15228476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37591768-G-A

15228476-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37591768-G-T

15228595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37591661-G-A

15228595-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37591661-G-C

15228864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37591403-G-A

http://identifiers.org/hco/7/GRCh38#15229003-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37591258-A-C

15229060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37591202-C-T

15229250-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37591008-T-A

15229412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37590827-T-C

15229511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37590727-A-G

15229729-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37590554-T-A

15229729-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37590554-T-G

15229777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37590509-G-T

15229826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37590470-A-G

http://identifiers.org/hco/7/GRCh38#15230238-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37590101-A-C

15230265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37590066-T-C

http://identifiers.org/hco/7/GRCh38#15230416-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37589926-A-C

15230504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37589876-C-T

15230698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37589691-G-A

15230698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37589691-G-T

http://identifiers.org/hco/7/GRCh38#15230759-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37589637-C-A

15230759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37589637-C-T

15230771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37589625-T-C

15230817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37589603-G-T

15231337-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37589400-T-A

15231421-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37589364-C-G

15231432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37589353-T-C

http://identifiers.org/hco/7/GRCh38#15231624-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37589188-A-C

15231654-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37589158-G-C

15231716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37589096-A-G

15231832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37588982-T-C

15231897-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37588914-A-T

15231906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37588905-T-C

http://identifiers.org/hco/7/GRCh38#15231922-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37588889-C-A

15231972-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37588846-T-A

15232165-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37588476-C-G

15232191-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37588442-C-G

15232191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37588442-C-T

15232274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37588364-G-A

15232507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37588147-G-A

15232601-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37588056-A-T

15232642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37588019-C-T

15232906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37587789-G-A

15234079-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37577599-G-C

15234123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37577558-T-C

15234124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37577557-G-A

15234315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37577375-T-C

15234435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37577288-G-A

15234435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37577288-G-T

15234445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37577278-C-T

15234733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37577016-G-A

15234748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37577001-C-T

15234797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37576955-G-A

15234976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37576825-C-T

15235081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37576723-A-G

15235153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37576674-G-A

15235153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37576674-G-T

15235521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37576289-G-A

15235521-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37576289-G-C

http://identifiers.org/hco/7/GRCh38#15235638-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37575195-A-C

http://identifiers.org/hco/7/GRCh38#15235831-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37575009-A-C

http://identifiers.org/hco/7/GRCh38#15236106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37574712-C-A

15236106-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37574712-C-G

15236106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37574712-C-T

15236147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37574671-T-C

http://identifiers.org/hco/7/GRCh38#15236315-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37574173-A-C

15236315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37574173-A-G

http://identifiers.org/hco/7/GRCh38#15236317-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37574171-A-C

15236439-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37574054-G-T

15236456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37574040-T-C

15237243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37571888-T-C

15237472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37571129-T-C

http://identifiers.org/hco/7/GRCh38#15237549-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37571059-A-C

http://identifiers.org/hco/7/GRCh38#15237565-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37571043-A-C

15237602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37571006-T-C

http://identifiers.org/hco/7/GRCh38#15237616-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37570966-A-C

15237672-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37570911-T-A

15237672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37570911-T-C

http://identifiers.org/hco/7/GRCh38#15240555-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37568190-A-C

15242717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37567915-T-C

http://identifiers.org/hco/7/GRCh38#15242720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37567912-C-A

15242890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37567763-T-C

15243065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37567605-T-C

15243290-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37567406-G-C

15243719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37566735-A-G

15245209-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37558278-A-T

15245212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37558275-A-G

15245403-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37558087-G-C

15245462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37558028-G-A

15245494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37557998-T-C

15245532-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37557960-C-G

15245654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37557836-A-G

15245833-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37557645-A-T

15248679-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37554217-C-G

15248808-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37554094-C-G

http://identifiers.org/hco/7/GRCh38#15249085-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37553815-A-C

15249085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37553815-A-G

15249115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37553785-G-A

15249192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37553717-A-G

http://identifiers.org/hco/7/GRCh38#15249263-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37553647-A-C

15249494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37553433-C-T

15249496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37553431-T-C

15249598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37553330-C-T

15249925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37553036-A-G

http://identifiers.org/hco/7/GRCh38#15250162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37552801-C-A

15250162-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37552801-C-G

http://identifiers.org/hco/7/GRCh38#15250341-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37552614-A-C

15250425-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37552539-G-C

15257098-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37545242-T-A

15257098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37545242-T-C

15257098-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37545242-T-G

15257127-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37545213-A-T

15257135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37545205-T-C

15257224-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37545092-T-A

15257246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37545070-T-C

15257277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37545039-G-A

15257430-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37544897-G-T

15257469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37544878-T-C

http://identifiers.org/hco/7/GRCh38#15257507-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37544840-A-C

15257512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37544834-T-C

15257615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37544734-C-T

15257672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37544680-T-C

15257759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37544593-G-A

15257759-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37544593-G-C

15257824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37544529-T-C

http://identifiers.org/hco/7/GRCh38#15258178-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37544172-A-C

15258178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37544172-A-G

15258250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37544101-T-C

15258325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37544005-G-A

15258346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37543984-T-C

15264137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37543239-G-A

15264137-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37543239-G-T

15264336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37542993-A-G

15264514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37542820-T-C

15266463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37542738-T-C

15266530-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37542673-T-A

15266530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37542673-T-C

15266530-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37542673-T-G

15266531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37542672-G-A

15266620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37542581-T-C

15266641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37542560-G-A

15266920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37542297-G-A

http://identifiers.org/hco/7/GRCh38#15266951-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37542266-A-C

15267007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37542213-A-G

15267314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37541932-A-G

http://identifiers.org/hco/7/GRCh38#15267359-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37541890-A-C

15267431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37541815-C-T

15267524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37541727-T-C

15267632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37541621-T-C

15267749-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37541511-T-A

15267749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37541511-T-C

15267781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37541487-A-G

http://identifiers.org/hco/7/GRCh38#15267812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37541458-C-A

15267817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37541453-C-T

15267831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37541439-A-G

15267930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37541341-T-C

15267965-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37541305-T-G

15268017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37541260-T-C

15268232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37541031-T-C

15268311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37540967-T-C

15268313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37540965-A-G

15268378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37540902-T-C

15268469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37540819-A-G

15268587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37540710-A-G

15287685-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37539199-T-G

15287788-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37539097-T-A

15287804-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37539081-T-A

http://identifiers.org/hco/7/GRCh38#15287859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37539025-C-A

