73749862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114067421-G-A

73749865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114067424-G-A

73750016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114067575-A-G

http://identifiers.org/hco/17/GRCh38#73750225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114067832-C-A

73750247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114067862-A-G

73750247-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114067862-A-T

73750275-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114067890-A-T

73750295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114067910-G-A

http://identifiers.org/hco/17/GRCh38#73750392-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114068014-A-C

73750398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114068020-G-A

73750398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114068020-G-T

http://identifiers.org/hco/17/GRCh38#73750484-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114068117-C-A

73750484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114068117-C-T

http://identifiers.org/hco/17/GRCh38#73750496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114068135-C-A

73750496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 114068135-C-T

73750570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114068198-T-C

73750599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114068227-A-G

73750600-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114068228-C-G

73750608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114068236-A-G

http://identifiers.org/hco/17/GRCh38#73750638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114068255-C-A

73750697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114068354-G-A

http://identifiers.org/hco/17/GRCh38#73750704-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114068361-C-A

73750704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114068361-C-T

73750832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114068492-G-A

http://identifiers.org/hco/17/GRCh38#73750882-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114068536-C-A

73750882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114068536-C-T

http://identifiers.org/hco/17/GRCh38#73750903-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114068557-A-C

73750903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114068557-A-G

73750904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114068558-G-A

73750904-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114068558-G-T

73750919-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114068569-T-G

73751011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114068661-A-G

73751021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114068671-G-A

73751021-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114068671-G-C

73751214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114068876-G-A

73751214-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114068876-G-T

73751260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 114068927-G-A

73751260-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 114068927-G-T

73751276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 114068942-G-T

73752509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114069462-T-C

73752587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114069650-G-A

73752661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114069720-C-T

73752708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114069738-G-T

73752836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114069881-G-A

73752851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114069922-G-A

73752852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114069923-G-A

73752858-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114069929-G-T

73753050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114070109-C-T

73753097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114070157-G-A

73755289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114072173-G-A

73755289-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114072173-G-T

http://identifiers.org/hco/17/GRCh38#73755407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114072300-C-A

73755503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114072396-C-T

http://identifiers.org/hco/17/GRCh38#73755620-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114072490-A-C

http://identifiers.org/hco/17/GRCh38#73756010-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114072828-C-A

73756010-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114072828-C-G

73756010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114072828-C-T

73756043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114072852-G-A

73756043-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114072852-G-T

73756044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114072853-A-G

73756044-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114072853-A-T

73756063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114072872-G-A

73756097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114072906-A-G

73756183-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114072989-G-C

73756195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114073001-C-T

73756232-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114073018-G-C

73756232-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114073018-G-T

73756237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114073023-T-C

73756311-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 114073105-G-T

73756346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114073143-T-C

http://identifiers.org/hco/17/GRCh38#73756353-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114073150-A-C

73756353-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114073150-A-T

73756370-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114073170-T-A

73756370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114073170-T-C

73756386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114073185-G-A

73756386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114073185-G-T

73756397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114073202-A-G

73756411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114073216-T-C

73756426-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114073231-C-G

73756426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114073231-C-T

73756566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114073362-C-T

http://identifiers.org/hco/17/GRCh38#73756568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114073364-C-A

73756568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114073364-C-T

73756577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114073373-T-C

73756595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114073394-A-G

http://identifiers.org/hco/17/GRCh38#73756655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114073455-C-A

73756655-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114073455-C-G

73756664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114073464-C-T

73756682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114073482-G-A

http://identifiers.org/hco/17/GRCh38#73756828-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114073637-C-A

73756828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114073637-C-T

73757087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114073918-G-A

73757100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114073931-T-C

73757127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114073958-G-A

73757258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114074092-A-G

73757433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114074285-C-T

73757466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114074318-G-A

73757495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114074347-C-T

73757886-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114074706-T-A

73757886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114074706-T-C

73757929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114074745-C-T

http://identifiers.org/hco/17/GRCh38#73757950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114074766-C-A

73757993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114074813-T-C

73757997-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114074817-T-A

73757997-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114074817-T-G

73758055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114074875-T-C

73758065-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114074885-G-T

http://identifiers.org/hco/17/GRCh38#73759142-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114075308-C-A

73759166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114075332-G-A

http://identifiers.org/hco/17/GRCh38#73759288-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114075445-C-A

73759325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114075483-A-G

73759437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114075638-T-C

73759494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114075719-G-A

73759498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114075723-G-A

73759624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114075838-T-C

http://identifiers.org/hco/17/GRCh38#73759732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114075940-C-A

