http://identifiers.org/hco/4/GRCh38#76709122-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93066103-C-A

76709122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93066103-C-T

76709198-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93066176-C-G

76709208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93066186-G-A

76709641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93066917-G-T

76709795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93067082-G-A

76709795-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93067082-G-C

76709795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93067082-G-T

http://identifiers.org/hco/4/GRCh38#76709957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93067344-C-A

76709957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93067344-C-T

76709969-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93067350-T-G

76710042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93067396-T-C

76710096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93067442-T-C

76710100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93067446-T-C

76710119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93067466-C-T

76710120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93067467-A-G

76710423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93067740-A-G

76711600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93068230-G-A

76711684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93068336-A-G

76714218-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93070875-C-G

76714254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93070913-C-T

76714488-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93071633-G-C

76714869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93072013-A-G

76714875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93072019-G-A

76714875-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93072019-G-C

76714900-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93072044-A-T

http://identifiers.org/hco/4/GRCh38#76714983-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93072111-A-C

76715186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93072282-T-C

76715389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93072510-G-A

76715480-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93072615-C-G

76715737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93072823-A-G

http://identifiers.org/hco/4/GRCh38#76716213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#93073155-C-A

76716250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93073197-G-A

76716320-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93073258-A-T

76716322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93073260-C-T

76716348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93073286-G-A

76716348-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93073286-G-C

76716348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93073286-G-T

76716374-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93073306-G-C

76716465-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93073383-C-G

76716465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93073383-C-T

76716590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93073703-T-C

76716722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93073839-A-G

76716736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93073853-C-T

76717263-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93075210-G-T

76717324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93075267-T-C

http://identifiers.org/hco/4/GRCh38#76718201-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93075995-A-C

76718292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93076074-A-G

76718432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93076222-T-C

http://identifiers.org/hco/4/GRCh38#76718790-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93076537-A-C

76718831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93076569-T-C

76718859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93076597-C-T

http://identifiers.org/hco/4/GRCh38#76718879-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93076620-A-C

76720051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93077152-G-A

76720051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93077152-G-T

76720059-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93077162-C-G

76720059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93077162-C-T

76722962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93077933-G-A

http://identifiers.org/hco/4/GRCh38#76723133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93078601-C-A

76723169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93078642-T-C

76728771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93080317-C-T

76730058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93080976-C-T

76730203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93081090-G-A

76730268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93081156-C-T

76730432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93081335-T-C

76730765-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93081573-T-G

76730813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93081622-G-A

76730972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93081781-T-C

http://identifiers.org/hco/4/GRCh38#76731226-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93081975-A-C

76731247-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93081996-T-G

76731292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93082039-G-A

76732114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93082595-A-G

76732317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93082780-C-T

76732412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93082856-C-T

76732498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93082923-T-C

76732522-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93082948-T-A

76732601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93083023-G-A

76732601-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93083023-G-C

76732603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93083025-G-A

76732693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93083092-A-G

76732741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93083115-G-A

76732743-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93083117-C-G

76732743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93083117-C-T

76732783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93083157-C-T

http://identifiers.org/hco/4/GRCh38#76732860-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93083230-A-C

76733021-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93083353-T-G

76733033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93083365-G-A

76733156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93083489-A-G

76733410-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93083711-G-C

76733474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93083772-T-C

76733474-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93083772-T-G

76733735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93084002-C-T

76733746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93084014-C-T

76733784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93084048-G-A

76733796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93084060-G-A

76734298-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93084518-T-A

76734341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93084546-T-C

76734456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93084658-T-C

76734516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93084732-T-C

76734602-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93084827-C-G

76734826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93085100-G-A

76734906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93085172-T-C

76734974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93085244-C-T

76735000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93085269-A-G

76735014-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93085279-C-G

76735098-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93085362-T-A

76735301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93085535-A-G

76735344-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93085579-C-G

76735504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93085734-T-C

76736443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93086230-C-T

http://identifiers.org/hco/4/GRCh38#76736589-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93086366-A-C

76736589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93086366-A-G

76738184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93087253-C-T

76738284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93087352-G-A

76738305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93087373-C-T

http://identifiers.org/hco/4/GRCh38#76738306-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#93087374-A-C

76738306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93087374-A-G

http://identifiers.org/hco/4/GRCh38#76738369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93087446-C-A

76738369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93087446-C-T

http://identifiers.org/hco/4/GRCh38#76738591-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93087681-A-C

http://identifiers.org/hco/4/GRCh38#76738709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93087783-C-A

http://identifiers.org/hco/4/GRCh38#76738791-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#93087866-C-A

