http://identifiers.org/hco/11/GRCh38#134332007-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#26717731-C-A

134332007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 26717731-C-T

http://identifiers.org/hco/11/GRCh38#134332089-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#26717650-C-A

134332089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 26717650-C-T

134332105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 26717634-G-A

134332105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 26717634-G-T

http://identifiers.org/hco/11/GRCh38#134332110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#26717629-C-A

134332110-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 26717629-C-G

134332110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 26717629-C-T

http://identifiers.org/hco/11/GRCh38#134332202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26717539-C-A

134332202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26717539-C-T

http://identifiers.org/hco/11/GRCh38#134332224-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26717516-C-A

134332224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26717516-C-T

http://identifiers.org/hco/11/GRCh38#134332291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26717472-C-A

134332291-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26717472-C-G

134332291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26717472-C-T

134332537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26717236-C-T

134332851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26716982-C-T

134332985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26716821-T-C

134333240-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26716594-T-A

134333250-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26716584-G-C

134333306-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26716526-G-C

134333910-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26716044-T-G

134334046-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26715922-G-T

134334322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26715658-T-C

134334646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26715401-C-T

134334836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26715226-C-T

134334991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26715079-C-T

134335072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26714937-G-A

134335072-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26714937-G-C

134335099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26714910-G-A

134335353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26714712-T-C

134335402-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26714663-G-C

http://identifiers.org/hco/11/GRCh38#134335476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26714591-C-A

134336762-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26713285-A-T

http://identifiers.org/hco/11/GRCh38#134336825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26713234-C-A

134337092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26712961-T-C

134337794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26712588-G-A

134337826-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26712549-T-G

134337957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26712434-G-A

134338184-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26712241-G-C

134338211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26712212-A-G

http://identifiers.org/hco/11/GRCh38#134338470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26711926-C-A

134338565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26711852-T-C

134338675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26711743-C-T

134338789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26711644-G-A

134338798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26711635-G-T

134339158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26711253-G-A

134339362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26711044-C-T

134339453-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26710950-T-G

134339460-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26710943-A-T

134339478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26710925-T-C

134339482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26710921-C-T

134339633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26710780-A-G

134339633-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26710780-A-T

134340930-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26709585-C-G

134341038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26709484-T-C

134341201-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26709372-C-G

134341201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26709372-C-T

134341251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26709324-G-A

134341251-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26709324-G-C

134341326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26709251-A-G

134341334-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26709243-T-G

134341350-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26709232-C-G

134341384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26709198-G-A

134341867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26708787-G-A

134341867-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26708787-G-C

134342207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26708502-G-A

134342553-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26708127-G-T

134342671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26707998-G-A

134342671-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26707998-G-T

134342701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26707949-G-A

134342701-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26707949-G-C

134342701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26707949-G-T

134342789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26707862-G-A

134342789-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26707862-G-T

134342790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 26707861-C-T

134342958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 26707693-G-A

134342958-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 26707693-G-C

134342972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26707677-C-T

134344136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26706386-G-A

134344179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26706343-A-G

http://identifiers.org/hco/11/GRCh38#134344297-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26706212-A-C

134344297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26706212-A-G

http://identifiers.org/hco/11/GRCh38#134344442-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26706093-A-C

134344460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26706075-G-A

134344514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26706030-G-T

134344521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26706023-A-G

134344548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26705973-G-A

134344548-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26705973-G-C

134344548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26705973-G-T

134344560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26705962-G-A

134344560-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26705962-G-C

134344560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26705962-G-T

134344596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26705923-A-G

134344627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26705892-C-T

134344656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26705864-G-A

134344682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26705840-G-A

134344686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26705836-G-A

134344846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26705716-T-C

134344911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26705627-G-A

134344911-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26705627-G-C

134344911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26705627-G-T

http://identifiers.org/hco/11/GRCh38#134344937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26705603-C-A

134345140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26705365-T-C

134345168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26705331-A-G

http://identifiers.org/hco/11/GRCh38#134345235-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26705291-C-A

134345235-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26705291-C-G

http://identifiers.org/hco/11/GRCh38#134345240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26705286-C-A

134345240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26705286-C-T

134345256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26705270-T-C

134345316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26705212-G-A

134345508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26705006-G-A

134345508-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26705006-G-T

134345538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26704976-T-C

134346178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26704380-C-T

134346441-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26704138-T-A

134346454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26704125-T-C

134346562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26704033-A-G

134346599-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26704000-T-G

http://identifiers.org/hco/11/GRCh38#134346635-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26703961-C-A

