86645074-T-G

59623516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86645022-C-T

59623539-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86645015-A-T

59623545-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86645009-C-G

59626618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86642931-A-G

59627360-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86642595-C-G

59627360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86642595-C-T

59628370-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86640962-A-T

59628539-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86640805-G-C

59628659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86640679-G-A

59629021-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86640605-C-G

59632765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86639177-A-G

59633264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86638797-G-A

59633273-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86638783-T-G

59633807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86638213-A-G

59634632-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 86637662-A-T

59634921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86636995-C-T

http://identifiers.org/hco/17/GRCh38#59634952-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#86636960-A-C

59635354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86636558-T-C

59639997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86633026-C-T

59640000-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86633023-A-T

59640215-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86632833-C-G

59642519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86630406-G-T

59642557-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86630359-C-G

59642557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86630359-C-T

59642658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86630214-A-G

59642757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86630109-A-G

http://identifiers.org/hco/17/GRCh38#59642912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#86629980-C-A

59643298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 86629777-T-C

59643676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86628659-T-C

59643709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86628629-C-T

59643751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86628599-C-T

59643949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86628391-A-G

59644426-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 86627952-C-G

59644492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 86627886-G-A

59644492-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant, stop_gained
orthologous variants: 86627886-G-T

59645131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86627598-A-G

http://identifiers.org/hco/17/GRCh38#59645533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#86627103-C-A

59645533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86627103-C-T

http://identifiers.org/hco/17/GRCh38#59645613-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#86626939-A-C

59646114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86625918-T-C

59646514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86625510-T-C

http://identifiers.org/hco/17/GRCh38#59646574-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#86625450-A-C

59646620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86625404-T-C

59646645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86625377-G-A

59647034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86625015-C-T

59647154-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86624905-C-G

59647625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 86624441-G-A

59647699-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 86624369-G-T

http://identifiers.org/hco/17/GRCh38#59647708-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#86624360-C-A

59647889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 86624061-C-T

59647967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 86623961-A-G

59648129-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 86623602-T-A

59648129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 86623602-T-C

59648130-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 86623601-T-G

http://identifiers.org/hco/17/GRCh38#59648131-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#86623600-A-C

59648131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 86623600-A-G

59648152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 86623579-A-G

59648499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 86623248-A-G

59648525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 86623223-G-A

59648525-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 86623223-G-C

59648694-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 86623105-T-G

http://identifiers.org/hco/17/GRCh38#59648803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#86623044-C-A

59648970-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 86622836-T-A

59649156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 86622666-T-C

59649526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 86622315-A-G

http://identifiers.org/hco/17/GRCh38#59651147-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#86621712-C-A

59651147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 86621712-C-T

http://identifiers.org/hco/17/GRCh38#59651349-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#86621522-A-C

59651384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86621494-T-C

59651392-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86621486-A-T

59656022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 86621040-G-A

59656095-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 86620972-T-A

59656095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 86620972-T-C

59656095-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 86620972-T-G

59656138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 86620968-T-C

59656138-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 86620968-T-G

http://identifiers.org/hco/17/GRCh38#59656139-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#86620967-A-C

59656139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 86620967-A-G

http://identifiers.org/hco/17/GRCh38#59656143-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#86620963-C-A

59656143-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 86620963-C-G

59656143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 86620963-C-T

59656245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86618694-T-C

59656395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86618546-C-T

59656399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86618542-T-C

59656460-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86618479-T-A

http://identifiers.org/hco/17/GRCh38#59656546-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#86618395-A-C

59657431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86617564-A-G

59657441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86617554-A-G

59660262-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86617375-G-T

59660329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86617317-A-G

59660791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86616899-C-T

59660809-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86616881-A-T

59660854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86616837-T-C

59660951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86616752-G-A

59661308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86616196-C-T

59661345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86616167-A-G

59661356-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86616156-T-G

59661694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86615849-T-C

59661750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86615785-G-A

59661750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86615785-G-T

59662223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86615382-T-C

59662688-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86614933-G-C

59663683-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86613300-A-T

59663710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86613273-G-T

59663732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86613258-G-T

59663788-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86613204-T-A

59663821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86613171-A-G

59663834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 86613158-T-C

http://identifiers.org/hco/17/GRCh38#59664044-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#86612947-A-C