76738863-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93087938-G-C

76739160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93088238-G-A

76739331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93088409-A-G

76739365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93088443-C-T

http://identifiers.org/hco/4/GRCh38#76739541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#93088619-C-A

76739541-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93088619-C-G

76739655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93088733-A-G

76739748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93088826-G-A

76739748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93088826-G-T

76739787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93088865-G-A

http://identifiers.org/hco/4/GRCh38#76739898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#93088970-C-A

76739898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93088970-C-T

76739946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93089018-C-T

76739950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93089022-A-G

76739962-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93089037-T-A

76739979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93089054-C-T

http://identifiers.org/hco/4/GRCh38#76740008-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#93089083-A-C

76740048-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93089123-C-G

76740048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93089123-C-T

76740126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93089201-G-A

http://identifiers.org/hco/4/GRCh38#76740238-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#93089310-C-A

76740238-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93089310-C-G

76740368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93089425-C-T

http://identifiers.org/hco/4/GRCh38#76740415-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#93089472-C-A

76740415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93089472-C-T

76740426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93089483-G-A

76740426-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93089483-G-C

76740426-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93089483-G-T

76740435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93089492-C-T

76740451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93089508-G-A

76740474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93089531-G-A

76740474-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93089531-G-C

76740474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93089531-G-T

76740495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93089543-C-T

76740584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93089635-G-A

76740585-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93089636-T-A

http://identifiers.org/hco/4/GRCh38#76740609-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#93089660-C-A

76740609-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93089660-C-G

76740609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93089660-C-T

http://identifiers.org/hco/4/GRCh38#76740618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#93089669-C-A

76740618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93089669-C-T

76740622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93089673-A-G

76740677-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93089731-C-G

76740677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93089731-C-T

76740746-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93089800-C-G

76740752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93089814-G-A

76740771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93089838-G-A

76740778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93089850-G-A

76740789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93089861-G-A

76740789-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93089861-G-T

http://identifiers.org/hco/4/GRCh38#76740798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#93089870-C-A

76740798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93089870-C-T

http://identifiers.org/hco/4/GRCh38#76740900-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#93089975-C-A

76740930-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93090005-C-G

76740930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93090005-C-T

76740948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93090023-G-A

76740948-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93090023-G-T

76740966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93090041-A-G

76740966-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93090041-A-T

76741017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93090092-G-A

76741017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93090092-G-T

http://identifiers.org/hco/4/GRCh38#76741100-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#93090178-C-A

76741100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93090178-C-T

76741143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93090221-T-C

76741245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93090302-G-A

76741285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93090342-G-A

76741285-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93090342-G-C

76741299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93090356-G-A

76741299-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93090356-G-T

76741313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93090373-T-C

http://identifiers.org/hco/4/GRCh38#76741389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#93090449-C-A

76741389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93090449-C-T

http://identifiers.org/hco/4/GRCh38#76741401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#93090461-C-A

76741401-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93090461-C-G

76741401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93090461-C-T

76741413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93090473-G-A

76741413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93090473-G-T

http://identifiers.org/hco/4/GRCh38#76741427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#93090487-C-A

76741427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93090487-C-T

http://identifiers.org/hco/4/GRCh38#76741455-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#93090515-C-A

76741455-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93090515-C-G

76741455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93090515-C-T

76741468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93090528-A-G

http://identifiers.org/hco/4/GRCh38#76741491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#93090545-C-A

76741491-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93090545-C-G

76741491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93090545-C-T

76741518-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93090569-C-G

76741518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93090569-C-T

76741519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93090570-G-A

76741519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93090570-G-T

http://identifiers.org/hco/4/GRCh38#76741536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#93090587-C-A

76741543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93090594-G-A

76741543-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93090594-G-C

76741543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93090594-G-T

76741551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93090602-G-A

76741551-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93090602-G-C

76741551-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93090602-G-T

http://identifiers.org/hco/4/GRCh38#76741566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#93090617-C-A

76741566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93090617-C-T

76741578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93090629-G-A

76741578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93090629-G-T

76741584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93090635-C-T

76741613-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93090664-T-A

76741613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93090664-T-C

76741614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93090665-G-A

76741614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93090665-G-T

76741633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93090684-A-G

76741653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93090698-T-C

76741677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93090722-A-G

76741757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93090820-G-A

76741757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93090820-G-T

http://identifiers.org/hco/4/GRCh38#76741791-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#93090854-C-A

76741815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93090884-C-T

http://identifiers.org/hco/4/GRCh38#76741839-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#93090911-C-A

76741839-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93090911-C-G

76741839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93090911-C-T

76741860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93090932-G-A

76741860-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93090932-G-C

76741860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93090932-G-T

76741885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93090957-G-A

76741885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93090957-G-T

76741967-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93091040-C-G

76741985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93091059-T-C

76742079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93091145-T-C

http://identifiers.org/hco/4/GRCh38#76742083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93091149-C-A

