141657087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: 3 prime UTR variant
orthologous variants: 40378660-A-G

141657207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: 3 prime UTR variant
orthologous variants: 40378784-C-T

141657271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: 3 prime UTR variant
orthologous variants: 40378845-T-C

http://identifiers.org/hco/7/GRCh38#141657298-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40378874-C-A

141657528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: 3 prime UTR variant
orthologous variants: 40379077-G-A

141657839-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: 3 prime UTR variant
orthologous variants: 40379353-T-G

http://identifiers.org/hco/7/GRCh38#141657893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40379407-C-A

141657893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: 3 prime UTR variant
orthologous variants: 40379407-C-T

141658062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: 3 prime UTR variant
orthologous variants: 40379574-A-G

141658062-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: 3 prime UTR variant
orthologous variants: 40379574-A-T

141658097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: 3 prime UTR variant
orthologous variants: 40379612-A-G

141658221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: 3 prime UTR variant
orthologous variants: 40379732-T-C

141658313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: 3 prime UTR variant
orthologous variants: 40379821-G-T

141658314-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: 3 prime UTR variant
orthologous variants: 40379822-T-A

http://identifiers.org/hco/7/GRCh38#141658428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40379933-C-A

141658644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: 3 prime UTR variant
orthologous variants: 40380101-A-G

141658644-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: 3 prime UTR variant
orthologous variants: 40380101-A-T

141658669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: 3 prime UTR variant
orthologous variants: 40380131-T-C

141658721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: 3 prime UTR variant
orthologous variants: 40380182-T-C

http://identifiers.org/hco/7/GRCh38#141658846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40380294-C-A

141659009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: 3 prime UTR variant
orthologous variants: 40380454-T-C

141659020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: 3 prime UTR variant
orthologous variants: 40380462-A-G

141659026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: 3 prime UTR variant
orthologous variants: 40380468-G-A

141659222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: 3 prime UTR variant
orthologous variants: 40380622-A-G

http://identifiers.org/hco/7/GRCh38#141659364-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40380762-C-A

141659364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: 3 prime UTR variant
orthologous variants: 40380762-C-T

141659422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: 3 prime UTR variant
orthologous variants: 40380823-T-C

141659509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: 3 prime UTR variant
orthologous variants: 40380890-C-T

http://identifiers.org/hco/7/GRCh38#141659547-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40380942-C-A

141659552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: 3 prime UTR variant
orthologous variants: 40380947-G-A

http://identifiers.org/hco/7/GRCh38#141659571-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40380982-C-A

141659571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: 3 prime UTR variant
orthologous variants: 40380982-C-T

141659617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: 3 prime UTR variant
orthologous variants: 40381019-A-G

141659626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: 3 prime UTR variant
orthologous variants: 40381028-A-G

http://identifiers.org/hco/7/GRCh38#141659655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40381057-C-A

141659655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: 3 prime UTR variant
orthologous variants: 40381057-C-T

141659688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: 3 prime UTR variant
orthologous variants: 40381090-G-T

http://identifiers.org/hco/7/GRCh38#141659715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40381111-C-A

141659715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: 3 prime UTR variant
orthologous variants: 40381111-C-T

141659846-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: 3 prime UTR variant
orthologous variants: 40381231-G-C

141659928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: 3 prime UTR variant
orthologous variants: 40381311-A-G

http://identifiers.org/hco/7/GRCh38#141660180-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40381558-C-A

141660180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: 3 prime UTR variant
orthologous variants: 40381558-C-T

http://identifiers.org/hco/7/GRCh38#141660205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40381581-C-A

141660221-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: 3 prime UTR variant
orthologous variants: 40381597-G-T

141660235-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: 3 prime UTR variant
orthologous variants: 40381611-G-T

http://identifiers.org/hco/7/GRCh38#141660260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40381628-C-A

141660724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: 3 prime UTR variant
orthologous variants: 40382102-G-A

141660724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: 3 prime UTR variant
orthologous variants: 40382102-G-T

141660730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: 3 prime UTR variant
orthologous variants: 40382107-A-G

http://identifiers.org/hco/7/GRCh38#141660829-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40382208-C-A

141660936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: 3 prime UTR variant
orthologous variants: 40382310-A-G

141661058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: 3 prime UTR variant
orthologous variants: 40382430-C-T

http://identifiers.org/hco/7/GRCh38#141661355-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40382605-C-A

