163161773-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 169510483-G-T

163161787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 169510469-T-C

163161787-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 169510469-T-G

http://identifiers.org/hco/1/GRCh38#163161794-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169510462-C-A

163161834-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 169510448-G-T

163161842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 169510440-G-A

163161870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169510420-C-T

http://identifiers.org/hco/1/GRCh38#163161877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169510413-C-A

163161877-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169510413-C-G

163161877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169510413-C-T

163162005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169510293-G-A

163162005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169510293-G-T

163162020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169510278-G-A

163162020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169510278-G-T

163162053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169510246-C-T

163162089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169510213-T-C

163162103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169510199-A-G

163162103-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169510199-A-T

163162258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169510057-G-T

163162420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169509898-T-C

163162520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169509798-T-C

163162531-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169509758-T-G

163162580-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169509714-A-T

163162643-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169509663-T-A

163162643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169509663-T-C

163162684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169509633-T-C

163162684-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169509633-T-G

163162690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169509627-A-G

163162772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169509525-T-C

http://identifiers.org/hco/1/GRCh38#163162783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169509514-C-A

163162783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 169509514-C-T

http://identifiers.org/hco/1/GRCh38#163162832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#169509501-C-A

163162879-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169509454-G-T

http://identifiers.org/hco/1/GRCh38#163162927-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169509406-A-C

163163261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169509108-T-C

163163271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169509098-T-C

163163384-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169508985-T-A

163163590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169508785-C-T

163163604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169508771-T-C

163163817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169508594-G-T

163163823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169508588-C-T

163164103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169508309-C-T

163164276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169508137-G-T

163164540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169507874-C-T

163165017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169507228-T-C

163165112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169507161-G-A

163165286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169507002-C-T

163165898-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169506708-T-G

http://identifiers.org/hco/1/GRCh38#163165927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169506686-C-A

163165998-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169506625-G-C

163166301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169506359-G-A

163166615-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169506092-C-G

163166943-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169505752-G-C

163166973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169505722-C-T

163167100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 169505596-T-C

163167410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169505303-A-G

163167464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169505258-G-A

163167523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169505214-T-C

163167548-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169505190-T-C

163167565-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169505173-T-A

163167603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169505134-G-A

163167648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169505081-G-A

163167801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169504923-A-G

163168029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 169504719-T-C

163168038-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 169504710-T-A

163168261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 169504501-T-C

163168413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 169504351-T-C

163168493-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 169504269-T-G

163168678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169504045-C-T

163168810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169503921-G-A

163168868-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169503869-T-A

163169907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169503674-A-G

http://identifiers.org/hco/1/GRCh38#163169945-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169503642-A-C

163169945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169503642-A-G

163170527-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169502604-G-T

http://identifiers.org/hco/1/GRCh38#163170765-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169502374-A-C

http://identifiers.org/hco/1/GRCh38#163170834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169502301-C-A

163170834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169502301-C-T

163170835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169502300-G-A

163170887-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169502236-G-C

163171134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169502030-G-T

163171203-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169501974-T-A

163171324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169501846-G-A

163171528-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169501669-G-T

163171675-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169501511-T-A

163171845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169501365-C-T

163171860-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169501350-G-C

163171904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169501337-A-G

163171906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169501335-A-G

163172012-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169501231-C-G

163172326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169500904-T-C

http://identifiers.org/hco/1/GRCh38#163172336-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169500890-A-C

163172336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169500890-A-G

http://identifiers.org/hco/1/GRCh38#163172359-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169500868-C-A

http://identifiers.org/hco/1/GRCh38#163172429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169500774-C-A

163172429-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169500774-C-G

163172429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169500774-C-T

http://identifiers.org/hco/1/GRCh38#163172446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169500757-C-A

163172446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169500757-C-T

http://identifiers.org/hco/1/GRCh38#163172457-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169500746-C-A

163172470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169500733-T-C

163172472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169500731-T-C

163172473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169500730-T-C

163172647-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169500303-T-A

163172647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169500303-T-C

163172671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169500276-A-G

163172671-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169500276-A-T

http://identifiers.org/hco/1/GRCh38#163172674-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169500273-C-A

163172674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169500273-C-T

163172686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169500261-G-A

163172686-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169500261-G-C

163172862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169500101-A-G

163172996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169499918-C-T

163173011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169499910-A-G

163173167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169499753-T-C

163173399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169499548-G-A

163173399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169499548-G-T

163173497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169499453-G-A

163173706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169499236-A-G

163174583-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169498917-G-C

163174583-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169498917-G-T

163174725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: -A-G

163174823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169498568-C-T

163174841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169498550-T-C

163174997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 169498391-G-A

163175115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169498284-T-C

163175709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169497976-T-C

163175841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

163175914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169497795-G-A

163175914-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169497795-G-T

163176766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169496889-C-T

163177267-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169496485-T-A

http://identifiers.org/hco/1/GRCh38#163177324-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169496428-A-C

163177390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169496363-T-C

http://identifiers.org/hco/1/GRCh38#163178388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169495632-C-A

163178388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169495632-C-T

163178545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169495471-C-T

163178579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169495446-T-C

163178603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169495417-T-C

163178994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169495033-C-T

http://identifiers.org/hco/1/GRCh38#163179024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169495002-C-A

