46921731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 110540656-G-A

46921731-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 110540656-G-C

46921731-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 110540656-G-T

46921940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 110540513-A-G

46921973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 110540487-G-A

46921973-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 110540487-G-T

46921975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 110540485-T-C

46922012-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 110540449-T-A

46922012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 110540449-T-C

46922091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110540365-G-A

46922368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110540097-T-C

46922369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110540096-G-A

46922370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110540095-G-A

46922466-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110540026-T-A

46922466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110540026-T-C

46922466-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110540026-T-G

46922471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110540023-T-C

http://identifiers.org/hco/3/GRCh38#46922477-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110540017-A-C

46922477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110540017-A-G

46922477-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110540017-A-T

http://identifiers.org/hco/3/GRCh38#46922544-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110539957-A-C

46922544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110539957-A-G

46922607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110539900-C-T

46922610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110539897-G-A

46922610-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110539897-G-T

http://identifiers.org/hco/3/GRCh38#46922616-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110539891-A-C

46922616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110539891-A-G

46922643-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110539864-T-A

46922643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110539864-T-C

http://identifiers.org/hco/3/GRCh38#46922674-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110539832-C-A

46922674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110539832-C-T

http://identifiers.org/hco/3/GRCh38#46922695-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110539811-C-A

46922695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110539811-C-T

46922714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110539795-T-C

http://identifiers.org/hco/3/GRCh38#46922715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110539794-C-A

46922730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110539779-G-A

46922730-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110539779-G-T

46922738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110539771-G-A

46922738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110539771-G-T

46922794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110539718-T-C

http://identifiers.org/hco/3/GRCh38#46922985-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110539547-A-C

http://identifiers.org/hco/3/GRCh38#46923023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110539501-C-A

46923023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110539501-C-T

http://identifiers.org/hco/3/GRCh38#46923024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110539500-C-A

46923043-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110539482-T-G

46923093-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110539436-G-T

http://identifiers.org/hco/3/GRCh38#46923144-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110539388-C-A

46923144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110539388-C-T

46923212-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110539327-T-A

46923212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110539327-T-C

46923215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110539324-G-A

46923215-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110539324-G-T

46923219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110539320-G-A

46923219-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110539320-G-T

http://identifiers.org/hco/3/GRCh38#46923225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110539314-C-A

46923225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110539314-C-T

46923282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110539258-A-G

46923378-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110539178-G-C

46923445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110539110-G-A

46923452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110539103-A-G

46923512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110539069-G-T

46923690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110538938-A-G

46923695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110538933-G-A

46923695-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110538933-G-T

http://identifiers.org/hco/3/GRCh38#46923696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110538932-C-A

46923698-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110538930-T-A

46923698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110538930-T-C

46923698-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110538930-T-G

46923710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110538923-G-A

46923710-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110538923-G-C

46923710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110538923-G-T

46923726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110538907-G-A

46923726-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110538907-G-T

http://identifiers.org/hco/3/GRCh38#46923729-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110538905-A-C

46923729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110538905-A-G

46923849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110538841-G-A

46923849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110538841-G-T

46923863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110538827-G-A

46923863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110538827-G-T

46923879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110538811-G-A

46923879-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110538811-G-T

46923921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110538772-A-G

46923921-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110538772-A-T

46923923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110538770-G-A

46923923-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110538770-G-C

http://identifiers.org/hco/3/GRCh38#46923972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110538736-C-A

http://identifiers.org/hco/3/GRCh38#46924041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110538687-C-A

46924041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110538687-C-T

46924081-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110538643-A-T

http://identifiers.org/hco/3/GRCh38#46924117-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110538623-A-C

46924117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110538623-A-G

http://identifiers.org/hco/3/GRCh38#46924121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110538619-C-A

46924152-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110538599-G-T

46924195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110538573-A-G

46924195-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110538573-A-T

46924242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110538551-A-G

46924265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110538542-A-G

http://identifiers.org/hco/3/GRCh38#46924280-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110538527-C-A

46924280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110538527-C-T

46924310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110538497-A-G

46924762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110538020-G-A

http://identifiers.org/hco/3/GRCh38#46924811-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110537975-A-C