73759732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114075940-C-T

73759778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114075982-G-A

73760103-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114076301-T-G

73760129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114076327-G-A

73760533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114076752-A-G

73760550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114076775-A-G

73760756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114076971-T-C

73760798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114077013-T-C

73760813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114077028-T-C

73760816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114077031-G-A

73760864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114077057-G-A

73760976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: non coding transcript exon variant
orthologous variants: 114077122-G-A

http://identifiers.org/hco/17/GRCh38#73761129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114077279-C-A

73761129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114077279-C-T

73761254-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114077400-T-G

73761476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114077572-G-A

73761565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114077669-G-A

73761846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114078043-G-A

73761856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114078053-A-G

73761909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114078089-C-T

73762219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114078381-G-A

73762317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114078476-G-A

73762406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114078564-C-T

73762488-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114078644-G-T

73762761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114078798-G-A

73765100-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114082591-C-G

73765221-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114082695-T-A

73765221-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114082695-T-G

73765491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114082982-C-T

73765495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114082986-T-C

73765569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114083073-A-G

73765574-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114083078-C-G

73765835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114083524-C-T

73765844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114083533-T-C

73765873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114083551-G-A

73765910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114083586-A-G

73765925-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114083602-C-G

73765942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114083619-G-A

73765975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114083652-G-A

73766015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114083686-T-C

73766061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114083726-G-A

73766086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114083751-G-A

73766108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114083772-T-C

73766109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114083773-C-T

73766129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114083793-G-T

73766130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114083794-T-C

73766130-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114083794-T-G

73766285-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114083938-C-G

73766285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114083938-C-T

73766471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114084118-C-T

73766478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114084124-T-C

73766770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114084388-C-T

73767346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114084901-C-T

73767368-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114084922-G-C

73767385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114084940-C-T

73767493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114085047-C-T

73767629-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114085188-C-G

73768006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114085770-C-T

73768138-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114085905-C-G

73768138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114085905-C-T

73768206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114085974-A-G

73768514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114086293-A-G

73768531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114086311-T-C

http://identifiers.org/hco/17/GRCh38#73768591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114086362-C-A

73768635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114086404-T-C

73768749-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114086517-G-C

73768837-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114086585-G-C

73769323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114087565-C-T

73769332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114087574-T-C

73769355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114087597-C-T

73769513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114087752-G-A

73770685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114089276-A-G

73770744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114089335-C-T

73770937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114089488-C-T

73770971-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114089522-C-G

73770971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114089522-C-T

http://identifiers.org/hco/17/GRCh38#73771123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114089624-C-A

http://identifiers.org/hco/17/GRCh38#73771143-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114089644-C-A

73771177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114089676-T-C

73771177-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114089676-T-G

73771413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114089870-T-C

73771859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114090463-T-C

73772234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114090765-A-G

73772254-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114090792-C-G

73772338-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114090884-T-G

73772375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114090928-C-T

73772415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114090966-T-C

73772476-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114091053-C-G

73772476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114091053-C-T

73773002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114091852-A-G

73773137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114092002-G-A

73773208-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114092081-G-C

73773208-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114092081-G-T

73773403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114092292-G-A

73773550-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114092435-T-G

73773801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114092553-G-T

73773855-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114092605-A-T

73773930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114092650-G-A

73773944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114092662-G-A

http://identifiers.org/hco/17/GRCh38#73774077-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114092796-C-A

73774612-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114093383-C-G

73774612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114093383-C-T

73774690-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114093458-T-A

73774742-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114093519-T-A

73774781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114093556-A-G

73774829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114093597-T-C

73774860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114093621-G-A

73775097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114093854-G-A

73775599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114094340-G-A

73775650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114094385-A-G

73775650-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114094385-A-T

73775672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114094400-A-G

http://identifiers.org/hco/17/GRCh38#73775718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114094424-C-A

73775736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114094437-C-T

http://identifiers.org/hco/17/GRCh38#73775998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114094701-C-A

73775998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114094701-C-T

http://identifiers.org/hco/17/GRCh38#73776435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114095721-C-A

73776435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114095721-C-T

73776506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114095791-A-G

73776508-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114095793-A-T

73776530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114095834-G-A

73776840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114096239-A-G

73776893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114096291-T-C

73776899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114096297-C-T

73776938-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114096332-G-T

73779848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114098206-T-C

73780864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114098901-T-C

73781510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114099908-C-T

73781733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114100133-A-G

73781959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114100361-G-A

73784553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114105565-C-T

http://identifiers.org/hco/17/GRCh38#73784671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114105702-C-A