15287977-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37538902-G-C

15287977-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37538902-G-T

15288308-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37538798-C-G

15288310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37538796-T-C

http://identifiers.org/hco/7/GRCh38#15288597-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37538517-A-C

15288597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37538517-A-G

15288640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37538477-C-T

15288643-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37538474-A-T

http://identifiers.org/hco/7/GRCh38#15288735-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37538365-A-C

15288827-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37538277-A-T

15289180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37532819-A-G

15295598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37532749-T-C

http://identifiers.org/hco/7/GRCh38#15295610-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37532736-A-C

http://identifiers.org/hco/7/GRCh38#15296017-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37531864-C-A

15296083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37531811-G-A

15296115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37531797-T-C

15296441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37531480-C-T

15296448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37531473-G-A

15296456-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37531465-G-C

15296686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37531322-G-T

15296756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37531250-C-T

15296821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37531178-C-T

15296825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37531174-T-C

15296850-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37531149-G-C

15297006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37530989-C-T

15297007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37530988-G-A

15297007-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37530988-G-C

http://identifiers.org/hco/7/GRCh38#15297132-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37530860-C-A

15297132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37530860-C-T

http://identifiers.org/hco/7/GRCh38#15297219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37530777-C-A

15297246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37530749-C-T

15297575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37530419-G-A

15297758-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37530277-T-G

15297805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37530229-G-A

15297903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37530147-T-C

15300762-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37524106-T-G

15300981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37523911-A-G

http://identifiers.org/hco/7/GRCh38#15301540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37523677-C-A

15301563-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37523654-T-G

15301796-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37523433-T-A

15301910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37523358-A-G

15301956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37523314-T-C

http://identifiers.org/hco/7/GRCh38#15301993-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37523278-C-A

15302022-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37523247-T-G

15302036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37523233-A-G

15302240-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37523079-T-A

15302279-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37523040-T-G

15302284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37523035-C-T

15302365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37522948-T-C

http://identifiers.org/hco/7/GRCh38#15302458-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37522862-A-C

15302467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37522850-T-C

15302467-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37522850-T-G

15302599-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37522716-G-C

15302928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37522423-A-G

15302963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37522381-C-T

15302978-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37522366-T-G

15303025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37522311-T-C

15303186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37522206-T-C

http://identifiers.org/hco/7/GRCh38#15303354-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37522032-C-A

15303354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37522032-C-T

http://identifiers.org/hco/7/GRCh38#15303369-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37522014-A-C

15303569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37521818-G-A

15303595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37521792-T-C

15303647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37521740-T-C

15303648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37521739-G-A

15303947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37521484-T-C

15304183-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37521342-T-G

15304185-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37521340-C-G

15304203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37521322-A-G

15304205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37521320-T-C

15304329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37521199-C-T

15304574-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37520937-T-A

15304574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37520937-T-C

15304734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37520785-T-C

15304785-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37520742-G-C

15304821-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37520706-T-G

15304844-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37520683-T-A

15304845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37520682-T-C

15304847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37520680-T-C

15304925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37520602-A-G

15304951-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37520576-T-G

15305144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37520173-A-G

15305222-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 37520050-C-G

15305320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37519811-T-C

15305333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37519757-T-C

15305343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37519748-C-T

15305549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37519562-G-A

15305549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37519562-G-T

15305724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37519373-A-G

http://identifiers.org/hco/7/GRCh38#15306106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37519015-C-A

15306106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37519015-C-T

15306249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37518882-A-G

15306285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37518847-G-T

15306299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37518833-A-G

15306300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37518832-T-C

http://identifiers.org/hco/7/GRCh38#15306351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37518781-C-A

15306362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37518762-A-G

http://identifiers.org/hco/7/GRCh38#15306386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37518738-C-A

15306443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37518683-C-T

15306534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 37518597-T-C

http://identifiers.org/hco/7/GRCh38#15306556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37518580-C-A

15306556-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 37518580-C-G

http://identifiers.org/hco/7/GRCh38#15306641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37518501-C-A

15306744-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37518395-G-C

15306834-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37518307-T-A

15306892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37518268-T-C

15307081-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37517872-T-A

http://identifiers.org/hco/7/GRCh38#15307101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37517852-C-A

15307555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37517396-G-A

http://identifiers.org/hco/7/GRCh38#15307671-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37517290-A-C

15307671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37517290-A-G

15307731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37517224-A-G

15307731-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37517224-A-T

15307861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37517106-C-T

http://identifiers.org/hco/7/GRCh38#15307903-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37517064-A-C

15308572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37516843-T-C

15308596-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37516819-T-G

15308974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37516451-A-G

15308992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37516433-T-C

http://identifiers.org/hco/7/GRCh38#15309012-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37516413-C-A

15309150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37516277-T-C

15309217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37516212-T-C

15309432-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37516005-G-T

15309478-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37515953-A-T

15309495-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37515936-T-G

15309506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37515930-G-A

15309883-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37513723-C-G

15309944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37513667-C-T

15309984-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37513627-T-A

15309984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37513627-T-C

15310067-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37513546-C-G

15310095-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37513521-G-C

http://identifiers.org/hco/7/GRCh38#15310164-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37513452-A-C

15310260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37513352-C-T

15310684-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37512854-T-A

http://identifiers.org/hco/7/GRCh38#15310781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37512760-C-A

15310799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37512742-A-G

15310897-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37512648-C-G

15310917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37512628-G-A

15310917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37512628-G-T

15311175-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37512330-T-G

15311387-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37512166-C-G

15311648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37511930-T-C

15311668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37511910-T-C

15311798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37511789-T-C

15312075-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37511491-G-C

15312394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37511263-G-A

15313009-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37510825-T-A

15313009-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37510825-T-G

15313070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37510771-T-C

15313146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37510694-T-C

15313213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37510619-C-T

15313231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37510607-T-C

15313253-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37510593-C-G

15313487-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37510369-A-T

15314349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37510224-A-G

15314350-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37510223-T-A

15314551-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37510038-G-T

15314653-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37509938-A-T

15314742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37509840-G-A

15314762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37509820-G-A

15314762-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37509820-G-T

15314880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37509701-A-G

15314947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37509641-T-C

http://identifiers.org/hco/7/GRCh38#15314961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37509634-C-A

http://identifiers.org/hco/7/GRCh38#15315054-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37509551-A-C

15315064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37509544-G-A

15315092-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37509517-G-C

15315224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37509441-G-A

http://identifiers.org/hco/7/GRCh38#15315293-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37509380-A-C