134346635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26703961-C-T

134346675-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26703921-T-A

134346675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26703921-T-C

134346722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26703878-C-T

134346771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26703830-T-C

http://identifiers.org/hco/11/GRCh38#134346804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26703815-C-A

134346804-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26703815-C-G

134346804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26703815-C-T

http://identifiers.org/hco/11/GRCh38#134346886-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26703756-C-A

134346886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26703756-C-T

134346901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26703741-G-T

http://identifiers.org/hco/11/GRCh38#134346955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26703688-C-A

134346955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26703688-C-T

134346965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26703679-T-C

134346965-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26703679-T-G

http://identifiers.org/hco/11/GRCh38#134347003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26703631-C-A

134347003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26703631-C-T

http://identifiers.org/hco/11/GRCh38#134347022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26703582-C-A

http://identifiers.org/hco/11/GRCh38#134347100-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26703428-C-A

134347100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26703428-C-T

134347101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26703427-C-T

134347123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26703408-G-A

134347123-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26703408-G-T

134347160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26703376-A-G

http://identifiers.org/hco/11/GRCh38#134347163-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26703373-C-A

134347163-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26703373-C-G

134347163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26703373-C-T

http://identifiers.org/hco/11/GRCh38#134347180-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26703357-C-A

134347180-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26703357-C-G

134347180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26703357-C-T

134347265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26703245-T-C

134347309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26703201-C-T

134347505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26703005-C-T

134347744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26702805-A-G

134347920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26702651-A-G

134347921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26702650-T-C

134348208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26702343-T-C

134355023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26693234-C-T

134355052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26693198-C-T

134355120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26693132-A-G

134355275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26692985-C-T

http://identifiers.org/hco/11/GRCh38#134355300-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26692966-A-C

134355427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26692866-A-G

134355823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26692504-T-C

134355823-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26692504-T-G

http://identifiers.org/hco/11/GRCh38#134355904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26692455-C-A

134355918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26692441-G-A

134355984-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26692373-G-C

http://identifiers.org/hco/11/GRCh38#134356106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26692263-C-A

134356106-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26692263-C-G

134356106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26692263-C-T

134356112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26692257-T-C

134356112-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26692257-T-G

http://identifiers.org/hco/11/GRCh38#134356130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26692243-C-A

134356130-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26692243-C-G

134356131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26692242-A-G

134356169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26692202-A-G

134356190-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26692164-T-G

134356195-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26692159-G-T

http://identifiers.org/hco/11/GRCh38#134356220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26692134-C-A

http://identifiers.org/hco/11/GRCh38#134356261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26692096-C-A

http://identifiers.org/hco/11/GRCh38#134356270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26692087-C-A

134356270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26692087-C-T

134356409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26691952-G-A

134356542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26691816-A-G

134356547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26691811-G-T

134356685-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26691674-T-A

134356909-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26691458-C-G

134356989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26691378-A-G

134357004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26691364-T-C

134357039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26691337-G-A

134357094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26691276-A-G

134357144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26691228-G-A

134357144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26691228-G-T

134357259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26691114-G-A

134357534-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26690847-C-G

134357694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26690672-G-A

134357941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26690396-A-G

134358069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26690256-C-T

http://identifiers.org/hco/11/GRCh38#134358134-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26690208-A-C

134358135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26690207-T-C

134358261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26690110-T-C

134358439-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26689941-C-G

134358439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26689941-C-T

134358455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26689925-G-A

134358455-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26689925-G-T

134358549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26689851-C-T

134358550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26689850-G-A

134358550-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26689850-G-T

134358579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26689825-T-C

134358909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26689520-G-A

134358909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26689520-G-T

134358930-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26689517-G-T

134358989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26689465-T-C

134358989-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26689465-T-G

http://identifiers.org/hco/11/GRCh38#134359004-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26689452-C-A

134359012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26689444-G-A

134359014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26689442-T-C

134359129-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26689325-A-T

134359132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26689322-G-A

134359132-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26689322-G-T

134359817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26688279-G-A

134359817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26688279-G-T

http://identifiers.org/hco/11/GRCh38#134359818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26688278-C-A

134359818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26688278-C-T

134359848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26688245-T-C

http://identifiers.org/hco/11/GRCh38#134359864-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26688226-C-A

