134773487-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127617457-G-C

134773607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127617831-G-A

134773668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 127617889-A-G

134773897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127618090-G-A

134774000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127618187-A-G

134774427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127621217-C-T

http://identifiers.org/hco/2/GRCh38#134780182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127623066-C-A

134780841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127623396-T-C

134782741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127624288-A-G

134782879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 127624401-G-A

134783048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127624553-G-A

134783085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127624581-G-A

http://identifiers.org/hco/2/GRCh38#134790244-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127633174-C-A

134790244-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127633174-C-G

http://identifiers.org/hco/2/GRCh38#134790331-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127633298-A-C

134790396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127633457-C-T

134790489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127633544-T-C

134792034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127633715-G-A

134792383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127634276-G-A

134819419-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 127644299-T-A

http://identifiers.org/hco/2/GRCh38#134819550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#127644458-C-A

134819781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127644964-A-G

134819980-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127645141-T-G

134821207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127645548-A-G

134821293-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127645614-T-A

134821363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127645688-G-A

134821363-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127645688-G-C

134821475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127645744-C-T

134821852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127648347-T-C

134822169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127649470-G-A

134822991-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127649958-C-G

134824237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127653143-A-G

http://identifiers.org/hco/2/GRCh38#134837413-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127654342-A-C

134837616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127654549-T-C

134837642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127654573-A-G

134838406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127656978-A-G

134838406-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127656978-A-T

134838532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127657068-T-C

http://identifiers.org/hco/2/GRCh38#134838562-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127657096-A-C

134838562-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127657096-A-T

134838568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127657102-T-C

134838807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127657344-T-C

134838820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127657359-A-G

134838820-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127657359-A-T

134838850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127657388-G-A

134838850-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127657388-G-C

134838850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127657388-G-T

http://identifiers.org/hco/2/GRCh38#134838851-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127657389-A-C

134838974-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127657519-T-G

134839595-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127658603-G-C

134839663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127658884-T-C

134839864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127659053-T-C

134841556-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 127665363-C-G

134841556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 127665363-C-T

134841692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 127665500-T-C

134841812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 127665583-A-G

134841947-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 127665694-G-C

134845244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 127666299-C-T

134845256-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 127666311-G-C

http://identifiers.org/hco/2/GRCh38#134845323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127666375-C-A

134845323-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127666375-C-G

134845323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127666375-C-T

134858815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127666738-C-T

134858905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127666819-A-G

134858906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127666820-T-C

134859385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127667803-G-A

134859470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127667896-G-A

http://identifiers.org/hco/2/GRCh38#134859509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127667934-C-A

http://identifiers.org/hco/2/GRCh38#134859512-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127667937-C-A

http://identifiers.org/hco/2/GRCh38#134859523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127667948-C-A

134859523-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127667948-C-G

134859523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127667948-C-T

134859591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127668000-T-C

134859610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127668018-A-G

134861292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127669289-T-C

134861652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127673050-T-C

134861653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127673051-G-A

134861827-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127673395-A-T

134861835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127673404-G-A

134861835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127673404-G-T

134861851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127673420-G-A

134861851-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127673420-G-C

134861857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127673426-G-A

134861857-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127673426-G-C

134861868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127673435-G-A

134861868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127673435-G-T

134861876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127673443-G-A

134861879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127673446-G-A

134861892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127673456-C-T

http://identifiers.org/hco/2/GRCh38#134861975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#127673519-C-A

134861975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 127673519-C-T

134862098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127673634-T-C

134862106-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127673642-C-G

134862144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127673680-T-C

134862936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127676307-G-A

134862955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127676326-G-A

134862955-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127676326-G-T

http://identifiers.org/hco/2/GRCh38#134863080-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127676424-C-A

134863080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127676424-C-T

http://identifiers.org/hco/2/GRCh38#134863105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127676449-C-A

134863137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127676477-T-C

http://identifiers.org/hco/2/GRCh38#134863312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127676647-C-A

134863319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127676654-G-A

134863321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127676656-G-A

134863321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127676656-G-T

134863322-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127676657-G-T

134863348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127676683-G-A

134863366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127676700-T-C

134863454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 127676785-C-T

134863462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 127676793-G-A

134863493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 127676824-G-A

134863520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 127676851-G-A

134863520-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 127676851-G-T

134863544-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 127676875-G-C

134863544-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 127676875-G-T

134863565-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 127676896-G-C

http://identifiers.org/hco/2/GRCh38#134863680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127677017-C-A