141661355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: 3 prime UTR variant
orthologous variants: 40382605-C-T

141661368-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: 3 prime UTR variant
orthologous variants: 40382625-G-T

http://identifiers.org/hco/7/GRCh38#141661422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40382678-C-A

141661422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: 3 prime UTR variant
orthologous variants: 40382678-C-T

141661452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: 3 prime UTR variant
orthologous variants: 40382701-G-A

141661452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: 3 prime UTR variant
orthologous variants: 40382701-G-T

141661469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: 3 prime UTR variant
orthologous variants: 40382718-C-T

141661496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: 3 prime UTR variant
orthologous variants: 40382746-A-G

141661553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: 3 prime UTR variant
orthologous variants: 40382793-T-C

http://identifiers.org/hco/7/GRCh38#141661645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40382879-C-A

141661645-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: 3 prime UTR variant
orthologous variants: 40382879-C-G

141661697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: 3 prime UTR variant
orthologous variants: 40382936-C-T

http://identifiers.org/hco/7/GRCh38#141661830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40383009-C-A

141661830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: 3 prime UTR variant
orthologous variants: 40383009-C-T

141661847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: 3 prime UTR variant
orthologous variants: 40383025-C-T

141662243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: 3 prime UTR variant
orthologous variants: 40383268-G-T

141662329-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: 3 prime UTR variant
orthologous variants: 40383357-C-G

141662402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: 3 prime UTR variant
orthologous variants: 40383417-C-T

141662423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: 3 prime UTR variant
orthologous variants: 40383435-A-G

141662488-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: 3 prime UTR variant
orthologous variants: 40383493-T-A

141662488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: 3 prime UTR variant
orthologous variants: 40383493-T-C

141662534-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: 3 prime UTR variant
orthologous variants: 40383551-G-C

http://identifiers.org/hco/7/GRCh38#141662621-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40383634-C-A

141662621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: 3 prime UTR variant
orthologous variants: 40383634-C-T

http://identifiers.org/hco/7/GRCh38#141662622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40383635-C-A

141662622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: 3 prime UTR variant
orthologous variants: 40383635-C-T

http://identifiers.org/hco/7/GRCh38#141662930-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#40383933-C-A

141662930-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron_variant, undefined
orthologous variants: 40383933-C-G

http://identifiers.org/hco/7/GRCh38#141662939-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#40383942-A-C

141662939-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron_variant, undefined
orthologous variants: 40383942-A-G

141662956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron_variant, undefined
orthologous variants: 40383955-A-G

http://identifiers.org/hco/7/GRCh38#141663003-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#40384001-A-C

141663003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron_variant, undefined
orthologous variants: 40384001-A-G

http://identifiers.org/hco/7/GRCh38#141663012-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#40384009-A-C

141663012-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron_variant, undefined
orthologous variants: 40384009-A-T

http://identifiers.org/hco/7/GRCh38#141663034-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#40384029-C-A

141663083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron_variant, undefined
orthologous variants: 40384066-G-A

141663083-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron_variant, undefined
orthologous variants: 40384066-G-C

141663083-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron_variant, undefined
orthologous variants: 40384066-G-T

http://identifiers.org/hco/7/GRCh38#141663535-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#40384604-A-C

http://identifiers.org/hco/7/GRCh38#141663542-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#40384611-A-C

http://identifiers.org/hco/7/GRCh38#141663572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#40384646-C-A

http://identifiers.org/hco/7/GRCh38#141663629-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#40384716-C-A

141663629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron_variant, undefined
orthologous variants: 40384716-C-T

http://identifiers.org/hco/7/GRCh38#141663690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#40384753-C-A

141663767-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron_variant, undefined
orthologous variants: 40384817-G-C

141663839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron_variant, undefined
orthologous variants: 40384891-A-G

141663917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40384952-A-G

http://identifiers.org/hco/7/GRCh38#141663946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40384978-C-A

141663946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40384978-C-T

http://identifiers.org/hco/7/GRCh38#141663949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40384981-C-A

http://identifiers.org/hco/7/GRCh38#141664027-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40385054-C-A

141664027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40385054-C-T

141664031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40385058-T-C

141664109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40385132-G-T

141664120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40385152-A-G

141664120-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40385152-A-T

http://identifiers.org/hco/7/GRCh38#141664162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40385191-C-A