134359870-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 26688220-T-G

134359878-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26688212-T-A

134360039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26688056-T-C

134360045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 26688050-T-C

134360056-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 26688038-G-T

134360072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26688022-G-A

134360072-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26688022-G-T

http://identifiers.org/hco/11/GRCh38#134360074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26688020-C-A

134360074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26688020-C-T

134360075-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26688019-T-A

134360075-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26688019-T-G

134360105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26687987-G-A

134360124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26687968-T-C

134360125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26687967-G-A

134360132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26687960-G-A

http://identifiers.org/hco/11/GRCh38#134360142-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26687953-C-A

134360142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26687953-C-T

http://identifiers.org/hco/11/GRCh38#134360293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26687805-C-A

134360293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26687805-C-T

134360297-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 26687801-T-G

134360329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 26687764-T-C

134360394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 26687698-A-G

http://identifiers.org/hco/11/GRCh38#134360423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#26687669-C-A

134360438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 26687654-G-A

134360438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 26687654-G-T

134360660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 26687497-C-T

http://identifiers.org/hco/11/GRCh38#134360854-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26687292-C-A

134360862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26687284-G-A

http://identifiers.org/hco/11/GRCh38#134361515-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: -C-A

134361515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: -C-T

http://identifiers.org/hco/11/GRCh38#134361552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-A

http://identifiers.org/hco/11/GRCh38#134361564-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-A

http://identifiers.org/hco/11/GRCh38#134361585-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-A

134361585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

http://identifiers.org/hco/11/GRCh38#134361600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-A

134361600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

134362700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26686531-G-A

http://identifiers.org/hco/11/GRCh38#134362756-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26686482-C-A

134362809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26686411-G-A

134362809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26686411-G-T

134363002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26686255-C-T

134363003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26686254-C-T

134363077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26686182-G-A

134363077-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26686182-G-C

134363077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26686182-G-T

134363450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26685928-T-C

134363450-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26685928-T-G

134363460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26685918-G-A

134363485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26685893-G-A

134363502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26685875-G-A

134363503-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26685874-G-T

134363561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26685817-T-C

134363598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26685781-G-A

134363647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26685734-G-A

134363753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26685610-G-A

134364242-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26685419-T-G

http://identifiers.org/hco/11/GRCh38#134364267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26685398-C-A

134364267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26685398-C-T

134364311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26685352-C-T

134364425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26685240-G-A

134364425-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26685240-G-C

134364522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26685154-G-A

134364522-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26685154-G-C

134364522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26685154-G-T

http://identifiers.org/hco/11/GRCh38#134364530-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26685146-C-A

http://identifiers.org/hco/11/GRCh38#134364550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26685130-C-A

134364550-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26685130-C-G

134364550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26685130-C-T

134364554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26685126-G-A

134364554-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26685126-G-C

134364554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26685126-G-T

http://identifiers.org/hco/11/GRCh38#134364570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26685102-C-A

134364570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26685102-C-T

http://identifiers.org/hco/11/GRCh38#134364614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26685056-C-A

134364614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26685056-C-T

134364627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26685043-G-T

http://identifiers.org/hco/11/GRCh38#134364743-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26684943-C-A

134364743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26684943-C-T

134364770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26684916-C-T

134364871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26684817-G-A

134364871-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26684817-G-T

134364967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26684730-G-A

134364967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26684730-G-T

http://identifiers.org/hco/11/GRCh38#134365059-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26684637-A-C

134365059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26684637-A-G

134365064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26684632-G-A

134365064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26684632-G-T

134365118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26684574-G-T

134365211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26684437-G-T

134365255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26684393-G-A

http://identifiers.org/hco/11/GRCh38#134365676-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26683879-C-A

134365676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26683879-C-T

134365736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26683824-G-A

134365964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26683654-C-T

134366167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26683465-A-G

134366167-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26683465-A-T

134366296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26683348-C-T

134366441-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26683212-G-C

134366517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26683137-A-G

134366840-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26682824-G-C

http://identifiers.org/hco/11/GRCh38#134367005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26682596-C-A

http://identifiers.org/hco/11/GRCh38#134367015-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26682594-C-A

134367015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26682594-C-T

134367021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26682588-G-A

134367021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26682588-G-T

134367062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26682542-C-T

134367079-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26682534-G-T

134367087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26682531-G-T

http://identifiers.org/hco/11/GRCh38#134367102-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26682523-C-A