15315317-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37509359-A-T

15315637-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37509339-A-T

15315684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37509289-T-C

15315955-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37509079-G-T

15315975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37509059-T-C

15316143-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37508895-T-G

15316144-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37508894-G-C

15316150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37508888-T-C

15316197-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37508851-A-T

15316260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37508781-G-A

15316352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37508655-T-C

15316581-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37507235-T-A

15316581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37507235-T-C

15316613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37507208-C-T

15316774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37507046-A-G

http://identifiers.org/hco/7/GRCh38#15316794-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37507026-A-C

15316906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37506918-T-C

15316981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37506850-G-A

http://identifiers.org/hco/7/GRCh38#15317275-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37506579-A-C

15317286-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37506570-G-C

http://identifiers.org/hco/7/GRCh38#15317315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37506545-C-A

15317332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37506508-G-A

15317332-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37506508-G-C

15317337-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37506503-T-A

15317349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37506491-T-C

15317635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37506200-A-G

15317658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37506177-A-G

15326041-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37501140-T-G

15326132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37501062-A-G

15326276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37500933-G-A

15326288-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37500927-T-A

15326288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37500927-T-C

15326408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37500813-T-C

15326489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37500729-A-G

15326605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37500617-G-A

15326821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37500384-A-G

15326834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37500371-G-A

15326874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37500321-A-G

15326889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37500306-A-G

15326936-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37500261-G-C

15327029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37500185-A-G

15327153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37500089-G-A

15327159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37500083-T-C

15327185-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37500057-G-C

15327208-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37500038-G-C

15327253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37499999-G-A

15327381-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37499882-T-A

15327381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37499882-T-C

15327587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37499709-G-A

15327587-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37499709-G-C

15329443-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37498989-C-G

15329470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37498974-T-C

15329692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37498761-C-T

http://identifiers.org/hco/7/GRCh38#15329700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37498753-C-A

15329870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37498591-T-C

15330128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37498071-T-C

15330128-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37498071-T-G

15330246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37497957-C-T

15330355-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37497846-T-G

15330369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37497837-T-C

http://identifiers.org/hco/7/GRCh38#15330559-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37497658-C-A

15330600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37497619-T-C

15332827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37497330-T-C

15332854-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37497304-T-A

15332854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37497304-T-C

15332975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37497182-T-C

15333233-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37496925-C-G

http://identifiers.org/hco/7/GRCh38#15333592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37496567-C-A

http://identifiers.org/hco/7/GRCh38#15333719-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37496473-A-C

15333995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37496209-C-T

15334090-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37496111-T-G

15334143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37496057-T-C

15334184-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37496015-T-A

15334277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37495933-A-G

http://identifiers.org/hco/7/GRCh38#15334663-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37495552-A-C

15334711-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37495504-T-G

15334986-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37495271-T-A

15335010-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37495248-G-C

15335010-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37495248-G-T

15335199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37495086-G-A

15335576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37494706-G-A

15335853-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37494430-A-T

15335968-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37494325-T-A

15336159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37494146-A-G

15336183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37494122-A-G

15336617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37493696-T-C

15336682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37493632-C-T

15337277-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37493065-A-T

15337409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37492945-G-A

15337474-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37492884-G-C

15337611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37492732-C-T

15337702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37492620-G-A

15337757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37492565-T-C

15337757-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37492565-T-G

15337938-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37492375-C-G

15338142-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37492152-T-A

http://identifiers.org/hco/7/GRCh38#15338267-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37492044-A-C

15338320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37491991-T-C

15338757-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37491688-T-G

15338808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37491640-A-G

15338945-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37491505-T-G

15338961-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37491490-A-T

15338968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37491483-T-C

15342108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37488938-G-A

15342121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37488925-T-C

http://identifiers.org/hco/7/GRCh38#15342165-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37488883-A-C

15342244-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37488829-A-T

15342412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37488697-A-G

15342702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37488431-A-G

15342732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37488400-A-G

http://identifiers.org/hco/7/GRCh38#15342768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37488365-C-A

15342768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37488365-C-T

15342835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37488317-G-A

15342835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37488317-G-T

http://identifiers.org/hco/7/GRCh38#15342837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37488315-C-A

15342837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37488315-C-T

15342895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37488257-G-A

15342895-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37488257-G-T

http://identifiers.org/hco/7/GRCh38#15342944-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37488201-A-C

15342960-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37488163-T-G

15343036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37488030-T-C

15343121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37487857-A-G

15343131-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37487825-G-C

15343262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37487569-T-C

15343335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37487494-T-C

15343354-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37487480-G-C

15343360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37487474-T-C

http://identifiers.org/hco/7/GRCh38#15343427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37487409-C-A

15343547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37487301-T-C

15343557-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37487291-G-C

15343560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37487288-T-C

15343668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37487179-T-C

15343669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37487178-A-G

15343675-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37487172-T-G

15343693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37487154-T-C

http://identifiers.org/hco/7/GRCh38#15343793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37487053-C-A

15343893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37486955-T-C

15343977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37486882-A-G

15344751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37486337-G-A

15344751-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37486337-G-C

15344751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37486337-G-T

15344937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37486160-G-A

15345067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37486011-G-A

15345067-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37486011-G-C

15345246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37485859-A-G

15345256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37485846-T-C

15345260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37485842-G-A

15345260-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37485842-G-T

http://identifiers.org/hco/7/GRCh38#15345271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37485828-C-A

15345294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37485810-T-C

15345297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37485807-G-A

15345312-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37485792-T-A

15345354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37485750-C-T

15345401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37485700-A-G

15345409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37485692-G-T

15345510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37485589-T-C

15345696-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37485338-C-G

15345779-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37485177-T-A

15345788-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37485169-T-A

15345828-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37485124-T-A

15345828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37485124-T-C

15345870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37485082-A-G

15345929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37485019-T-C

15346423-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37484536-G-C

15346446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37484513-G-A

15346669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37484374-T-C

15346810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37484237-T-C

15346873-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37484172-A-T

15347674-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37483372-C-G

15347690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37483356-T-C

15347717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37483328-T-C

http://identifiers.org/hco/7/GRCh38#15347760-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37483291-A-C

15348071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37482963-G-A

15348138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37482884-C-T

15348290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37482734-T-C

15348340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37482691-G-A

15348544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37482407-A-G

15348649-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37482298-T-G

15348772-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37482201-G-C

15348830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37482133-G-A

15349144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37481839-T-C

15349145-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37481838-C-G

15349239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37481755-G-A

15349239-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37481755-G-C

15349296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37481695-T-C

15349350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37481638-G-A

15349350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37481638-G-T

15350044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37479356-A-G

15350078-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37479322-G-C

15350078-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37479322-G-T

15350152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37479248-A-G

http://identifiers.org/hco/7/GRCh38#15350878-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37478497-A-C