46924811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110537975-A-G

46925162-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110537768-T-A

46925380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110537634-A-G

46925380-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110537634-A-T

46925422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110537623-A-G

46925540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 110537507-A-G

46925637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110537427-T-C

46925875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110537259-A-G

http://identifiers.org/hco/3/GRCh38#46925884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110537250-C-A

http://identifiers.org/hco/3/GRCh38#46925949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110537203-C-A

46926118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110537024-T-C

46926142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110536987-G-A

46926435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110536700-G-A

46926550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110536632-G-A

46926551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110536631-C-T

46926640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110536555-G-A

46926770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110536467-C-T

46926930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110536348-C-T

46927207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110536168-C-T

46927240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110536143-G-A

46929159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110532938-T-C

46930316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110531057-C-T

46930371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110531025-G-A

46930408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110531012-A-G

46930409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110531011-G-A

http://identifiers.org/hco/3/GRCh38#46930561-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110530891-A-C

http://identifiers.org/hco/3/GRCh38#46930836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110530665-C-A

46931209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110530335-G-A

46931309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110530180-G-A

46931423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110530094-A-G

46931431-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110530086-T-A

http://identifiers.org/hco/3/GRCh38#46931440-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110530077-A-C

46931495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110530027-G-A

46931590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110529937-T-C

46931672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110529867-G-A

46932127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110529370-C-T

46932163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110529335-G-A

46932183-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110529316-T-A

46932183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110529316-T-C

46932233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110529280-C-T

46932388-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110529071-G-C

46933666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110528708-G-A

46934602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110526396-G-A

46934626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110526371-A-G

46934805-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110526176-A-T

46935578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110525635-C-T

46935772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110525520-G-A

46935797-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110525499-C-G

46935879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110525427-T-C

http://identifiers.org/hco/3/GRCh38#46936131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110525087-C-A

46936179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110525041-G-A

46936806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110524454-G-A

46937084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110524200-C-T

46937397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110523939-C-T

46937537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110523821-G-A

46937817-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110523604-G-C

46938278-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110523354-A-T

46938351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110523280-G-A

46939339-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110522745-C-G

46939506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110522587-G-A

46940824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110521640-G-A

46940824-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110521640-G-T

46940874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110521596-A-G

46940874-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110521596-A-T

http://identifiers.org/hco/3/GRCh38#46940909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110521579-C-A

46940909-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110521579-C-G

46940909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110521579-C-T

46940992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110521455-C-T

46941098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110521350-T-C

46941098-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110521350-T-G

46941109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110521339-T-C

http://identifiers.org/hco/3/GRCh38#46941178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110521296-C-A

46941178-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110521296-C-G

46941178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110521296-C-T

46941359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110521186-G-A

http://identifiers.org/hco/3/GRCh38#46941608-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110521060-A-C

46941651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110521033-A-G

46941651-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110521033-A-T

46941664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110521023-T-C

46942925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110519741-C-T

46942949-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110519717-A-T

46943123-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110519359-G-C

46943149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110519334-G-A

46943523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110518881-G-A

46943566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110518846-A-G

46943718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110518680-C-T

46943864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110518546-A-G

46944102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110518333-C-T

46945937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110516368-C-T

46945993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110516310-A-G

46946193-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110516145-T-G

http://identifiers.org/hco/3/GRCh38#46946432-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110515945-A-C

46946573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110515830-C-T

46946858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110515616-A-G

46946862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110515612-C-T

46946916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110515565-A-G

46947023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110515467-G-A

http://identifiers.org/hco/3/GRCh38#46947042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110515448-C-A

46947147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110515185-A-G

46947245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110515031-A-G

46947373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110514900-G-A

46947425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110514847-G-A

46947425-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110514847-G-C

http://identifiers.org/hco/3/GRCh38#46947503-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110514769-A-C

46947738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110514537-A-G

http://identifiers.org/hco/3/GRCh38#46947758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110514517-C-A

46947789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110514503-T-C

46947938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110514360-G-A

46948369-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110513757-C-G

46948700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110513453-C-T

46948791-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110513363-C-G

46949546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110512546-G-A

46949595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110512496-T-C

46949885-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110512205-G-C

46949900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110512190-G-A

46949902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110512188-C-T

46949904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110512186-G-A

46949946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110512146-G-A

46949960-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110512130-T-A

46950005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110512096-G-A

http://identifiers.org/hco/3/GRCh38#46950021-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110512080-A-C