134367102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26682523-C-T

134367109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26682516-G-A

134367109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26682516-G-T

134367138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 26682487-G-T

134367144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26682481-G-A

134367144-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26682481-G-C

134367144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26682481-G-T

http://identifiers.org/hco/11/GRCh38#134367149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26682476-C-A

134367174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26682461-T-C

http://identifiers.org/hco/11/GRCh38#134367175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26682460-C-A

http://identifiers.org/hco/11/GRCh38#134367380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26682279-C-A

134367417-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26682254-T-A

134367417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26682254-T-C

134367437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26682234-G-A

134367437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26682234-G-T

134367464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26682199-A-G

134367553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26682117-A-G

134367695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26681979-C-T

134367726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26681939-A-G

134367766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26681900-G-A

134367774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26681892-G-A

134367833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26681846-G-A

134367910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26681758-G-A

134367965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26681721-T-C

134368108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26681577-T-C

134368130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26681554-C-T

134368613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26681205-C-T

134368622-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26681196-C-G

134368706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26681109-C-T

134368811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26681007-G-A

134368811-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26681007-G-C

134368822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26680995-A-G

134368829-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26680988-T-A

134368829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26680988-T-C

134368833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26680984-T-C

134369141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26680655-A-G

134369185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26680597-G-A

134369709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26680516-A-G

134369735-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26680481-C-G

http://identifiers.org/hco/11/GRCh38#134369749-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26680467-C-A

http://identifiers.org/hco/11/GRCh38#134369751-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26680465-A-C

134369778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26680439-A-G

134369876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26680339-T-C

134369936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26680280-T-C

http://identifiers.org/hco/11/GRCh38#134369939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26680277-C-A

134369942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26680275-A-G

http://identifiers.org/hco/11/GRCh38#134369972-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26680244-A-C

134369978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26680238-A-G

134369978-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26680238-A-T

http://identifiers.org/hco/11/GRCh38#134369982-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26680234-C-A

134369982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26680234-C-T

134370000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26680216-G-A

134370000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26680216-G-T

134370015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26680150-G-T

134370019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26680077-A-G

134370019-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26680077-A-T

134370174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26679925-T-C

134370212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26679887-G-T

134370306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 26679806-T-C

134370412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26679700-G-A

134370435-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26679694-G-C

134370435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26679694-G-T

134370437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26679692-G-A

134370437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26679692-G-T

134370547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26679634-G-A

134370547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26679634-G-T

134370596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26679589-A-G

134370708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26679497-G-A

134370756-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26679433-G-T

134370848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26679317-C-T

http://identifiers.org/hco/11/GRCh38#134370885-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26679280-A-C

134370885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26679280-A-G

134370885-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26679280-A-T

http://identifiers.org/hco/11/GRCh38#134370924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26679234-C-A

134370924-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26679234-C-G

134370924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26679234-C-T

134371195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26678966-C-T

134371199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26678962-A-G

134371228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26678933-T-C

134371250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26678908-A-G

134371313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26678858-G-A

134371313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26678858-G-T

134371316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26678855-C-T

134371436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26678745-G-A

134371466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26678715-A-G

134371502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26678679-T-C

134371514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26678667-G-A

http://identifiers.org/hco/11/GRCh38#134371635-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26678562-C-A

134371635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26678562-C-T

134371666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26678530-G-A

http://identifiers.org/hco/11/GRCh38#134371691-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26678510-C-A

134371720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26678482-G-A

http://identifiers.org/hco/11/GRCh38#134371760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26678441-C-A

134371760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 26678441-C-T

134371821-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26678380-C-G

134371821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 26678380-C-T

134371859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26678339-G-A

134371859-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26678339-G-C

134371860-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26678338-T-A

134371860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26678338-T-C

134371860-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26678338-T-G

134371907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26678288-G-A

134371907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26678288-G-T

134372105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26678029-C-T

134373504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26677565-T-C

http://identifiers.org/hco/11/GRCh38#134373626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26677468-C-A

http://identifiers.org/hco/11/GRCh38#134373638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26677456-C-A

134373638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26677456-C-T

http://identifiers.org/hco/11/GRCh38#134373639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26677455-C-A

134373639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26677455-C-T

http://identifiers.org/hco/11/GRCh38#134373650-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26677443-C-A

134373650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26677443-C-T

http://identifiers.org/hco/11/GRCh38#134373789-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26677298-A-C

http://identifiers.org/hco/11/GRCh38#134373832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26677264-C-A