163179142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169494893-T-C

163179922-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169494227-T-G

163180308-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169494121-T-A

163180363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169494051-G-A

163181239-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169493909-T-A

163181251-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169493897-C-G

163182092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169493536-T-C

163182264-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169493338-T-G

163182442-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169493183-G-C

163182654-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169492972-T-G

163182689-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169492937-G-C

163182852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169492787-G-A

163182944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169492699-G-A

163182944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169492699-G-T

http://identifiers.org/hco/1/GRCh38#163183019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169492621-C-A

163183402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169492168-T-C

163183606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169491988-T-C

163183616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169491979-G-A

163183655-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169491941-T-G

163183791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169491649-C-T

http://identifiers.org/hco/1/GRCh38#163183839-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169491611-C-A

163183839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169491611-C-T

163184058-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169491472-G-T

http://identifiers.org/hco/1/GRCh38#163184390-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169491151-C-A

163184439-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169491113-T-A

163184514-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169490995-T-A

163184559-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169490957-G-C

163184834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169490719-G-A

163184984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169490569-A-G

163192653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169489666-T-C

163192718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169489620-G-A

163192865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169489513-A-G

163193112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169489262-T-C

163193135-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169489201-G-C

163193310-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169489005-C-G

163193310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169489005-C-T

163193493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169488830-T-C

163193519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169488807-G-A

163195774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169487605-A-G

163195932-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169487420-C-G

163195932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169487420-C-T

163195986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169487369-C-T

163196045-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169487310-C-G

163196157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169487208-G-A

163196158-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169487207-C-G

163196180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169487181-A-G

163196187-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169487174-C-G

163196311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169487048-C-T

http://identifiers.org/hco/1/GRCh38#163196487-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169486884-A-C

http://identifiers.org/hco/1/GRCh38#163196699-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169486731-A-C

163196756-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169486682-A-T

163196820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169486600-G-A

163196972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169486459-G-A

163197357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169485248-A-G

163197486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169485121-G-A

163197635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169484990-T-C

163197717-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169484925-C-G

163201169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169484574-C-T

163201831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169484085-G-A

163201944-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169483979-G-C

163202137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169483836-G-A

163202204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169483778-C-T

163202219-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169483760-G-T

163202224-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169483749-C-G

163202224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169483749-C-T

163202225-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169483748-C-G

163202257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169483716-A-G

163202257-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169483716-A-T

163202357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169483613-G-A

163202382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169483588-A-G

163202562-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169483400-G-C

163202589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169483374-A-G

163202642-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169483329-G-C

163202642-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169483329-G-T

163202658-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169483313-C-G

http://identifiers.org/hco/1/GRCh38#163202662-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169483309-C-A

163202664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169483307-A-G

163202664-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169483307-A-T

163202727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169483253-C-T

163202731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169483249-C-T

163202777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169483203-T-C

163202780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169483200-C-T

163202889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 169483093-C-T

163202926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169483057-T-C

http://identifiers.org/hco/1/GRCh38#163202985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169483000-C-A

163203035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169482951-G-A

163203035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169482951-G-T

http://identifiers.org/hco/1/GRCh38#163203057-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169482929-C-A

http://identifiers.org/hco/1/GRCh38#163203110-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169482879-A-C

163203110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169482879-A-G

163203133-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169482855-C-G

163203133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169482855-C-T

163203190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169482798-G-A

163203190-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169482798-G-T

163203353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169482660-G-A

163203378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169482635-C-T

163203547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169473362-T-C

163203559-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169473350-C-G

http://identifiers.org/hco/1/GRCh38#163203745-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169473141-A-C

163203865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169472995-T-C

163204630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169471265-G-A

163204631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169471264-G-T

163204693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169471202-G-T

163204764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169471129-A-G

http://identifiers.org/hco/1/GRCh38#163204868-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169471024-A-C

163204901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169470994-G-T

163205284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169470673-G-A

163205315-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169470572-T-A

163205330-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169470557-G-T

163205336-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169470537-T-A

163205493-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169470278-T-A

163205551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169470232-T-C

163205595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169470189-T-C

163206067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169469510-A-G

http://identifiers.org/hco/1/GRCh38#163206079-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169469480-A-C

163206111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169469448-T-C

163206564-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169468725-G-T

163206578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169468711-G-A

http://identifiers.org/hco/1/GRCh38#163206639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169468647-C-A

163206711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 169468581-G-A

163206711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 169468581-G-T

163207091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 169468195-G-A

163211801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 169465084-G-A

163211801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 169465084-G-T

http://identifiers.org/hco/1/GRCh38#163211952-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169464934-C-A

http://identifiers.org/hco/1/GRCh38#163211976-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169464909-C-A

163212036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 169464851-T-C

http://identifiers.org/hco/1/GRCh38#163212042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169464845-C-A

163212042-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 169464845-C-G

163212042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 169464845-C-T

163212146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 169464754-G-T

http://identifiers.org/hco/1/GRCh38#163212169-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169464731-C-A

163212207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 169464708-T-C

163212647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 169463331-C-T

http://identifiers.org/hco/1/GRCh38#163212911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40504
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#169462767-C-A