http://identifiers.org/hco/17/GRCh38#76389514-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116428557-A-C

http://identifiers.org/hco/17/GRCh38#76389688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116428685-C-A

76389688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: 3 prime UTR variant
orthologous variants: 116428685-C-T

76389740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: 3 prime UTR variant
orthologous variants: 116428724-A-G

76389981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: 3 prime UTR variant
orthologous variants: 116428986-G-A

76389981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: 3 prime UTR variant
orthologous variants: 116428986-G-T

76389988-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: 3 prime UTR variant
orthologous variants: 116428993-A-T

76390062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: 3 prime UTR variant
orthologous variants: 116429084-T-C

http://identifiers.org/hco/17/GRCh38#76390148-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116429172-C-A

http://identifiers.org/hco/17/GRCh38#76390183-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116429206-C-A

76390183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: 3 prime UTR variant
orthologous variants: 116429206-C-T

76390264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: 3 prime UTR variant
orthologous variants: 116429279-T-C

76390388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: 3 prime UTR variant
orthologous variants: 116429370-T-C

76390388-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: 3 prime UTR variant
orthologous variants: 116429370-T-G

http://identifiers.org/hco/17/GRCh38#76390411-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116429393-C-A

76390411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: 3 prime UTR variant
orthologous variants: 116429393-C-T

76390481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: 3 prime UTR variant
orthologous variants: 116429449-A-G

76390495-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: 3 prime UTR variant
orthologous variants: 116429463-G-T

76390699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: 3 prime UTR variant
orthologous variants: 116429633-G-A

76390699-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: 3 prime UTR variant
orthologous variants: 116429633-G-C

76390699-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: 3 prime UTR variant
orthologous variants: 116429633-G-T

http://identifiers.org/hco/17/GRCh38#76390792-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116429714-C-A

76390792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: 3 prime UTR variant
orthologous variants: 116429714-C-T

76390802-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: 3 prime UTR variant
orthologous variants: 116429724-T-A

76390841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: 3 prime UTR variant
orthologous variants: 116429766-G-A

76390841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: 3 prime UTR variant
orthologous variants: 116429766-G-T

http://identifiers.org/hco/17/GRCh38#76390936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116429862-C-A

76390936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: 3 prime UTR variant
orthologous variants: 116429862-C-T

76390964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: synonymous variant
orthologous variants: 116429891-C-T

76391279-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: synonymous variant
orthologous variants: 116430203-G-C

76391453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: synonymous variant
orthologous variants: 116430377-A-G

76391678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron variant
orthologous variants: 116430587-C-T

76391720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron variant
orthologous variants: 116430606-T-C

76391720-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron variant
orthologous variants: 116430606-T-G

76391730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron variant
orthologous variants: 116430616-G-A

76391730-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron variant
orthologous variants: 116430616-G-T

76391967-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: synonymous variant
orthologous variants: 116430815-G-C

76392136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron variant
orthologous variants: 116430982-A-G

76392136-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron variant
orthologous variants: 116430982-A-T

76392215-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron variant
orthologous variants: 116431027-T-G

76395904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116432085-C-T

76396012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116432116-G-A

76396038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116432141-G-A

76396038-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116432141-G-T

76396042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116432145-T-C

http://identifiers.org/hco/17/GRCh38#76396108-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116432147-C-A

76396108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116432147-C-T

76396245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116432282-C-T

76396267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116432304-G-A

76396267-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116432304-G-C

76396381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116432418-C-T

76396522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116432559-G-A

76396665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116432708-G-A

76396708-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116432751-C-G

76396708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116432751-C-T

76396825-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 116432868-G-C

76396970-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116432955-T-A

76396970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116432955-T-C

76396970-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116432955-T-G

76397020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116433005-G-A

76397312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116433308-T-C

76397331-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116433327-G-C

76397471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116433445-G-A

76397736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116433586-G-A

76397736-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116433586-G-T

76397891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, stop_gained
orthologous variants: 116433709-G-A

http://identifiers.org/hco/17/GRCh38#76398117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116434049-C-A

76398235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116434207-A-G

76398267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116434246-G-A

76398285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116434264-A-G

76398297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116434276-G-A

http://identifiers.org/hco/17/GRCh38#76398327-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#116434306-A-C

76398327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 116434306-A-G

76398327-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 116434306-A-T

http://identifiers.org/hco/17/GRCh38#76398420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116434398-C-A

76398453-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116434429-C-G

76398458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116434434-G-A

76398597-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116434571-A-T

76398904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116434759-G-A

76398907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116434762-G-A

76399046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116434900-G-A

76399046-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116434900-G-T

76399126-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116434956-T-A

76399126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116434956-T-C

http://identifiers.org/hco/17/GRCh38#76399127-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116434957-C-A

http://identifiers.org/hco/17/GRCh38#76399238-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116435031-C-A

76399238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116435031-C-T

http://identifiers.org/hco/17/GRCh38#76399294-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116435060-C-A

76399294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116435060-C-T

76399374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116435137-C-T

76399526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116435251-G-A

76399526-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116435251-G-C

76399658-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116435383-C-G

76399658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116435383-C-T

76399664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116435389-G-A

76399664-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116435389-G-C

76399730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116435455-A-G

76399808-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116435533-G-C

http://identifiers.org/hco/17/GRCh38#76399972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116435702-C-A