73784671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114105702-C-T

73784706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114105735-T-C

73784730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114105752-T-C

http://identifiers.org/hco/17/GRCh38#73784761-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114105779-C-A

73785342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114107120-A-G

73785388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114107209-C-T

73785416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114107232-C-T

73785514-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114107323-C-G

73785514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114107323-C-T

73785559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114107368-T-C

73785595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114107434-G-A

73785640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114107479-G-A

http://identifiers.org/hco/17/GRCh38#73785684-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114107520-C-A

73785957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114107789-G-A

73786076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114107908-C-T

73786115-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114107947-T-A

73786115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114107947-T-C

73786119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114107951-C-T

73786447-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114108288-T-G

73786659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114108502-G-A

73786659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114108502-G-T

http://identifiers.org/hco/17/GRCh38#73786661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114108504-C-A

73786661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114108504-C-T

73786677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114108520-G-A

73786677-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114108520-G-T

73786825-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114108679-T-A

73787072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114108869-A-G

73787151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114108984-G-A

73787151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114108984-G-T

http://identifiers.org/hco/17/GRCh38#73787167-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114109000-C-A

73787167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114109000-C-T

http://identifiers.org/hco/17/GRCh38#73787206-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114109033-C-A

73787206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114109033-C-T

73787230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114109066-G-A

73787230-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114109066-G-C

73787230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114109066-G-T

73787274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114109107-C-T

73787649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114109492-A-G

73787649-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114109492-A-T

73787655-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114109498-A-T

73787827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114109664-T-C

73787847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114109683-G-A

73787847-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114109683-G-T

73787849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114109685-G-T

73787913-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114109750-G-C

73787913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114109750-G-T

73787995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114109835-T-C

73788035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114109875-T-C

73788192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114110065-T-C

73788263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114110150-T-C

73788315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114110202-A-G

73788333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114110220-G-A

http://identifiers.org/hco/17/GRCh38#73790403-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114114967-C-A

http://identifiers.org/hco/17/GRCh38#73790428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114114990-C-A

73790442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114114995-C-T

http://identifiers.org/hco/17/GRCh38#73790444-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114114997-C-A

73790564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 114115094-T-C

73790593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114115123-G-T

73790597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114115127-T-C

73790598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114115128-G-A

http://identifiers.org/hco/17/GRCh38#73790617-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114115147-C-A

http://identifiers.org/hco/17/GRCh38#73790619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114115149-C-A

73790664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114115194-A-G

73790669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114115199-C-T

73790738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114115224-A-G

73790788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114115274-A-G

http://identifiers.org/hco/17/GRCh38#73790810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114115296-C-A

73790810-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114115296-C-G

73790846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114115320-G-T

http://identifiers.org/hco/17/GRCh38#73790899-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114115351-A-C

73791043-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114115491-T-G

73791077-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114115551-A-T

73791093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114115567-G-A

73791107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114115581-G-A

http://identifiers.org/hco/17/GRCh38#73791165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114115634-C-A

73791423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114115862-G-A

http://identifiers.org/hco/17/GRCh38#73791455-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114115898-C-A

73791455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114115898-C-T

http://identifiers.org/hco/17/GRCh38#73791635-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114116083-C-A

73791642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114116090-T-C

73791644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114116092-G-A

73791644-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114116092-G-C

73791649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114116097-G-A

73791698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114116145-T-C

http://identifiers.org/hco/17/GRCh38#73791808-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114116255-C-A

73791808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114116255-C-T

73791846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114116290-A-G

http://identifiers.org/hco/17/GRCh38#73791890-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114116331-C-A

73791894-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114116342-A-T

http://identifiers.org/hco/17/GRCh38#73791895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114116343-C-A

http://identifiers.org/hco/17/GRCh38#73791899-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114116347-C-A

73791899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114116347-C-T

http://identifiers.org/hco/17/GRCh38#73791900-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114116348-C-A

73791901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114116349-T-C

73792105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114116477-T-C

73792170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114116515-A-G

73792440-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114116742-G-T

73792541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114116824-A-G

http://identifiers.org/hco/17/GRCh38#73792561-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114116845-A-C

73792636-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114116927-G-C

73792697-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114117383-G-C

73792715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114117401-T-C

73793096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114117765-C-T

73793163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114117831-G-T

73793180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114117847-G-A

73793277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114117940-G-A

73793277-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114117940-G-C

http://identifiers.org/hco/17/GRCh38#73793287-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114117950-C-A