15350878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37478497-A-G

15350996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37478410-A-G

15351191-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37478311-G-C

15351305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37478175-G-A

15351368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37478097-T-C

15351731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37477776-T-C

15351935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37477563-C-T

15352028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37477477-T-C

15352073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37477425-G-A

15352076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37477422-G-A

15352314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37477190-C-T

15352363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37477141-G-A

15352364-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37477140-C-G

15352364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37477140-C-T

15352375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37477129-A-G

15352661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37476850-G-A

15352664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37476847-A-G

15352720-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37476793-C-G

15352720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37476793-C-T

15352762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37476752-C-T

15352790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37476725-T-C

15352835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37476676-T-C

15352835-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37476676-T-G

15352863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37476649-G-A

15352863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37476649-G-T

15353190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37476345-C-T

http://identifiers.org/hco/7/GRCh38#15353777-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37475822-A-C

15353795-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37475804-C-G

15353830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37475770-G-A

15353833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37475767-G-A

15353909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37475653-C-T

15353962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37475596-C-T

15354007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37475564-G-A

15354039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37475524-A-G

15354133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37475438-G-A

15354133-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37475438-G-C

15358088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37471602-G-A

15358096-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37471594-T-A

15358096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37471594-T-C

15358111-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37471579-T-G

15358112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37471578-G-A

15358135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37471555-T-C

15358135-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37471555-T-G

15358283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37471410-G-A

15358283-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37471410-G-C

15358283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37471410-G-T

15364301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37467700-C-T

15364303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37467698-T-C

15364642-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37467356-G-C

http://identifiers.org/hco/7/GRCh38#15365520-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37464980-A-C

15365520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 37464980-A-G

15365623-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 37464877-A-T

15365631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37464868-T-C

15365666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37464834-T-C

15365666-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37464834-T-G

15365688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37464814-A-G

15365688-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37464814-A-T

15365905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37464263-G-A

15365905-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37464263-G-T

15365969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37464202-T-C

15366039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37464144-T-C

15366051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37464128-A-G

15366051-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37464128-A-T

15366115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37464088-A-G

15366264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37463960-T-C

15366274-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37463950-G-C

15366274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37463950-G-T

http://identifiers.org/hco/7/GRCh38#15366325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37463897-C-A

http://identifiers.org/hco/7/GRCh38#15366371-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37463855-A-C

15376306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37461722-G-T

http://identifiers.org/hco/7/GRCh38#15376307-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37461721-A-C

15376310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37461718-A-G

15376402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37461654-C-T

15376446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37461611-T-C

15376450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37461607-G-A

15376616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37461440-G-A

http://identifiers.org/hco/7/GRCh38#15376618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37461438-C-A

15376698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37461372-A-G

http://identifiers.org/hco/7/GRCh38#15376711-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37461359-A-C

15376800-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37461275-G-T

15377038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37461053-C-T

15377207-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37460855-C-G

http://identifiers.org/hco/7/GRCh38#15377256-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37460809-A-C

15377256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37460809-A-G

15377440-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37460640-T-G

15377474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37460607-G-T

15377678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37460406-T-C

15378058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37459767-T-C

15378225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37459639-G-A

15378225-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37459639-G-C

http://identifiers.org/hco/7/GRCh38#15378243-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37459621-A-C

15378252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37459612-T-C

15378269-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37459598-A-T

15382356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37459326-C-T

15382365-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37459311-T-G

15382443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37459234-T-C

15382458-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37459219-G-C

15382460-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37459217-G-C

15382555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37459158-A-G

15382943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37458943-T-C

15382963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37458926-A-G

http://identifiers.org/hco/7/GRCh38#15383078-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37458815-C-A

15383263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37458673-C-T

15383360-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37458611-C-G

15383451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37458534-T-C

15383540-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37458461-G-C

15384395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37457073-G-A

15384426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37457042-T-C

http://identifiers.org/hco/7/GRCh38#15384556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37456872-C-A

15384702-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37456744-T-G

15384887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37456561-G-A

15384900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37456548-T-C

15384909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37456547-G-A

15384909-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37456547-G-C

15384909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37456547-G-T

15384910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37456546-G-A

15384910-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37456546-G-T

http://identifiers.org/hco/7/GRCh38#15384913-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37456543-A-C

15384961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37456500-T-C

15384966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37456495-C-T

15384988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37456472-A-G

15385137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37456340-G-A

15385137-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37456340-G-C

15385280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37456209-A-G

15385328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37456151-A-G

http://identifiers.org/hco/7/GRCh38#15385404-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37456078-A-C

15385404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37456078-A-G

15385530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 37455949-A-G

15385530-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 37455949-A-T

15385591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37455884-A-G

15385629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37455847-A-G

15385629-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37455847-A-T

15387081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37455717-C-T

15387182-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37455627-T-A

15387298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37455522-G-A

15387298-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37455522-G-C

15387298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37455522-G-T

15387299-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37455521-A-T

15387325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37455495-A-G

15387328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37455492-A-G

15387328-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37455492-A-T

15387331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37455489-G-A

15387331-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37455489-G-C

15387331-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37455489-G-T

15387351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37455483-G-A

15387351-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37455483-G-C

15387351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37455483-G-T

15387494-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 37455354-C-G

15387630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37455214-G-A

15387630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37455214-G-T

15387635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37455209-T-C

http://identifiers.org/hco/7/GRCh38#15387650-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37455192-C-A

15387650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37455192-C-T

15387660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37455182-G-A

15387660-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37455182-G-C

15387660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37455182-G-T

http://identifiers.org/hco/7/GRCh38#15387701-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37455133-A-C

15387705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37455129-A-G

15387711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37455123-T-C

15387746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37455087-T-C

15387831-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37455008-T-G

15387835-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37455004-G-C

15388181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37454581-A-G

15388442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37454274-A-G

15388590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37454132-C-T

15388660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37454063-T-C

15388660-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37454063-T-G

15388704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37454033-G-A

15388710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37454027-T-C

15388716-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37454021-G-C

15388762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37453985-T-C

15388762-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37453985-T-G

15388810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37453947-T-C

15388833-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37453924-G-C

15388881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37453893-A-G

15389039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37453726-A-G

15389171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37453587-G-A

15389176-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37453582-G-C

15389211-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37453563-A-T

15389331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37453449-G-A

15389331-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37453449-G-C

15389650-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37453145-T-G

15389685-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37453119-T-G

15389763-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37453049-G-C

15389852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37452967-T-C

15389960-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37452860-C-G

15390019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37452801-A-G

15390143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37452677-A-G

15390573-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37452249-T-A

15390573-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37452249-T-G

15390637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37452188-T-C

15390693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 37452133-G-A

15390693-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 37452133-G-C

15390693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 37452133-G-T

15390793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37452033-A-G

15390843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 37451981-A-G

http://identifiers.org/hco/7/GRCh38#15390968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37451852-C-A