46950021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110512080-A-G

http://identifiers.org/hco/3/GRCh38#46950049-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110512052-A-C

46953029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110511347-A-G

46953341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110511094-A-G

46953606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110510814-T-C

46953798-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110510512-G-C

46954458-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110509174-T-A

46955367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110507000-G-A

46955630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110506769-C-T

46955928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110506337-C-T

46956228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110506025-G-A

46956228-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110506025-G-C

46956458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110505836-G-A

46958724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110504609-G-A

46958782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110504568-A-G

46959377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110503821-C-T

46959489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110503710-G-A

46959882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110502950-C-T

46960359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110502556-G-A

46960359-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110502556-G-C

46960369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110502546-A-G

46960454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110502510-G-A

46960454-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110502510-G-C

46960579-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110502389-T-A

46960767-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110502203-T-G

46960957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110502102-G-A

46966732-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110499491-C-G

46966838-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110499384-G-C

46967601-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110499024-A-T

46967804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110498870-G-A

http://identifiers.org/hco/3/GRCh38#46967827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110498849-C-A

46967942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110498739-A-G

46967969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110498713-G-A

http://identifiers.org/hco/3/GRCh38#46968281-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110498161-C-A

46968672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110497783-C-T

46968928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110497373-T-C

46969083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110497220-T-C

46969226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110497100-G-A

46969280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110497053-G-A

46970486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110496687-G-A

46970608-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110496577-G-C

46970669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110496498-G-A

46970771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110496393-G-A

46970771-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110496393-G-C

46971098-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110495928-C-G

46971143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110495908-T-C

46971184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110495871-G-A

46971288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110495758-A-G

46971792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110495301-T-C

46971992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110495118-G-A

46976176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110486126-G-A

46976176-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110486126-G-C

46976176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110486126-G-T

46976258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110486061-G-A

46976258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110486061-G-T

http://identifiers.org/hco/3/GRCh38#46976276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110486051-C-A

http://identifiers.org/hco/3/GRCh38#46976291-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110486036-A-C

46976291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110486036-A-G

46976308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110486004-T-C

46976476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110485863-G-A

46976476-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110485863-G-C

46976476-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110485863-G-T

46976602-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110485760-C-G

46976602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110485760-C-T

http://identifiers.org/hco/3/GRCh38#46976607-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110485755-C-A

46976607-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110485755-C-G

46976607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110485755-C-T

46976721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 110485640-A-G

46976763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 110485600-G-A

http://identifiers.org/hco/3/GRCh38#46976789-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110485576-A-C

http://identifiers.org/hco/3/GRCh38#46976804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110485561-C-A

46976804-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110485561-C-G

46976804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110485561-C-T

46976872-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110485494-T-G

http://identifiers.org/hco/3/GRCh38#46976987-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110485421-A-C

46976987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110485421-A-G

46976987-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110485421-A-T

http://identifiers.org/hco/3/GRCh38#46977004-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110485404-C-A

46977004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110485404-C-T

46977038-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 110485373-G-C

46977425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110485118-A-G

46977523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110485064-C-T

46977607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110484969-G-A

46977747-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110484846-T-A

46978192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110484239-C-T

46978312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110484115-G-A

46978429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110484085-G-A

46978697-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110483858-G-C

46979213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110483670-C-T

46979354-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110483527-T-A

46979354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110483527-T-C

46979354-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110483527-T-G

http://identifiers.org/hco/3/GRCh38#46979396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110483485-C-A

46979442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110483441-T-C

46979442-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110483441-T-G

46979453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110483430-G-A

46979478-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110483425-A-T

46979500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110483403-C-T

46979664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110483216-G-A

46979664-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110483216-G-C

46979664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110483216-G-T

46979685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110483192-C-T

http://identifiers.org/hco/3/GRCh38#46979979-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#110482908-C-A

46979979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110482908-C-T

46980003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110482885-G-A

46981526-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110481941-G-C

46982005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28332
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110481615-G-T