76742089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93091155-T-C

76742106-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93091180-T-A

76742106-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93091180-T-G

76742107-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93091181-T-A

76742107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93091181-T-C

76744317-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93092347-T-A

76744693-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93092749-T-A

76744892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93092871-C-T

76744940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93092907-G-A

76744940-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93092907-G-C

http://identifiers.org/hco/4/GRCh38#76745323-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93093293-A-C

76745449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93093356-G-A

76745486-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93093384-C-G

76745572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93093456-A-G

76745655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93093543-G-A

76747392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93094673-T-C

76747631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93094985-G-A

76747982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93095317-A-G

http://identifiers.org/hco/4/GRCh38#76747993-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93095333-C-A

76748118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93095438-G-A

76748205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93095875-G-A

76749041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93096287-G-A

76749042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93096288-G-T

76753246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93097390-A-G

http://identifiers.org/hco/4/GRCh38#76753566-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93097689-A-C

76754037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93098183-G-T

76754047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93098193-C-T

76754151-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93098271-T-G

76754270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93098302-T-C

http://identifiers.org/hco/4/GRCh38#76754359-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#93098391-C-A

76754359-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93098391-C-G

76754360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93098392-C-T

76754434-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93098466-T-G

76754435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93098467-G-A

76754463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93098492-G-A

76754470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93098499-A-G

76754618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93098647-C-T

76754675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93098677-C-T

76754721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93098723-A-G

76754789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93098791-G-A

76754800-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93098802-G-C

http://identifiers.org/hco/4/GRCh38#76754839-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#93098841-A-C

76754871-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93098873-T-A

http://identifiers.org/hco/4/GRCh38#76755073-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#93099054-A-C

76755073-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93099054-A-T

http://identifiers.org/hco/4/GRCh38#76755127-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#93099111-A-C

76755159-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93099146-T-A

76755159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93099146-T-C

76755185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93099172-C-T

http://identifiers.org/hco/4/GRCh38#76755243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93099234-C-A

76755258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93099242-G-A

http://identifiers.org/hco/4/GRCh38#76755264-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93099248-C-A

76755264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93099248-C-T

http://identifiers.org/hco/4/GRCh38#76755271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93099255-C-A

76755271-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93099255-C-G

76755271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93099255-C-T

http://identifiers.org/hco/4/GRCh38#76755283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93099267-C-A

76755283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93099267-C-T

76755326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93099308-T-C

76755380-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93099352-T-G

76755647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93099629-G-A

http://identifiers.org/hco/4/GRCh38#76755688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93099670-C-A

76755688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93099670-C-T

76755691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93099673-C-T

76755730-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93099702-G-T

76755731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93099703-G-A

http://identifiers.org/hco/4/GRCh38#76756300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93100279-C-A

76756300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93100279-C-T

76756301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93100280-A-G

76756328-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93100303-A-T

http://identifiers.org/hco/4/GRCh38#76756333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93100308-C-A

http://identifiers.org/hco/4/GRCh38#76756334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93100309-C-A

http://identifiers.org/hco/4/GRCh38#76756354-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93100322-C-A

76756354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93100322-C-T

76756358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93100326-G-A

76756551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93100503-T-C

76756552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93100504-A-G

76756562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93100514-C-T

76756570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93100522-G-A

76756597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93100549-G-A

76756597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93100549-G-T

76756652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93100604-A-G

76756701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93100653-A-G

76756711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93100663-G-A

76756711-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93100663-G-C

76756809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93100761-C-T

76756812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93100764-G-A

76756845-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93100797-G-C

76756954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93100906-G-A

76756990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93100938-G-A

76756990-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93100938-G-C

76757041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93100979-G-A

76757041-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93100979-G-C

76757098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93101020-A-G

http://identifiers.org/hco/4/GRCh38#76757157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93101073-C-A

76757157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93101073-C-T

76757408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93101265-C-T

76757470-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93101325-C-G

76757470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93101325-C-T

76757598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93101445-C-T

76757884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93101776-G-A

76757941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93101833-G-A

76758088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93101975-G-A

76758165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93102048-T-C

76758227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93102107-C-T

76758241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 93102121-G-A

http://identifiers.org/hco/4/GRCh38#76758309-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93102226-C-A