15390968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37451852-C-T

15391032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37451800-T-C

15393279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37449628-C-T

15393410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37449510-T-C

15393423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37449497-T-C

15393552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37449370-G-A

15393699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37449221-G-A

http://identifiers.org/hco/7/GRCh38#15393714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37449086-C-A

15393714-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37449086-C-G

http://identifiers.org/hco/7/GRCh38#15393732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37449068-C-A

15393732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37449068-C-T

15393771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37449032-C-T

http://identifiers.org/hco/7/GRCh38#15393797-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37449008-A-C

15393982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37448880-A-G

15393982-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37448880-A-T

15394030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37448829-T-C

15394048-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37448811-A-T

http://identifiers.org/hco/7/GRCh38#15394187-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37448679-A-C

15394187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 37448679-A-G

15394211-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37448655-T-A

15394211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37448655-T-C

15394233-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37448633-A-T

http://identifiers.org/hco/7/GRCh38#15394326-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37448564-A-C

15394326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37448564-A-G

15394456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37448460-T-C

15394465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37448451-G-A

15395326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37448251-A-G

15395339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37448241-C-T

15395407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37448164-A-G

http://identifiers.org/hco/7/GRCh38#15395440-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37448133-A-C

15395570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37448038-G-A

15395642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37447963-C-T

15395681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37447924-T-C

15395690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37447918-T-C

15395691-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37447917-C-G

15395691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37447917-C-T

15395704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37447904-T-C

15395707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37447901-T-C

15395768-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37447827-C-G

15395768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37447827-C-T

http://identifiers.org/hco/7/GRCh38#15397595-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37446866-C-A

15397691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37446738-G-A

15397865-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37446568-A-T

15398007-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37446431-T-G

15398212-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37446229-G-C

15398865-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37445563-G-C

15398878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37445550-C-T

15398906-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37445522-A-T

15399194-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37445252-A-T

15399378-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37445077-G-C

15399529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37444917-T-C

http://identifiers.org/hco/7/GRCh38#15399858-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37444489-A-C

15399858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37444489-A-G

15399872-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37444475-G-T

15400004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37444331-T-C

15400015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37444317-G-T

15400200-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37444148-G-T

http://identifiers.org/hco/7/GRCh38#15400319-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37444066-A-C

15400319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37444066-A-G

15400412-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37443994-G-C

15400454-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37443953-A-T

15400461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37443946-T-C

15400670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37443746-C-T

15401268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37443191-A-G

http://identifiers.org/hco/7/GRCh38#15401289-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37443170-C-A

15401289-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37443170-C-G

15401736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37442729-G-A

15402060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37442412-T-C

15402191-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37442291-G-C

15402191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37442291-G-T

15402295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37442211-T-C

15402365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37442140-G-T

http://identifiers.org/hco/7/GRCh38#15402877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37441751-C-A

http://identifiers.org/hco/7/GRCh38#15402927-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37441713-A-C

15403096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37441565-T-C

15403110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37441554-A-G

15403147-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37441517-T-G

15403392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37441334-T-C

15403419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37441308-C-T

15403570-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37441172-C-G

15403628-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37441115-C-G

15404110-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37440630-G-C

15404303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37440440-T-C

15404360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37440384-T-C

15404429-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37440332-T-A

15404975-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37439315-G-C

15404976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37439314-T-C

15405004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37439286-A-G

http://identifiers.org/hco/7/GRCh38#15409418-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37438983-A-C

15409432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37438969-A-G

15409487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37438916-G-A

15410638-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37437012-T-G

http://identifiers.org/hco/7/GRCh38#15410647-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37437006-C-A

http://identifiers.org/hco/7/GRCh38#15410664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37436989-C-A

15412096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37435831-C-T

15412141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37435807-T-C

http://identifiers.org/hco/7/GRCh38#15415556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37411863-C-A

http://identifiers.org/hco/7/GRCh38#15415623-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37411798-C-A

15415708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37411736-T-C

15415777-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37411683-A-T

15415877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37411610-G-T

15415910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37411577-C-T

http://identifiers.org/hco/7/GRCh38#15416877-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37409349-A-C

15417078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37409167-G-A

15417258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37408995-G-A

http://identifiers.org/hco/7/GRCh38#15417346-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37408912-A-C

15417432-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37408832-T-A

15417555-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37408708-T-A

15417555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37408708-T-C

15417773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37408501-C-T

15417787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37408483-A-G

15418362-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37407935-A-T

http://identifiers.org/hco/7/GRCh38#15418484-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37407812-C-A

15418546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37407743-A-G

15418565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 37407717-T-C

http://identifiers.org/hco/7/GRCh38#15418712-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37407574-A-C

15418712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37407574-A-G

http://identifiers.org/hco/7/GRCh38#15418740-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37407564-C-A

15418740-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37407564-C-G

15418740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37407564-C-T

15418743-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37407561-T-A

15418743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37407561-T-C

15418743-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37407561-T-G

15418777-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37407531-T-G

15419240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37407127-G-A

15419240-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37407127-G-T

http://identifiers.org/hco/7/GRCh38#15419299-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37407069-C-A

15419396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37406974-T-C

15419397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37406973-A-G

15419397-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37406973-A-T

15419430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37406935-A-G

15419503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37406867-A-G

http://identifiers.org/hco/7/GRCh38#15419511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37406859-C-A

http://identifiers.org/hco/7/GRCh38#15419559-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37406809-C-A

15420150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37406372-G-A

15420150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37406372-G-T

http://identifiers.org/hco/7/GRCh38#15420161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37406360-C-A

http://identifiers.org/hco/7/GRCh38#15420223-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37406319-A-C

15420523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37405143-A-G

15420778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37404782-G-A

15421099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37404472-G-A

15421317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37404282-T-C

http://identifiers.org/hco/7/GRCh38#15421347-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37404241-A-C

