http://identifiers.org/hco/12/GRCh38#82223733-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105830357-C-A

82225169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105829713-A-G

82225473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105829539-T-C

82225473-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105829539-T-G

82225540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105829485-T-C

82225572-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105829455-G-C

82225940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105828622-G-A

82226091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105828489-G-A

82226224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105828354-G-A

82226372-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105828209-G-C

82226714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105818033-A-G

82227828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105815872-G-A

82227875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105815824-G-A

82227968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105815734-G-A

82228694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105815177-G-A

82228939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105815121-G-A

82228939-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105815121-G-T

82228956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105815104-G-A

82228977-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105815082-A-T

http://identifiers.org/hco/12/GRCh38#82229001-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105815062-C-A

82229001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105815062-C-T

82229297-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105814769-C-G

82229758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105814102-C-T

82238563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105798376-T-C

82238565-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105798374-A-T

http://identifiers.org/hco/12/GRCh38#82238966-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105797997-C-A

82239144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105797838-T-C

82239183-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105797780-C-G

http://identifiers.org/hco/12/GRCh38#82240537-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105797432-C-A

82240676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105797314-A-G

82240730-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105797260-A-T

http://identifiers.org/hco/12/GRCh38#82240793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105797197-C-A

82240836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105797134-G-A

http://identifiers.org/hco/12/GRCh38#82240839-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105797131-A-C

82240839-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105797131-A-T

82240883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105797087-C-T

82240992-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105796996-T-G

82241194-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105796798-G-T

82241223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105796767-T-C

82241224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105796766-A-G

82241269-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105796722-A-T

82241553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105796250-T-C

82241648-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105796161-T-A

82241730-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105796076-G-T

82241950-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105795715-T-G

82249072-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105791781-A-T

http://identifiers.org/hco/12/GRCh38#82249116-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105791740-C-A

82249116-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105791740-C-G

82249213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105791661-T-C

82249221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105791653-G-A

82249221-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105791653-G-T

82249246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105791630-A-G

82249385-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105791515-T-A

82249385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105791515-T-C

82249424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105791499-C-T

82249435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105791488-G-T

82249457-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105791468-G-T

82249557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105791401-G-A

82250074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105790911-C-T

82250076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105790909-G-A

82250076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105790909-G-T

82250190-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105790799-C-G

82250190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105790799-C-T

82250313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105790681-C-T

82250336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105790658-A-G

82259903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105778092-G-A

82259907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105778088-T-C

82259985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105778012-T-C

82260621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105777372-G-A

82260664-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105777320-T-A

82261216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105776639-T-C

82261710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105776157-T-C

82261922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105775955-G-A

82261979-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105775871-T-G

82262003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105775848-A-G

http://identifiers.org/hco/12/GRCh38#82262333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105775421-C-A

82262480-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105775165-T-G

http://identifiers.org/hco/12/GRCh38#82262508-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105775137-A-C

82262581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105775065-G-A

82262581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105775065-G-T

82263907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105774258-T-C

82264005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105773997-T-C

82264603-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105773462-G-C

82264771-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105773274-A-T

82264803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105773252-G-A

82264948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105773109-G-A

82264948-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105773109-G-T

82264989-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105773067-T-G

82265051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105773031-T-C

82265232-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105772874-T-A

http://identifiers.org/hco/12/GRCh38#82265263-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105772843-A-C

82265304-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105772805-T-A

82265304-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105772805-T-G

82265360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105772752-T-C

82265474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105772644-G-A

82265474-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105772644-G-C

82265596-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105772533-T-A

82265632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105772497-T-C

82266942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105770897-C-T

82267141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105770703-C-T

82267225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105770621-G-A

82267305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105770527-C-T

82269047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105770221-T-C

http://identifiers.org/hco/12/GRCh38#82269050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105770218-C-A

82269369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105769987-A-G

82269585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105769576-G-A

82269643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105769510-T-C

82269763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105769399-A-G

82269763-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105769399-A-T

82269782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105769377-A-G

http://identifiers.org/hco/12/GRCh38#82269979-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105769179-A-C

82269997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105769161-G-A

82270429-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105768742-T-G

http://identifiers.org/hco/12/GRCh38#82270575-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105768589-A-C

82270769-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105768411-T-G

82270943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105768238-G-A

82270943-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105768238-G-C

82270973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105768206-A-G

82270978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105768201-T-C

82271007-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105768166-G-T

82275876-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105764855-A-T

82276061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105764681-T-C

82276161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105764427-G-T

82276187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105764384-A-G

82276400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105764202-C-T

82276449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105764153-G-A

82276624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105763990-T-C

82277018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105763641-G-A

82277077-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105763584-T-A

82277077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105763584-T-C

http://identifiers.org/hco/12/GRCh38#82277111-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105763550-A-C

82277117-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105763544-A-T

82277166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105763501-A-G

82277273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105763361-C-T

82277607-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105763052-T-G

82277678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105762987-A-G

http://identifiers.org/hco/12/GRCh38#82278042-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105762625-A-C