76399972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116435702-C-T

76400346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116436065-C-T

76400380-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116436096-C-G

76400380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116436096-C-T

76400407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116436113-G-A

76400434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 116436140-T-C

76400556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 116436266-G-A

76400556-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 116436266-G-T

http://identifiers.org/hco/17/GRCh38#76400636-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116436322-C-A

76400667-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116436384-A-T

http://identifiers.org/hco/17/GRCh38#76400684-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116436401-C-A

76400684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116436401-C-T

76400690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116436407-A-G

76400690-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116436407-A-T

76400701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116436420-G-A

76400701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116436420-G-T

76400800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116436497-C-T

76400852-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116436544-C-G

76400893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116436585-G-A

76400893-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116436585-G-C

76400893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116436585-G-T

http://identifiers.org/hco/17/GRCh38#76401002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116436651-C-A

76401002-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116436651-C-G

76401002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116436651-C-T

76401065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116436714-T-C

76401134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116436783-G-A

76401134-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116436783-G-C

http://identifiers.org/hco/17/GRCh38#76401171-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116436820-C-A

76401769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116436969-G-A

76401769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116436969-G-T

http://identifiers.org/hco/17/GRCh38#76401845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116437034-C-A

76401845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116437034-C-T

http://identifiers.org/hco/17/GRCh38#76401857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116437048-C-A

76401866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116437057-T-C

http://identifiers.org/hco/17/GRCh38#76401873-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116437064-C-A

76401873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116437064-C-T

76401916-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116437157-T-A

76401916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116437157-T-C

76401971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116437209-C-T

76402158-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116437381-C-G

http://identifiers.org/hco/17/GRCh38#76402178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116437399-C-A

http://identifiers.org/hco/17/GRCh38#76402247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116437447-C-A

http://identifiers.org/hco/17/GRCh38#76402492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116437615-C-A

76402505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116437628-T-C

76402573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116437686-C-T

76402770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116437856-A-G

76404993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116439426-T-C

http://identifiers.org/hco/17/GRCh38#76405043-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116439475-A-C

76405106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116439546-G-A

76405106-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116439546-G-C

76405106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116439546-G-T

76405113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116439553-G-A

76405113-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116439553-G-T

76405145-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116439580-T-G

76405260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116439650-G-A

http://identifiers.org/hco/17/GRCh38#76405433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116439805-C-A

76405646-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116439962-G-T

76406079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116440251-A-G

76406453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116440538-C-T

http://identifiers.org/hco/17/GRCh38#76406474-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116440563-C-A

76406572-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116440657-T-A

76410901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116443013-C-T

76410927-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116443039-C-G

76411532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116443367-T-C

76411661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116443464-G-A

76411667-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116443470-T-G

76416572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116443987-G-A

76417192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116444568-C-T

76417511-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116444869-C-G

http://identifiers.org/hco/17/GRCh38#76417758-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116445111-A-C

http://identifiers.org/hco/17/GRCh38#76418928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116446128-C-A

76418928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116446128-C-T

76418930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116446130-C-T

76420021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116446859-G-A

76420610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116447334-T-C

76420652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116447344-G-A

76420660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116447349-T-C

76421817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116448721-C-T

76421947-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116448842-G-C

76422004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116448885-T-C

http://identifiers.org/hco/17/GRCh38#76422378-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116449137-A-C

76423158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116449771-G-T

76435738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116455815-G-A

76435959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116456012-T-C

76438606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116458128-T-C

76438819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116458284-G-A

76440933-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116460683-G-C

76441138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116460869-G-A

76441271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116460972-T-C

76441576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116461212-T-C

76441611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116461248-G-A

76441611-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116461248-G-C

76441746-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116461368-T-A

76442048-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116461589-C-G

76442048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116461589-C-T

76443927-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116463310-G-C

76444668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116463652-G-A

76444854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116463819-T-C

76444871-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116463836-A-T

76445111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116464025-T-C

76445146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116464061-G-A

76445217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116464126-G-A

76445240-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116464144-A-T

76445270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116464169-T-C

76445271-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116464177-A-T

76445283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116464189-C-T

76445575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116464516-T-C

76445604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116464549-G-A

76446080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116464995-T-C

76446657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116465475-C-T

76446684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116465486-G-A

http://identifiers.org/hco/17/GRCh38#76446730-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116465528-A-C

76446825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116465585-T-C

76446857-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116465615-T-G

76447623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116466091-G-A

http://identifiers.org/hco/17/GRCh38#76447698-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116466157-A-C

http://identifiers.org/hco/17/GRCh38#76447726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116466188-C-A

76447824-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116466249-A-T

76448145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116466524-G-A

76448286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116466662-T-C

76448306-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116466682-T-A

76448861-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116467370-G-C

76448958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116467483-G-A

76449123-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116467825-A-T

76450142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116469321-A-G

76450142-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116469321-A-T

76450368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116469504-A-G

76450399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116469531-C-T

76450442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116469578-T-C

76450929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116469747-G-A

76450929-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116469747-G-T

76451391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116470149-C-T

76451669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116470953-C-T

76451758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116471017-A-G

http://identifiers.org/hco/17/GRCh38#76452078-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116471307-C-A

76452198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116471427-G-A

76452373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116471600-A-G

http://identifiers.org/hco/17/GRCh38#76452712-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116471825-C-A

76452712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116471825-C-T

http://identifiers.org/hco/17/GRCh38#76452974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116472087-C-A

76452974-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116472087-C-G

76452974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29554
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116472087-C-T