15421393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37404189-T-C

15421415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37404167-C-T

15421959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37403729-A-G

15421973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37403725-A-G

15422040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37403672-T-C

15422098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37403641-A-G

15422346-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37403489-G-C

15422483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37403378-A-G

15422483-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37403378-A-T

http://identifiers.org/hco/7/GRCh38#15422501-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37403363-A-C

15422626-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37403250-T-A

15422627-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37403249-C-G

15422709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37403163-C-T

15422720-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37403153-G-C

15422721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37403152-G-A

15422816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37403064-G-A

http://identifiers.org/hco/7/GRCh38#15422819-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37403061-A-C

15422864-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37403013-G-C

15427734-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37400444-T-A

15427734-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37400444-T-G

15428094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37400114-T-C

15428194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37400019-C-T

15428195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37400018-T-C

15428196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37400017-A-G

15428353-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37399890-G-C

15428353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37399890-G-T

15428362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37399881-C-T

http://identifiers.org/hco/7/GRCh38#15428427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37399809-C-A

15428427-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37399809-C-G

15429097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37399126-T-C

15429333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37398858-T-C

15429368-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37398820-G-C

15429462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37398715-C-T

http://identifiers.org/hco/7/GRCh38#15429589-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37398613-A-C

15429650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37398564-G-A

15429732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37398489-A-G

15430020-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37398207-A-T

15430340-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37397930-C-G

http://identifiers.org/hco/7/GRCh38#15430612-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37397700-A-C

15430612-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37397700-A-T

15430682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37397668-T-C

15430703-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37397647-T-A

15430703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37397647-T-C

15430752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37397582-C-T

15430848-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37397478-G-C

15430861-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37397465-T-G

15430961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37397403-A-G

http://identifiers.org/hco/7/GRCh38#15431155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37397209-C-A

http://identifiers.org/hco/7/GRCh38#15431216-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37397148-C-A

15431240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37397124-T-C

15431275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37397089-G-T

15431362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37397002-T-C

15431790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37396612-T-C

15432636-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37396549-C-G

15432636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37396549-C-T

15432704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37396482-A-G

15432742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37396451-G-A

15432749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37396444-C-T

http://identifiers.org/hco/7/GRCh38#15432836-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37396357-A-C

15432914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37396296-C-T

15432978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37396232-A-G

http://identifiers.org/hco/7/GRCh38#15433019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37396193-C-A

15433091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37396128-A-G

15433441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37395822-A-G

15440373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37391249-A-G

15440465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37391154-T-C

15440512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37391124-A-G

15440514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37391122-G-A

15440514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37391122-G-T

15440643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37390989-T-C

15440688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37390964-G-A

15440862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37390786-A-G

15440875-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37390776-A-T

15441001-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37390663-A-T

15441382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37390315-T-C

15441384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37390313-G-T

15441532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37390170-A-G

http://identifiers.org/hco/7/GRCh38#15441638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37390072-C-A

15441960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37389766-G-T

15443445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37389277-G-A

15443445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37389277-G-T

15443497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37389222-T-C

15443522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37389197-G-T

15443588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37389144-A-G

15443617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37389112-T-C

15444183-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37388603-A-T

15444211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37388575-C-T

15444245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37388538-T-C

15444306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37388476-C-T

15444349-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37388422-T-G

15444386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37388392-C-T

15444392-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37388386-G-T

http://identifiers.org/hco/7/GRCh38#15444406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37388372-C-A

15444487-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37388289-C-G

15444487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37388289-C-T

15444508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37388268-C-T

15444575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37388203-T-C

http://identifiers.org/hco/7/GRCh38#15444597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37388181-C-A

15444637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37388150-G-A

15445699-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37386941-T-G

15446547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37385627-A-G

15446758-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37385395-T-A

15446803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37385350-T-C

15446839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37385319-T-C

15447225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37384975-A-G

15447415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37384784-C-T

15447471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37384728-G-T

http://identifiers.org/hco/7/GRCh38#15447993-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37383538-A-C

15448109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37383412-C-T

15448156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37383371-T-C

15448169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37383362-A-G

15448431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37383157-T-C

15448485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37383104-T-C

15448591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37383006-T-C

15448602-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37382995-T-A

15448602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37382995-T-C

15448741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37382780-G-A

15449098-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37382417-G-C

15449216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37382320-A-G

15449222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37382314-G-A

15449898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37381952-T-C

15450024-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37381822-A-T

15457312-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37375112-A-T

15457395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37375039-G-A

15457404-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37375030-T-A

15457404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37375030-T-C

15458157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37374246-A-G

15458158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37374245-C-T

15458272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37374132-T-C

http://identifiers.org/hco/7/GRCh38#15458805-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37373592-A-C

15459184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37373250-G-A

15459419-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37373073-C-G

15459512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37372990-A-G

http://identifiers.org/hco/7/GRCh38#15459687-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37372336-A-C

http://identifiers.org/hco/7/GRCh38#15460080-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37371966-C-A

15460080-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37371966-C-G

15460081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37371965-A-G

15460117-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37371905-G-C

15460117-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37371905-G-T

15460131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37371889-G-T

15460805-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37371014-T-A

15460867-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37370980-A-T

15460962-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37370898-A-T

http://identifiers.org/hco/7/GRCh38#15461262-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37370638-A-C

15461500-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37367512-C-G

15461651-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 37367375-G-C

15461680-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37367345-C-G

15461775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 37367124-C-T

15461811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 37366998-G-A

15461811-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 37366998-G-C

15461896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 37366866-T-C

15461994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 37366785-A-G

15462076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 37366709-T-C

http://identifiers.org/hco/7/GRCh38#15462098-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#37366687-A-C

15462118-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 37366667-C-G

15462134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 37366651-A-G

15462240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37366546-C-T

15462314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37366460-A-G

15462408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37366366-T-C

http://identifiers.org/hco/7/GRCh38#15462410-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37366364-C-A

15462410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37366364-C-T

15462424-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37366351-G-T

15462427-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37366348-T-A

15462719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37365090-T-C

15462773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37365041-G-A

15462789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37365026-T-C

15463012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37364803-T-C

15463055-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37364756-C-G

15463055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37364756-C-T

15463605-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37364573-T-G

15463707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37364463-T-C

15466040-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37363661-G-C

15466072-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37363624-G-C

15466526-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37362333-G-C

15466539-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37362321-G-T

15466852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37362061-T-C

15466872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37362045-T-C

15466912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37362007-G-A

15467023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37361926-T-C

http://identifiers.org/hco/7/GRCh38#15467082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37361868-C-A