141664162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40385191-C-T

141664195-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: synonymous variant
orthologous variants: 40385226-A-T

141664289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40385319-G-A

141664289-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40385319-G-T

141664345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40385372-A-G

http://identifiers.org/hco/7/GRCh38#141664559-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40385653-C-A

141664700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40385773-C-T

http://identifiers.org/hco/7/GRCh38#141664793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40385828-C-A

http://identifiers.org/hco/7/GRCh38#141664819-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40385846-C-A

141664819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40385846-C-T

141664834-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40385864-G-C

141664834-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40385864-G-T

141664876-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40385917-C-G

141664876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40385917-C-T

141665069-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40386158-G-T

141665348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40386434-G-A

141665348-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40386434-G-C

http://identifiers.org/hco/7/GRCh38#141665362-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40386448-C-A

141665362-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40386448-C-G

141665362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40386448-C-T

141666089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40388353-G-A

http://identifiers.org/hco/7/GRCh38#141666240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40388495-C-A

141666260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40388515-G-A

141666369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: synonymous variant
orthologous variants: 40388622-G-A

141666452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40388688-G-A

http://identifiers.org/hco/7/GRCh38#141666755-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40388990-C-A

141667512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40389807-C-T

141667796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40390086-G-A

141667917-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40390216-C-G

141668037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40390333-C-T

141668053-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40390348-A-T

141668093-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40390381-T-A

141671017-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40392108-G-C

141671618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40392461-A-G

141671644-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40392487-A-T

141671709-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40392545-T-G

141671834-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40392639-C-G

141672372-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40393152-T-A

141673135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40394258-C-T

141673392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40394469-C-T

141673506-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40394905-G-C

141673694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40395085-G-A

141673745-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40395133-T-A

http://identifiers.org/hco/7/GRCh38#141674076-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40395435-A-C

141674097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: synonymous variant
orthologous variants: 40395456-G-A

141674097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: synonymous variant
orthologous variants: 40395456-G-T

141674202-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: synonymous variant
orthologous variants: 40395561-T-A

141674259-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40395599-A-T

141674316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40395641-G-A

141674345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40395655-T-C

141674421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40395730-G-A

141674806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40396073-C-T

141674976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40396208-G-A

141675019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40396253-G-A

141675182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40396398-G-A

141675182-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40396398-G-C

141675362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40396550-T-C

141675398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40396575-C-T

141675500-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40396674-C-G

141675714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40396863-C-T

141675737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40396886-C-T

141675749-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40396898-T-G

141675803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40396955-A-G

141675818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40396970-T-C

141675828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40396980-T-C

http://identifiers.org/hco/7/GRCh38#141676013-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40397267-C-A

141676025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40397279-A-G

141676162-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40397381-C-G

141676443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40397489-C-T

http://identifiers.org/hco/7/GRCh38#141676578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40397725-C-A

141676578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40397725-C-T

141676738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40397869-T-C

141684822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40399206-G-A

141685058-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40399251-A-T

141685170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40399354-T-C

141685294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40399466-G-A

141685358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40399530-G-A

141685358-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40399530-G-C

141685358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40399530-G-T

141685576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: synonymous variant
orthologous variants: 40399758-G-A

141685606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: synonymous variant
orthologous variants: 40399788-C-T

http://identifiers.org/hco/7/GRCh38#141685744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40399954-C-A

141685825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40400040-T-C

141685828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40400043-G-A

141685832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40400047-G-A

141686058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40400269-C-T

141686314-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40400469-T-A

http://identifiers.org/hco/7/GRCh38#141686393-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40400517-C-A

141686493-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40400596-A-T

141686497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40400600-T-C

141686497-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40400600-T-G

141686516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40400619-G-A

141686516-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40400619-G-C

141686516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40400619-G-T

http://identifiers.org/hco/7/GRCh38#141686588-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40400687-A-C

141686712-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40400811-G-C

http://identifiers.org/hco/7/GRCh38#141686735-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40400827-C-A

141686738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40400830-G-T

141686754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40400845-G-A

141686754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40400845-G-T

141686759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40400850-C-T

141686773-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40400857-G-C

141686773-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40400857-G-T

141686782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40400873-G-A

http://identifiers.org/hco/7/GRCh38#141686959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40400999-C-A