76758790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93102632-A-G

76759341-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93102984-G-T

76759509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93103106-T-C

76759512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93103109-G-A

76759680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93103255-T-C

76759764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93103326-G-A

76759764-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93103326-G-C

76759764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93103326-G-T

76759793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93103359-G-A

76760181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93103608-C-T

76760229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93103656-G-A

76760504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93103888-T-C

76760569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93103946-G-A

76766375-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93107675-T-A

76766378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93107678-T-C

76766578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93107866-G-A

76768875-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93109223-G-C

76770490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93109821-G-A

76770490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93109821-G-T

http://identifiers.org/hco/4/GRCh38#76770499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93109831-C-A

76770499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93109831-C-T

76770519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93109848-T-C

76770537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93109866-A-G

http://identifiers.org/hco/4/GRCh38#76770576-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93109902-C-A

76770880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93110204-T-C

76770886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93110210-T-C

76774926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93111244-T-C

76777886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93111461-C-T

76778707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93112133-G-A

76778707-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93112133-G-C

76778767-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93112174-C-G

76778850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93112256-T-C

http://identifiers.org/hco/4/GRCh38#76778859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#93112265-C-A

76778880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93112286-G-A

76778931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93112337-G-A

76779096-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93112502-C-G

76779096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93112502-C-T

76779126-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93112532-T-G

76779129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93112535-G-A

76779141-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93112547-C-G

76779141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93112547-C-T

76779146-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93112552-G-C

76779146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93112552-G-T

http://identifiers.org/hco/4/GRCh38#76779178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#93112584-C-A

http://identifiers.org/hco/4/GRCh38#76779198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#93112604-C-A

76779198-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93112604-C-G

http://identifiers.org/hco/4/GRCh38#76779257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#93112659-C-A

76779257-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93112659-C-G

76779258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93112660-T-C

76779259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93112661-G-A

76779259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93112661-G-T

76779278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93112678-T-C

76779295-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93112693-T-A

76779349-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93112735-G-T

76779373-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93112759-G-T

76779415-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93112767-A-T

76779449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93112799-G-A

76779449-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93112799-G-T

76779452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93112802-G-A

76779452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93112802-G-T

76779483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93112830-C-T

76780029-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93113537-G-T

76780084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93113579-A-G

http://identifiers.org/hco/4/GRCh38#76780094-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#93113589-C-A

76780094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93113589-C-T

76780250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93113703-G-T

76780324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93113774-G-T

76780325-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93113775-G-T

76780333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93113787-G-A

76780333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93113787-G-T

76780392-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93113844-G-T

76780469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93113877-T-C

76780713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93113912-A-G

76780736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93113929-T-C

76780745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93113938-G-T

76780751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93113944-A-G

76780811-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93113992-A-T

76780832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93114016-G-T

http://identifiers.org/hco/4/GRCh38#76780853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#93114030-C-A

76780873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93114051-G-A

76780873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93114051-G-T

76780907-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93114068-T-A

76780907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93114068-T-C

http://identifiers.org/hco/4/GRCh38#76780950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#93114097-C-A

76780950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93114097-C-T

http://identifiers.org/hco/4/GRCh38#76781427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#93114661-C-A

76781485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93114712-T-C

76781529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93114750-T-C

76781536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93114757-G-A

76781616-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93114839-T-G

76781814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93115030-A-G

76781948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93115138-C-T

76781950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93115140-C-T

76781981-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93115159-G-C

76781981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93115159-G-T

76782031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93115205-G-A

76782031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93115205-G-T

76782093-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93115245-G-T

76782180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93115325-G-A

http://identifiers.org/hco/4/GRCh38#76782252-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#93115366-C-A

76782270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93115397-G-T

http://identifiers.org/hco/4/GRCh38#76782284-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#93115411-C-A

76782284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93115411-C-T

http://identifiers.org/hco/4/GRCh38#76782396-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#93115466-A-C

76782682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93116048-C-T

76782709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93116075-A-G

76782770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93116135-G-A

76782796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93116149-A-G

76782961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93116879-G-A

76782961-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93116879-G-C

76782968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93116886-A-G

76782986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93116904-G-A

76782988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93116906-T-C

http://identifiers.org/hco/4/GRCh38#76782992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#93116910-C-A

76782992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93116910-C-T

76783004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93116923-T-C

http://identifiers.org/hco/4/GRCh38#76783069-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#93117054-C-A

76783094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93117182-A-G

76783118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93117206-C-T

76783445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93117415-C-T

76783568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93117506-T-C

76783596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93117518-T-C

http://identifiers.org/hco/4/GRCh38#76783718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#93117635-C-A

76783726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93117643-T-C

76783729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93117646-A-G

76784033-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93117921-G-C

76784352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93118148-G-A

76784416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93118214-C-T

76784442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93118585-G-A

76784571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93118673-C-T

76784653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93118741-A-G

76784714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93118855-G-A

76784820-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41265
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93118954-T-A