82279389-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105752956-T-G

82279987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105752378-G-A

http://identifiers.org/hco/12/GRCh38#82286989-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105751809-C-A

http://identifiers.org/hco/12/GRCh38#82286991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105751807-C-A

82287180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105751627-G-A

82287380-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105751456-C-G

82287380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105751456-C-T

82287531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105751311-A-G

82287631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105751219-A-G

82287931-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105750911-A-T

http://identifiers.org/hco/12/GRCh38#82288037-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105750818-C-A

82288316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105750561-C-T

82288377-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105750457-G-T

82288514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105749984-T-C

82288673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105749822-A-G

82291779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105740442-C-T

82291960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105740258-T-C

http://identifiers.org/hco/12/GRCh38#82292258-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105739886-A-C

82298323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105736771-G-A

82298371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105736722-A-G

82298395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105736698-T-C

82298549-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105736562-A-T

82298558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105736553-T-C

82298764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105736391-A-G

http://identifiers.org/hco/12/GRCh38#82298811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105736360-C-A

82298811-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105736360-C-G

82298811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105736360-C-T

82298812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105736359-G-A

82299955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105735607-G-A

82300025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105735471-A-G

82315571-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105728378-T-G

82315572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105728377-A-G

82315697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105728246-G-A

82315697-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105728246-G-C

82315947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105728025-T-C

http://identifiers.org/hco/12/GRCh38#82316452-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105727563-A-C

82316572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105727463-T-C

82316574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105727461-C-T

82317614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105715721-T-C

82317623-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105715712-G-T

82317915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105715459-G-A

82318185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105715189-T-C

82318185-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105715189-T-G

82318264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105715098-A-G

82318295-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105715069-A-T

82318511-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105714435-T-G

82318650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105714308-G-A

82318655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105714303-G-A

82318725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105714237-A-G

82318747-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105714215-G-C

82318788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105714000-A-G

82319112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105713660-T-C

82319357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105713467-A-G

82319394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105713428-A-G

82319737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105713090-T-C

http://identifiers.org/hco/12/GRCh38#82319896-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105712938-A-C

82320006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105712839-T-C

82320049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105712798-A-G

82320058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105712789-G-A

82320158-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105712687-A-T

82320208-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105712637-G-C

82320208-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105712637-G-T

82320887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105709596-A-G

82321204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105709258-A-G

82321205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105709257-G-A

http://identifiers.org/hco/12/GRCh38#82321353-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105709117-C-A

82321502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105708991-A-G

82321546-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105708953-A-T

82321643-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105708895-G-C

82321756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105708782-T-C

82322088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105708414-C-T

82324993-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105705971-T-G

82325033-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105705930-T-G

82325148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105705819-T-C

82325158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105705809-T-C

82325419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105704565-T-C

82326568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105703945-C-T

82326636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105703872-A-G

82326651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105703857-T-C

http://identifiers.org/hco/12/GRCh38#82326900-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105703608-A-C

82327095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105703406-G-A

82327198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105703297-T-C

http://identifiers.org/hco/12/GRCh38#82327272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105703219-C-A

http://identifiers.org/hco/12/GRCh38#82327339-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105703166-A-C

http://identifiers.org/hco/12/GRCh38#82327342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105703163-C-A

82327487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105703148-A-G

82327493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105703142-A-G

http://identifiers.org/hco/12/GRCh38#82327498-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105703137-A-C

82327503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105703132-A-G

82327503-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105703132-A-T

82327637-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105703060-T-G

82327948-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105702766-C-G

http://identifiers.org/hco/12/GRCh38#82328220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105702242-C-A

82328263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105702200-G-A

82328264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105702199-G-A

82328512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105701963-A-G

82329387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105701055-G-A

82329387-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105701055-G-T

82329405-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105701053-A-T

82329431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105701027-A-G

82329441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105701017-G-A

82334974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105697523-A-G

82334985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105697509-G-A

82335003-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105697491-T-G

82335093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105697409-G-A

82335258-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105697241-T-A

82335311-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105697190-G-T

82339826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105695587-G-A

82340163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105695248-A-G

82340417-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105695061-G-T

82340799-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105694826-T-A

82341093-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105694545-T-A

82341561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105694134-A-G

82341562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105694133-T-C

82341715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105693987-A-G

82341728-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105693974-T-A

82342382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105692921-G-A

82345520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105691084-T-C

82345595-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105691005-T-G

82345873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105690599-T-C

82345873-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105690599-T-G

82346082-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105690427-T-G

82346109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105690400-A-G

82346159-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105690362-T-G

82346206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105690297-C-T

82346345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105690178-A-G

82346753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105689815-T-C

82347487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105688909-C-T

82347713-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105688701-T-G

82348134-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105688332-A-T

82348886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105687732-T-C

82348945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105687644-A-G

82349019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105687571-G-A

82349032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105687561-C-T

82349245-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105687414-T-G

82349425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105687224-C-T

82349714-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105686947-G-C

82349818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105686875-G-A

82349835-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105686858-A-T

82349885-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105686799-T-A

82349891-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105686793-A-T

82349908-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105686779-A-T

82349910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105686777-A-G

82349919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105686768-A-G

82350292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105686412-A-G

82352038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105684128-G-A

http://identifiers.org/hco/12/GRCh38#82352112-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105684076-C-A