59664044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron variant
orthologous variants: 86612947-A-G

59664067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron variant
orthologous variants: 86612922-C-T

http://identifiers.org/hco/17/GRCh38#59664122-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#86612868-A-C

59664199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron variant
orthologous variants: 86612797-C-T

59664389-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron variant
orthologous variants: 86612711-T-G

59664627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron variant
orthologous variants: 86612664-A-G

http://identifiers.org/hco/17/GRCh38#59664639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#86612652-C-A

59664639-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron variant
orthologous variants: 86612652-C-G

59664639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron variant
orthologous variants: 86612652-C-T

59664732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 86612576-A-G

59664914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86612394-T-C

59666202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 86611112-A-G

http://identifiers.org/hco/17/GRCh38#59666295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#86610637-C-A

59666295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86610637-C-T

59666362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86610575-T-C

59666382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86610554-T-C

59666382-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86610554-T-G

59666555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 86610372-G-A

59666649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86610278-T-C

59666761-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86610207-T-G

http://identifiers.org/hco/17/GRCh38#59667153-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#86609878-A-C

59667233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron variant
orthologous variants: 86609801-G-A

59668065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron variant
orthologous variants: 86609633-C-T

59668594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron variant
orthologous variants: 86609267-G-A

59668613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron variant
orthologous variants: 86609247-T-C

59668683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron variant
orthologous variants: 86609180-G-A

http://identifiers.org/hco/17/GRCh38#59668736-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#86608931-A-C

59668997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, undefined
orthologous variants: 86608672-A-G

59669587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron variant
orthologous variants: 86607349-C-T

59670564-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron variant
orthologous variants: 86606548-A-T

59672533-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86604774-C-G

59672533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86604774-C-T

59672639-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86604647-A-T

59673287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86603928-T-C

http://identifiers.org/hco/17/GRCh38#59673502-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#86603671-A-C

59673542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86603629-T-C

59673573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86603598-A-G

59673573-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86603598-A-T

59673595-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86603581-T-G

59673834-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86603355-T-G

59674404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86603079-T-C

http://identifiers.org/hco/17/GRCh38#59674586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#86602903-C-A

59674586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86602903-C-T

59674993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86602518-T-C

59674993-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86602518-T-G

59677281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86602048-T-C

59677281-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86602048-T-G

59677624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86601803-T-C

59677696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86601725-G-A

59677783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86601631-C-T

59677786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86601628-A-G

59678210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86601056-G-A

http://identifiers.org/hco/17/GRCh38#59678216-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#86601050-C-A

59678216-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86601050-C-G

59678216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86601050-C-T

http://identifiers.org/hco/17/GRCh38#59678218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#86601039-C-A

59678218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86601039-C-T

59678246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86600958-T-C

59678319-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86600839-C-G

59678328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86600819-A-G

59678498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86600640-G-A

59678558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86600581-A-G

59679302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86599988-A-G

59679309-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86599981-T-A

59679309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86599981-T-C

http://identifiers.org/hco/17/GRCh38#59679505-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#86599788-C-A

59679505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 86599788-C-T

59679820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86599386-G-A

59679881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86599332-C-T

59680303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86598986-A-G

59680303-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86598986-A-T

59680427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86598870-C-T

59680771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86598577-A-G

59681178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86598175-A-G

http://identifiers.org/hco/17/GRCh38#59681266-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#86598084-C-A

59681434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 86597920-T-C

http://identifiers.org/hco/17/GRCh38#59681511-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#86597843-A-C

59681516-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86597809-C-G

59681516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86597809-C-T

59681557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86597771-G-A

59681557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86597771-G-T

http://identifiers.org/hco/17/GRCh38#59681577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#86597751-C-A