15467082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37361868-C-T

15467107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37361843-A-G

15467145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37361815-T-C

15467178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37361782-A-G

15467178-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37361782-A-T

15467501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37361460-T-C

15467810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37361153-A-G

15467974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37360976-C-T

15468229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37360726-T-C

15468340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37360615-G-A

15468449-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37360385-G-T

15468552-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37360310-T-G

15468723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37360238-T-C

15468789-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37360182-G-T

15468901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37360074-G-T

15469026-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37359963-A-T

http://identifiers.org/hco/7/GRCh38#15469058-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37359933-A-C

15469061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37359932-G-A

15469129-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37359870-T-G

15469138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37359861-A-G

15469509-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37359193-T-A

15469669-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37359089-T-A

15469686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37359065-T-C

15469895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37358859-G-A

15469895-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37358859-G-T

http://identifiers.org/hco/7/GRCh38#15469897-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37358857-C-A

15470082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37358624-T-C

15470619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37358132-C-T

15470668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37358115-C-T

15470677-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37358105-T-G

15470742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37358022-G-T

15470745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37358019-A-G

15470761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37358003-A-G

15470963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37357817-C-T

15471756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37357035-G-A

15471997-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37356821-C-G

15472021-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37356798-T-G

http://identifiers.org/hco/7/GRCh38#15472102-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37356717-C-A

15472178-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37356641-C-G

http://identifiers.org/hco/7/GRCh38#15472279-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37356543-A-C

http://identifiers.org/hco/7/GRCh38#15472382-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37356431-A-C

15472447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37356369-G-A

15472474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37356342-G-A

15472501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37356315-A-G

http://identifiers.org/hco/7/GRCh38#15472502-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37356314-A-C

15475950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37355283-G-A

15475950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37355283-G-T

15476005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37355247-T-C

15476142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37355140-T-C

15476290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37354928-G-A

15476451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37354790-G-A

15478310-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37353267-G-C

15478313-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37353264-T-G

15478316-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37353261-C-G

http://identifiers.org/hco/7/GRCh38#15478450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37353143-C-A

15478527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37353071-T-C

15478934-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37351422-C-G

15479044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37351323-A-G

15479121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37351270-T-C

15479138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37351261-T-C

15479294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37351107-G-A

15479547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37350879-A-G

15479741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37350691-A-G

15479768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37350670-G-T

15479803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37350635-A-G

15480206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37350257-G-A

15484129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37348997-C-T

15484237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37348898-A-G

15484330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37348818-A-G

15484475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37348676-G-A

15484625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37348541-A-G

15484642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37348528-A-G

15484924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37348303-T-C

15484973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37348255-A-G

15484976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37348252-G-A

15485573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37347965-C-T

15485639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37347903-G-A

15485775-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37347772-G-T

15485794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37347753-T-C

15485794-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37347753-T-G

15485818-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37347729-T-G

15486069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37347544-T-C

15486073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37347540-C-T

http://identifiers.org/hco/7/GRCh38#15486205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37347416-C-A

15486205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37347416-C-T

15486207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37347415-A-G

15486478-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37347177-T-G

15486568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37347085-G-A

15486618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37347039-G-A

15486696-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37346970-A-T

15486784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37346874-T-C

15486808-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37346827-T-A

15486808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37346827-T-C

15486840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37346738-G-A

15486840-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37346738-G-C

15486878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37346602-T-C

15486910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37346574-G-A

15486910-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37346574-G-C

15486963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37346522-A-G

15487053-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37346432-G-C

15487144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37346375-A-G

15487353-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37346168-G-C

15487432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37346092-T-C

15487520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37346011-T-C

15487559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37345982-A-G

15487578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37345963-C-T

15488306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37345372-T-C

15488368-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37345316-T-G

15488499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37345202-T-C

15488527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37345174-T-C

15488617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37345085-A-G

15488731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37344971-A-G

15488774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37344934-C-T

15488880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37344829-T-C

15488991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37344734-A-G

15488991-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37344734-A-T

15489033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37344704-T-C

15489285-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37344458-T-G

15489376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37344376-C-T

15489871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37343882-T-C

15489914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37343856-C-T

15489997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37343788-T-C

15490005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37343780-C-T

15490065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37343722-T-C

15490145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37343639-T-C

15490905-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37342906-T-G

15490951-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37342860-A-T

15491035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37342779-G-A

15491335-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37342506-G-C

15491622-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37342245-C-G

15491765-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37342110-C-G

15491952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37341852-T-C

15491969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37341835-C-T

15492261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37341539-G-A

15492261-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37341539-G-C

15492341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37341457-A-G

15492386-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37341425-T-A

15494067-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37335569-G-C

15494225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37335418-T-C

15495477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37334410-T-C

15495528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37334362-T-C

15495583-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37334307-T-G

15495718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37334185-C-T

15496107-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37333868-G-T

15496139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37333838-C-T

15498928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37329727-C-T

15498982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37329673-T-C

15499357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37329244-C-T

15499680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37328984-G-A

15499819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37328825-A-G

15499833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37328811-G-A

15499849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37328795-A-G

15499956-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37328737-T-A

15500016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37328678-G-T

15500054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37328641-T-C

15500140-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37328555-T-A

15500234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37328467-T-C

15500275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37328427-G-A

15501701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37325708-G-A

15501701-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37325708-G-C

15501814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37325599-A-G

15501930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37325514-T-C

15501990-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37325443-G-C

15502010-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37325424-G-T

15502034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37325401-A-G

15502107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37325333-T-C

15502178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37325239-G-A

15502516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37324868-G-T

15502535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37324851-A-G

http://identifiers.org/hco/7/GRCh38#15502597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37324791-C-A

15502597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37324791-C-T

http://identifiers.org/hco/7/GRCh38#15502870-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37324568-C-A

15502870-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37324568-C-G

15503026-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37324432-T-A

15503805-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37323444-T-A

15503806-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37323443-C-G

15504012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37323248-T-C

15504069-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37323193-C-G

15504077-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37323185-T-A

15504218-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37323089-T-G

15504350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37322976-T-C

15504407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37322919-C-T

http://identifiers.org/hco/7/GRCh38#15504740-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37322584-A-C

15504783-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37322516-A-T

http://identifiers.org/hco/7/GRCh38#15504913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37322387-C-A

15504993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37322332-C-T

15505111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37322219-T-C

http://identifiers.org/hco/7/GRCh38#15505117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37322213-C-A

15505117-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37322213-C-G

15505117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37322213-C-T

15505507-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37321890-T-A

15505652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37321759-T-C

15505652-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37321759-T-G

http://identifiers.org/hco/7/GRCh38#15506045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37321366-C-A