134863680-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127677017-C-G

134863680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127677017-C-T

134863719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127677037-G-A

http://identifiers.org/hco/2/GRCh38#134863725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127677043-C-A

134863725-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127677043-C-G

134863729-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127677047-T-A

http://identifiers.org/hco/2/GRCh38#134863751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127677074-C-A

134863751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127677074-C-T

134863776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127677097-T-C

134863780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127677101-G-A

134863780-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127677101-G-T

http://identifiers.org/hco/2/GRCh38#134864347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127677379-C-A

134864347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127677379-C-T

http://identifiers.org/hco/2/GRCh38#134864900-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127677855-C-A

134864900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127677855-C-T

134865248-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127678187-C-G

134865479-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127678417-C-G

134865486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127678424-G-A

134865486-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127678424-G-C

http://identifiers.org/hco/2/GRCh38#134865950-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127678920-A-C

http://identifiers.org/hco/2/GRCh38#134866411-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127679683-C-A

134866509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127679773-C-T

http://identifiers.org/hco/2/GRCh38#134866683-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127679919-C-A

134866691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127679927-T-C

134866837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127680331-G-T

http://identifiers.org/hco/2/GRCh38#134867188-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127680823-A-C

134867194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127680829-A-G

134867194-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127680829-A-T

http://identifiers.org/hco/2/GRCh38#134867198-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127680833-A-C

134867198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127680833-A-G

134867259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127680879-G-T

http://identifiers.org/hco/2/GRCh38#134867338-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127681347-C-A

134867414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127681393-G-T

134867425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127681404-T-C

134867432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127681411-T-C

134867503-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127681486-T-A

134867580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 127681526-C-T

134867584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 127681530-C-T

134867716-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127681662-G-C

134867722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127681668-C-T

134867780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127681719-T-C

134867794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127681733-A-G

134867794-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127681733-A-T

http://identifiers.org/hco/2/GRCh38#134867796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127681735-C-A

134867796-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127681735-C-G

134870231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127682937-C-T

134870783-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127685540-C-G

134870927-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127685687-T-G

134871011-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 127685787-T-A

134871011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 127685787-T-C

http://identifiers.org/hco/2/GRCh38#134871068-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127685844-C-A

134871094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127685866-G-A

134871199-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127685953-T-C

134871210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127685964-G-A

134872684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127687598-T-C

134872693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127687607-A-G

http://identifiers.org/hco/2/GRCh38#134872695-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#127687609-C-A

134883410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127689283-A-G

134884010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127689928-T-C

134898226-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127693506-A-T

134898290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127693566-G-A

134898290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127693566-G-T

134898326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127693601-T-C

134901815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 127694037-C-T

http://identifiers.org/hco/2/GRCh38#134901861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#127694083-C-A

134901861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 127694083-C-T

134902091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127694391-A-G

134902099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127694400-G-A

134902163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127694471-T-C

134902386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127694677-C-T

134902750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127695393-T-C

134902857-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127695519-T-A

134902857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127695519-T-C

134903694-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127699285-A-T

134917387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127700249-A-G

134918235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 127701403-G-A

134918235-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 127701403-G-T

http://identifiers.org/hco/2/GRCh38#134918265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#127701431-C-A

http://identifiers.org/hco/2/GRCh38#134918323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#127701488-C-A

134918349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 127701512-T-C

http://identifiers.org/hco/2/GRCh38#134918401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#127701561-C-A

134918401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 127701561-C-T

http://identifiers.org/hco/2/GRCh38#134918435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#127701594-C-A

134918435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 127701594-C-T

http://identifiers.org/hco/2/GRCh38#134918436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#127701595-C-A

134918436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 127701595-C-T

http://identifiers.org/hco/2/GRCh38#134918488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#127701604-C-A

134918488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 127701604-C-T

http://identifiers.org/hco/2/GRCh38#134918489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#127701605-C-A

134918489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 127701605-C-T

134918501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 127701617-C-T

http://identifiers.org/hco/2/GRCh38#134918598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#127701698-C-A

134918598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40130
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 127701698-C-T