59681577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86597751-C-T

59681622-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86597706-C-G

59681622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86597706-C-T

59682297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 86596928-T-C

59682309-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 86596916-C-G

59682309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 86596916-C-T

59682438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86596787-C-T

http://identifiers.org/hco/17/GRCh38#59682591-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#86596171-A-C

59682591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86596171-A-G

59682591-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86596171-A-T

59682940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 86595786-C-T

59683354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86595086-C-T

59683379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 86595061-T-C

59683640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 86594811-C-T

59684005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 86594468-G-A

59684138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 86594306-T-C

59684138-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 86594306-T-G

59684140-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 86594304-T-A

59684147-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 86594298-G-C

59684147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 86594298-G-T

59684275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 86594192-A-G

59684275-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 86594192-A-T

http://identifiers.org/hco/17/GRCh38#59684984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#86593671-C-A

59684984-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86593671-C-G

http://identifiers.org/hco/17/GRCh38#59685014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#86593637-C-A

59685038-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86593612-T-A

59685038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86593612-T-C

59685342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86593386-G-A

59685342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86593386-G-T

59685348-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86593380-T-A

59685348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86593380-T-C

59685416-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86593360-A-T

http://identifiers.org/hco/17/GRCh38#59685435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#86593341-C-A

59685439-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86593337-G-C

59685439-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86593337-G-T

59685561-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86593281-T-A

59685563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86593279-G-T

59685581-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 86593260-G-C

59685581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 86593260-G-T

59685932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86592914-T-C

59686192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86592697-G-A

59686238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86592664-C-T

http://identifiers.org/hco/17/GRCh38#59686309-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#86592582-A-C

59686491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86592406-A-G

59686674-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86592237-A-T

http://identifiers.org/hco/17/GRCh38#59686855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#86592052-C-A

59687165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86591745-A-G

59687785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86591086-T-C

59688675-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86590197-C-G

59688769-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86590108-T-G

59689030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86589822-A-G

59689132-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86589724-A-T

59689178-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 86589636-T-A

http://identifiers.org/hco/17/GRCh38#59689305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#86589518-C-A

59689743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 86589041-T-C

59689756-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 86589037-G-T

59689892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 86588901-T-C

http://identifiers.org/hco/17/GRCh38#59689916-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#86588877-A-C

59690162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 86588633-A-G

http://identifiers.org/hco/17/GRCh38#59690270-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#86588528-A-C

59690270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 86588528-A-G

59690270-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 86588528-A-T

http://identifiers.org/hco/17/GRCh38#59690293-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#86588505-A-C

59690293-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 86588505-A-T

59690306-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 86588492-T-A

59690306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 86588492-T-C

59690306-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 86588492-T-G

59690429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 86588366-T-C

http://identifiers.org/hco/17/GRCh38#59690465-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#86588330-C-A

http://identifiers.org/hco/17/GRCh38#59690747-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#86588044-A-C

59691175-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86587678-C-G

59691201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86587655-A-G

59693651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86586558-G-A

59693651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86586558-G-T

59694085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 86586173-A-G

http://identifiers.org/hco/17/GRCh38#59694139-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#86586121-C-A

59694139-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 86586121-C-G

http://identifiers.org/hco/17/GRCh38#59694324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#86585937-C-A

59694324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 86585937-C-T

59694368-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 86585893-T-A

59694372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 86585889-A-G

59694515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 86585732-T-C

59694570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 86585677-A-G

59695016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 86585268-A-G

59695078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 86585209-A-G

59695268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 86585066-C-T

http://identifiers.org/hco/17/GRCh38#59695367-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#86584983-C-A

59695367-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 86584983-C-G

59695367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 86584983-C-T

59695923-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 86582668-T-G

59696312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 86582299-T-C

59696728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 86581944-G-A

59696828-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 86581855-G-C

59696828-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2092
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 86581855-G-T