15506504-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37320885-T-G

http://identifiers.org/hco/7/GRCh38#15506887-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37320522-A-C

15507350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37320056-A-G

15507381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37320017-C-T

15507472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37319921-C-T

15507496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37319898-A-G

15507910-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37319569-G-C

15507910-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37319569-G-T

15507964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37319516-C-T

http://identifiers.org/hco/7/GRCh38#15508855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37318311-C-A

15508867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37318299-C-T

15508891-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37318275-G-C

15509055-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37318106-T-G

15509090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37318080-C-T

http://identifiers.org/hco/7/GRCh38#15509234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37317946-C-A

15509242-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37317938-C-G

15509495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37317720-T-C

15509521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37317695-T-C

15509521-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37317695-T-G

15509559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37317656-G-T

15509602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37317611-G-A

15509716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37317448-A-G

15509751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37317411-G-A

15510020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37317219-T-C

15510099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37317148-G-A

15511659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37316377-A-G

15511669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37316367-A-G

15511670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37316366-T-C

15511975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37316181-G-A

15512003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37316144-G-A

http://identifiers.org/hco/7/GRCh38#15512018-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37316129-A-C

15512132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37315989-C-T

15514224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37315170-T-C

15514322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37315072-C-T

15514323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37315071-G-A

15514612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37314805-G-A

15514990-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37314359-T-G

15515020-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37314331-T-G

15515274-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37314093-C-G

15515552-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37313763-A-T

15515591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37313653-A-G

15515657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37313547-T-C

15516149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37313038-C-T

15516740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37312510-G-A

15516740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37312510-G-T

15516881-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37312364-G-C

15517080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37312179-T-C

15532627-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37309208-T-A

15533827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37308230-A-G

15534245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37307909-G-A

15534475-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37307722-T-A

15541905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37304787-T-C

15542280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37304437-G-A

15542468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37304253-A-G

15542950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37303715-C-T

15543041-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37303616-T-A

15543120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37303541-A-G

15543128-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37303533-T-G

15543158-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37303412-C-G

15543158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37303412-C-T

15543243-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37303282-G-C

15543389-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37303135-T-A

15543400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37303124-A-G

http://identifiers.org/hco/7/GRCh38#15543424-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37303101-C-A

15543578-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37302944-T-C

15543650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37302872-G-A

http://identifiers.org/hco/7/GRCh38#15544625-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37302715-A-C

15544642-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37302698-A-T

15544689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37302652-T-C

15544716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37302625-T-C

15544716-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37302625-T-G

15544822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 37302521-G-A

15544822-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 37302521-G-T

http://identifiers.org/hco/7/GRCh38#15544831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37302512-C-A

15544837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 37302506-C-T

15544839-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 37302504-T-A

15544839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 37302504-T-C

http://identifiers.org/hco/7/GRCh38#15544867-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37302476-C-A

15544867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 37302476-C-T

http://identifiers.org/hco/7/GRCh38#15544984-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37302360-A-C

15544995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37302349-T-C

15545006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37302338-A-G

15545035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37302306-T-C

15545036-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37302305-C-G

http://identifiers.org/hco/7/GRCh38#15545046-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37302295-C-A

15545049-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37302292-T-A

15545055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37302286-T-C

15545055-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37302286-T-G

http://identifiers.org/hco/7/GRCh38#15545059-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37302274-A-C

15545059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37302274-A-G

15545059-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37302274-A-T

15545061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37302272-G-T

15545065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37302268-T-C

15545092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37302239-T-C

15545356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37302013-G-T

15545404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37301967-T-C

15545495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37301893-T-C

15545538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37301862-T-C

15545559-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37301841-T-A

15545651-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37301748-T-G

15553587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37300400-A-G

15553851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37300187-C-T

15554130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37299911-G-A

15554162-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37299879-C-G

15554247-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37299797-T-C

15554481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37299564-G-A

15554523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37299520-C-T

http://identifiers.org/hco/7/GRCh38#15555306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37299357-C-A

15555306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37299357-C-T

15555356-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37299292-G-C

15555372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37299276-G-A

15555372-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37299276-G-T

15555515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37299128-C-T

15555520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37299122-A-G

15555568-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37299075-T-A

15555631-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 37299020-T-A

15555631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 37299020-T-C

15556263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37298788-T-C

15556333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37298718-G-A

http://identifiers.org/hco/7/GRCh38#15556413-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37298643-A-C

15556497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37298559-T-C

15556505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37298551-A-G

15556565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37298491-T-C

http://identifiers.org/hco/7/GRCh38#15556645-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37298409-A-C

15556645-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37298409-A-T

15556708-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37298356-T-A

15556915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37298123-A-G

15557085-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37297955-C-G

15557085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37297955-C-T

15557176-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37297867-C-G

15557176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37297867-C-T

15557196-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37297847-T-A

15557204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37297839-T-C

15557691-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37297379-C-G

http://identifiers.org/hco/7/GRCh38#15557896-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37297196-C-A

15557959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37297160-T-C

15558349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37295684-C-T

15558366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37295667-G-A

15558366-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37295667-G-T

15558544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37295483-T-C

15558582-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37295446-T-G

15558747-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37295305-T-A

15558793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37295258-T-C

15558815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37295233-G-T

15558848-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37295204-T-A

15559004-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37295053-C-G

15559040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37295019-G-A

15559047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37295012-A-G

15559065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37294990-G-A

15559065-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37294990-G-T

15559070-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37294985-T-G

15559237-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37294826-G-T

15559449-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37294630-G-C

15559638-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37294483-T-A

15559668-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37294453-T-G

15559874-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37294293-G-C

15559874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37294293-G-T

15559904-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37294263-A-T

15560001-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37293969-A-T

15560016-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37293954-A-T

15560020-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37293950-A-T

http://identifiers.org/hco/7/GRCh38#15560021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37293949-C-A

http://identifiers.org/hco/7/GRCh38#15560061-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37293906-C-A

15560061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37293906-C-T

15560131-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37293843-T-A

15560131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37293843-T-C

http://identifiers.org/hco/7/GRCh38#15560132-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#37293842-C-A

15560183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 37293791-G-T

15560308-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37293666-T-A

15560308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37293666-T-C

15560383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37293601-G-A

15560404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37293582-T-C

15560418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37293568-C-T

15560530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37293456-T-C

15560675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37293311-A-G

15560923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37292910-A-G

15561282-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37292581-A-T

15561336-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37292528-G-T

15561337-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37292527-T-A

15561916-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33784
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37291969-G-C