141686959-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40400999-C-G

141686959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40400999-C-T

141687016-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40401071-T-A

141687175-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40401363-T-A

141687175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40401363-T-C

141687345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40401515-G-A

141687380-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40401541-T-A

141687380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40401541-T-C

141688174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40401706-A-G

141688287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40401813-A-G

141688474-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40402002-T-A

141689703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40402464-T-C

141689751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40402523-C-T

141689960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40402715-T-C

141690195-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40402932-C-G

141690404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40403258-C-T

141690562-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40403391-C-G

141690576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40403403-C-T

141690624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40403438-C-T

141691079-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40404045-G-C

141691357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40404306-T-C

141691477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40404424-C-T

141691603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40404547-C-T

141692054-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40405057-T-A

141694785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40405516-C-T

141694806-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40405530-G-C

141694952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40405657-C-T

141695024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40405721-G-A

141695122-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40405848-T-G

http://identifiers.org/hco/7/GRCh38#141695486-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40406280-C-A

141695525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40406317-T-C

141695847-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron_variant, undefined
orthologous variants: 40406619-C-G

141696117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron_variant, undefined
orthologous variants: 40406874-T-C

141696481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40407320-G-T

141696722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40407733-T-C

141696728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40407739-C-T

141696813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40407832-C-T

141696855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40407860-G-A

141697211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40408162-C-T

141697360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40408311-G-A

141697510-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40408457-A-T

http://identifiers.org/hco/7/GRCh38#141697722-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40408634-A-C

141697722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40408634-A-G

141697876-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40408881-G-C

http://identifiers.org/hco/7/GRCh38#141697929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40408932-C-A

http://identifiers.org/hco/7/GRCh38#141698253-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40409274-C-A

141698494-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40409510-G-C

141698597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40409647-G-A

http://identifiers.org/hco/7/GRCh38#141698741-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40410048-A-C

141698857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40410207-C-T

http://identifiers.org/hco/7/GRCh38#141698906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40410256-C-A

141698907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40410257-A-G

141698925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40410274-C-T

141698926-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40410275-A-T

141698956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40410290-G-A

http://identifiers.org/hco/7/GRCh38#141699396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40410706-C-A

141699417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40410727-T-C

http://identifiers.org/hco/7/GRCh38#141699542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40410844-C-A

141699609-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40410889-C-G

141699681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40410960-T-C

141699835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40411085-T-C

141699837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40411087-T-C

141699919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40411235-C-T

141699944-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40411260-T-A

141700626-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40411680-T-A

141700626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40411680-T-C

141700773-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40411828-C-G

141700950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40412036-C-T

141700953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40412039-G-A

141701011-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40412059-C-G

141701044-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40412084-C-G

141701171-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40412198-G-C

141701485-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron_variant, undefined
orthologous variants: 40412417-T-G

141701513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40412448-T-C

http://identifiers.org/hco/7/GRCh38#141701555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron_variant, splice_donor_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#40412501-C-A

141701555-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron_variant, splice_donor_variant, undefined
orthologous variants: 40412501-C-G

141701555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron_variant, splice_donor_variant, undefined
orthologous variants: 40412501-C-T

http://identifiers.org/hco/7/GRCh38#141701614-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40412557-A-C

141701759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron_variant, undefined
orthologous variants: 40412663-G-A

141701759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron_variant, undefined
orthologous variants: 40412663-G-T

141701773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40412670-G-A

141701773-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40412670-G-T

141701807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40412704-G-A

141701807-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40412704-G-C

141701807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40412704-G-T

http://identifiers.org/hco/7/GRCh38#141701825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40412722-C-A

141701825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40412722-C-T

141701858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40412764-A-G

http://identifiers.org/hco/7/GRCh38#141701876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40412782-C-A

141701876-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40412782-C-G

141701876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: intron variant
orthologous variants: 40412782-C-T

141701890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: synonymous variant
orthologous variants: 40412796-G-A

141701890-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: synonymous variant
orthologous variants: 40412796-G-C

141701890-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: synonymous variant
orthologous variants: 40412796-G-T

141702030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: missense variant
orthologous variants: 40412936-G-A

141702030-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: missense variant
orthologous variants: 40412936-G-T

141702037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: synonymous variant
orthologous variants: 40412943-G-A

141702037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29472
most severe consequence: synonymous variant
orthologous variants: 40412943-G-T