73793287-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114117950-C-G

73793287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114117950-C-T

http://identifiers.org/hco/17/GRCh38#73797214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114122429-C-A

73797364-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114122559-T-A

73797365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114122560-C-T

73797420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114122621-C-T

73797428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114122629-G-A

73797428-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114122629-G-T

73797437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114122638-G-A

73797535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114122651-T-C

73797794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114122885-A-G

http://identifiers.org/hco/17/GRCh38#73797810-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114122901-A-C

73797904-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114122999-T-A

73797910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114123005-G-A

73797984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114123068-G-A

73798761-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114123666-T-A

73798761-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114123666-T-G

73799108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114123860-G-A

73799108-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114123860-G-T

73799125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114123870-G-A

73799125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114123870-G-T

73799126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114123871-G-A

73799126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114123871-G-T

73799130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114123875-A-G

73799132-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114123877-G-T

73799205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114123956-A-G

73799238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114123989-G-T

http://identifiers.org/hco/17/GRCh38#73799246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114123997-C-A

73799246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114123997-C-T

73799265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114124016-C-T

73799275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114124030-G-A

73799275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114124030-G-T

73799306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114124069-G-T

73799921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114124353-G-A

http://identifiers.org/hco/17/GRCh38#73799927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114124359-C-A

73799927-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114124359-C-G

73799932-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114124364-T-A

73799932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114124364-T-C

73799932-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114124364-T-G

73800024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114124411-G-A

73800235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114124612-A-G

73800328-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114124700-G-T

73800332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114124704-T-C

73800685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114125018-A-G

73800685-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114125018-A-T

73801397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114125686-G-A

73801418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114125706-G-A

73801780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114127023-C-T

73801796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114127043-A-G

73802308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114128137-T-C

73802338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114128160-A-G

73802437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114128255-G-A

73802880-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114128599-A-T

73802958-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114128676-T-G

73803285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114129078-G-A

73803297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114129122-T-C

73803343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114129202-C-T

73803554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114129672-C-T

73803617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114129727-T-C

73803769-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114129864-T-G

73803785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114129880-C-T

http://identifiers.org/hco/17/GRCh38#73803942-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114130056-C-A

73804430-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114130553-T-A

73804430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114130553-T-C

http://identifiers.org/hco/17/GRCh38#73804761-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114131251-A-C

73804804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114131286-G-T

73804863-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114131342-G-C

http://identifiers.org/hco/17/GRCh38#73805054-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114131506-C-A

73805205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114131647-G-A

73806248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114132081-A-G

http://identifiers.org/hco/17/GRCh38#73806271-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114132115-A-C

73811973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114133929-T-C

73812177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114134072-G-A

73812581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114134472-T-C

http://identifiers.org/hco/17/GRCh38#73812657-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114134543-A-C

http://identifiers.org/hco/17/GRCh38#73813089-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114134965-C-A

73813110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114134986-G-A

73813141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114134992-A-G

73814312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114137291-A-G

73814610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114137591-T-C

http://identifiers.org/hco/17/GRCh38#73814749-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114137731-C-A

73814749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114137731-C-T

73817771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114140573-G-A

73817771-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114140573-G-T

73817812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114140610-G-A

73817974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114140746-G-A

73818170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114140997-A-G

73818390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114141347-T-C

73818446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114141395-C-T

73818525-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114141473-T-G

http://identifiers.org/hco/17/GRCh38#73818556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114141500-C-A

73818589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114141534-G-A

73818619-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114141564-T-G

73818621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114141566-A-G

73818630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114141575-A-G

73818648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114141594-A-G

73818655-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114141601-T-G

http://identifiers.org/hco/17/GRCh38#73818700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114141653-C-A

73818708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114141662-G-A

http://identifiers.org/hco/17/GRCh38#73818763-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114141701-A-C

73820916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114142401-T-C

73821037-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114142502-T-G

73821074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114142538-A-G

73821578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114142983-G-T

73822174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114143460-T-C

http://identifiers.org/hco/17/GRCh38#73822220-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114143492-A-C

73822562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114143751-G-A

73822573-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114143771-A-T

73822583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114143790-C-T

73822607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114143814-C-T

73822633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114143837-G-T

73822660-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114143856-A-T

73823171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114144056-G-T

73824439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114144864-G-A

73824439-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114144864-G-C

73824567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114145008-G-A

73824567-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114145008-G-C