82352133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105684055-T-C

82352155-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105684040-G-C

http://identifiers.org/hco/12/GRCh38#82352207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105683992-C-A

82352259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron variant
orthologous variants: 105683937-G-T

http://identifiers.org/hco/12/GRCh38#82352307-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105683891-C-A

82352341-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 105683865-G-T

82352352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 105683854-T-C

82352531-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 105683725-T-A

82352573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 105683680-A-G

82352600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 105683663-A-G

82352600-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 105683663-A-T

82352623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 105683644-A-G

82352656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 105683622-G-A

82352974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 105683203-A-G

http://identifiers.org/hco/12/GRCh38#82352977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105683200-C-A

82353080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 105683117-A-G

82353112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 105683080-A-G

82353314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 105682874-T-C

82353315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 105682873-A-G

http://identifiers.org/hco/12/GRCh38#82353349-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105682839-A-C

82353349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105682839-A-G

http://identifiers.org/hco/12/GRCh38#82354380-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105681410-A-C

http://identifiers.org/hco/12/GRCh38#82354469-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105681334-C-A

82354469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105681334-C-T

82354618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105681187-C-T

82356293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105679443-T-C

82356293-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105679443-T-G

82356299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105679437-C-T

82356564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105679206-A-G

82356685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105678970-A-G

http://identifiers.org/hco/12/GRCh38#82356706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105678952-C-A

82356706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105678952-C-T

http://identifiers.org/hco/12/GRCh38#82356710-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105678948-A-C

http://identifiers.org/hco/12/GRCh38#82356720-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105678938-A-C

http://identifiers.org/hco/12/GRCh38#82356785-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105678873-C-A

82356785-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105678873-C-G

http://identifiers.org/hco/12/GRCh38#82356791-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105678867-C-A

http://identifiers.org/hco/12/GRCh38#82356832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105678830-C-A

http://identifiers.org/hco/12/GRCh38#82356833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105678829-C-A

82356833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105678829-C-T

82356888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105678783-T-C

82356890-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105678781-T-A

82356890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105678781-T-C

82356896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105678775-A-G

82356896-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105678775-A-T

82356913-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105678765-A-T

82356934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105678733-G-A

82356934-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105678733-G-T

http://identifiers.org/hco/12/GRCh38#82356949-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105678718-A-C

82356949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105678718-A-G

82356990-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 105678683-T-G

82356998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 105678675-G-A

82356998-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 105678675-G-C

http://identifiers.org/hco/12/GRCh38#82357009-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105678664-A-C

82357009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 105678664-A-G

http://identifiers.org/hco/12/GRCh38#82357024-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105678649-A-C

82357060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 105678613-G-A

82357060-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 105678613-G-T

82357209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 105678461-C-T

82357286-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105678383-C-G

82357429-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105678268-T-A

82357430-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105678267-G-C

82357430-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105678267-G-T

82357470-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105678227-G-C

82357576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105678125-T-C

82357852-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105677834-T-G

82357873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105677813-G-A

82357875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105677811-G-A

82357877-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105677809-A-T

82358072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105677627-A-G

82358098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105677601-A-G

http://identifiers.org/hco/12/GRCh38#82358106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#105677593-C-A

82358106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105677593-C-T

82358224-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 105677513-C-G

82358224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant, undefined
orthologous variants: 105677513-C-T

82358234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105677503-C-T

82358310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 105677427-A-G

82358322-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 105677415-C-G

http://identifiers.org/hco/12/GRCh38#82358328-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#105677409-C-A

82358328-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 105677409-C-G

82358328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 105677409-C-T

http://identifiers.org/hco/12/GRCh38#82358349-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#105677388-A-C

82358351-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 105677386-T-G

82358356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 105677381-G-A

82358356-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 105677381-G-C

82358356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 105677381-G-T

http://identifiers.org/hco/12/GRCh38#82358358-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#105677379-A-C

82358358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 105677379-A-G

82358378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 105677359-G-T

http://identifiers.org/hco/12/GRCh38#82358379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#105677358-C-A

82358387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 105677350-T-C

82358387-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 105677350-T-G

82358438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105677301-G-T

http://identifiers.org/hco/12/GRCh38#82358486-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#105677253-A-C

82358486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105677253-A-G

82358594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 105677141-C-T

82358683-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 105677052-G-C

82358768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 105676973-A-G

82358768-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 105676973-A-T

82358776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 105676965-G-A

82358792-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 105676958-C-G

82358792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25005
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 105676958-C-T