134373846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26677250-G-A

134373846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26677250-G-T

134373919-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26677209-T-A

134373919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26677209-T-C

134373930-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26677198-G-C

134373930-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26677198-G-T

http://identifiers.org/hco/11/GRCh38#134374025-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26677115-C-A

134374040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26677100-G-A

134374040-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26677100-G-T

http://identifiers.org/hco/11/GRCh38#134374082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26677053-C-A

134374082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26677053-C-T

134374083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26677052-T-C

134374116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26677018-C-T

http://identifiers.org/hco/11/GRCh38#134374276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26676854-C-A

http://identifiers.org/hco/11/GRCh38#134374292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26676839-C-A

134374319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26676822-G-A

134374319-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26676822-G-T

http://identifiers.org/hco/11/GRCh38#134374333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26676812-C-A

134374333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26676812-C-T

http://identifiers.org/hco/11/GRCh38#134374367-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26676779-A-C

http://identifiers.org/hco/11/GRCh38#134374400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26676732-C-A

134374460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26676657-G-A

134374460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26676657-G-T

134374486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26676610-T-C

134374626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26676488-A-G

http://identifiers.org/hco/11/GRCh38#134374832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26676251-C-A

134374832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26676251-C-T

134374851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26676232-G-T

http://identifiers.org/hco/11/GRCh38#134374855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26676228-C-A

134374855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26676228-C-T

134374865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26676214-C-T

134374867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26676212-G-A

134374867-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26676212-G-T

http://identifiers.org/hco/11/GRCh38#134374879-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26676202-A-C

134374879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26676202-A-G

134374879-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26676202-A-T

134374915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26676166-T-C

134374924-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26676157-T-A

134374924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26676157-T-C

134374981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26676108-T-C

134375075-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 26676008-C-G

134375240-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 26675884-G-T

http://identifiers.org/hco/11/GRCh38#134375277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26675817-C-A

134375277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 26675817-C-T

http://identifiers.org/hco/11/GRCh38#134375281-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26675813-C-A

134375281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 26675813-C-T

134375303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 26675790-C-T

http://identifiers.org/hco/11/GRCh38#134375404-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26675692-C-A

134375404-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 26675692-C-G

134375404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 26675692-C-T

134375452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 26675641-G-A

134375452-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 26675641-G-C

134375452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 26675641-G-T

134375458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 26675635-G-A

134375458-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 26675635-G-T

134375583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 26675510-T-C

134375695-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 26675424-T-A

134375695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 26675424-T-C

134375772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26675364-T-C

http://identifiers.org/hco/11/GRCh38#134376185-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26675157-A-C

http://identifiers.org/hco/11/GRCh38#134376299-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26675076-C-A

134376299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26675076-C-T

134376354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26675029-G-A

134376354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26675029-G-T

134376435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26674998-G-A

134376639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26674818-G-A

134376670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26674787-G-A

134376722-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26674763-A-T

http://identifiers.org/hco/11/GRCh38#134376986-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26674086-C-A

134376986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26674086-C-T

134376997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26674075-G-A

134376997-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26674075-G-C

http://identifiers.org/hco/11/GRCh38#134377171-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26673882-C-A

http://identifiers.org/hco/11/GRCh38#134377199-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26673852-C-A

134377388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26673708-A-G

http://identifiers.org/hco/11/GRCh38#134377729-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26673400-C-A

134377729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26673400-C-T

134377853-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26673314-T-A

134377915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26673251-G-A

134377915-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26673251-G-C

134377930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26673236-A-G

134377960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26673219-A-G

http://identifiers.org/hco/11/GRCh38#134378045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26673113-C-A

134378045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26673113-C-T

134378051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26673107-T-C

http://identifiers.org/hco/11/GRCh38#134378121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26673030-C-A

134378121-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: non coding transcript exon variant
orthologous variants: 26673030-C-G

134378121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: non coding transcript exon variant
orthologous variants: 26673030-C-T

134378216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: non coding transcript exon variant
orthologous variants: 26672934-G-A

http://identifiers.org/hco/11/GRCh38#134378233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26672917-C-A

134378236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: non coding transcript exon variant
orthologous variants: 26672914-T-C

http://identifiers.org/hco/11/GRCh38#134378267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#26672855-C-A

134378267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: non coding transcript exon variant
orthologous variants: 26672855-C-T

134378334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: non coding transcript exon variant
orthologous variants: 26672787-T-C

134378335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25129
most severe consequence: non coding transcript exon variant
orthologous variants: 26672786-G-T