132685130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66380590-A-G

132685130-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66380590-A-T

132685155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66380637-A-G

132685155-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66380637-A-T

132685236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66380751-G-A

http://identifiers.org/hco/8/GRCh38#132685360-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66380871-C-A

132685497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66381019-C-T

132685837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66381942-A-G

132686045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66382122-A-G

132686380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66382417-G-A

132686657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66382604-G-A

132687052-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66383009-G-T

132687102-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66383058-A-T

132687324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66383238-G-A

132687324-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66383238-G-C

132687324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66383238-G-T

132687330-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66383244-G-C

132687330-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66383244-G-T

132687416-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66383325-T-G

http://identifiers.org/hco/8/GRCh38#132687551-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66383459-C-A

http://identifiers.org/hco/8/GRCh38#132687803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66384070-C-A

132687803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66384070-C-T

132698349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66384840-T-C

132698387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66384880-G-A

132701001-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66385333-C-G

132701156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66385483-G-A

132701190-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66385513-G-C

132701204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66385527-T-C

132701243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66385565-T-C

132701504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66385718-G-A

132701696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66385797-T-C

132701846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66385942-C-T

132703006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66386308-G-A

132703006-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66386308-G-C

132703056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66386349-C-T

132703242-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66386541-T-A

132703242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66386541-T-C

132703253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66386553-T-C

132703592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 66386886-T-C

132703600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 66386894-C-T

132703690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66386976-G-A

132703690-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66386976-G-C

132703795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 66387083-C-T

132703932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66387193-A-G

132704156-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66387395-C-G

132704156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66387395-C-T

http://identifiers.org/hco/8/GRCh38#132704247-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#66387477-A-C

132704247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 66387477-A-G

132704308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 66387526-A-G

132704440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 66387654-T-C

132704825-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66388050-G-C

132704974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66388234-T-C

132705062-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66388325-T-G

132705082-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66388345-A-T

132705257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66388506-C-T

132705296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66388544-A-G

132705546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66388676-A-G

132705664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66388783-G-A

132705664-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66388783-G-C

132705674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66388793-A-G

132706042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 66389565-C-T

132706088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 66389610-C-T

132706191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66389699-G-T

132706495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66389976-A-G

132706802-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66390190-C-G

132706802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66390190-C-T

132706963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66390342-G-A

132706963-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66390342-G-C

http://identifiers.org/hco/8/GRCh38#132706996-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66390374-A-C

132707152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66390496-A-G

132707781-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66393010-A-T

132710235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66398691-G-A

132710235-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66398691-G-T

132710349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66398810-T-C

132710349-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66398810-T-G

132710365-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66398829-T-G

132710533-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66399346-C-G

http://identifiers.org/hco/8/GRCh38#132710569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66399382-C-A

http://identifiers.org/hco/8/GRCh38#132710609-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66399425-C-A

132710648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66399463-G-A

132710648-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66399463-G-T

http://identifiers.org/hco/8/GRCh38#132710656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66399471-C-A

132710656-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66399471-C-G

132710656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66399471-C-T

132710672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66399486-T-C

132710672-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66399486-T-G

http://identifiers.org/hco/8/GRCh38#132710714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66399527-C-A

132710718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66399532-G-A

132710718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66399532-G-T

132710757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66399572-G-A

132710757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66399572-G-T

132710786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66399601-T-C

132710817-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66399629-T-A

132710852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66399663-C-T

http://identifiers.org/hco/8/GRCh38#132710891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66399704-C-A

132710891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 66399704-C-T

132710919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 66399730-C-T

132710929-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 66399740-G-T

132710932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 66399743-G-A

132710932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 66399743-G-T

132710933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 66399744-G-A

132710933-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 66399744-G-C

132710933-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 66399744-G-T

132710945-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 66399756-C-G

132710945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 66399756-C-T

http://identifiers.org/hco/8/GRCh38#132710956-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: http://identifiers.org/mco/15/GRCm39#66399767-C-A

132710956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 66399767-C-T

132710964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 66399775-T-C

132710991-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66399792-G-C

132711026-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66399819-T-A

132711026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66399819-T-C

132711038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66399832-G-A

132711038-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66399832-G-T

132711113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66399863-A-G

132711242-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66400005-G-T

132711251-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66400014-T-A

132711274-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66400037-C-G

132711578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66400834-A-G

132711598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66400853-C-T

132711632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66400881-C-T

132711977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66401327-T-C

132712158-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66401492-C-G

132712158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66401492-C-T

132712301-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66401649-T-A

132712301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66401649-T-C

132712347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 66401683-G-A

http://identifiers.org/hco/8/GRCh38#132712426-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66401764-C-A

132713158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66403600-C-T

132713198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66403640-T-C

132713276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66403717-G-A

132713276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66403717-G-T

132713278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66403719-G-A

132713328-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66403770-A-T

132713449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66403928-T-C

132713486-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66403965-G-C

132713486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66403965-G-T

132713702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66404125-A-G

132713764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66404185-G-A

132713764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66404185-G-T

132713830-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66404251-G-T

132713885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66404308-A-G

132713917-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66404363-T-A

132713917-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66404363-T-G

http://identifiers.org/hco/8/GRCh38#132713922-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66404368-C-A

132713922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66404368-C-T

132714049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 66404492-A-G

132714103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66404550-T-C

132714126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66404573-T-C

132714133-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66404580-A-T

132714166-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 66404612-T-A

132714233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66404679-C-T

132714309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66404757-G-A

132714309-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66404757-G-T

http://identifiers.org/hco/8/GRCh38#132714323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66404771-C-A

132714323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66404771-C-T

132714367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66404816-A-G

132714480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66405161-T-C

http://identifiers.org/hco/8/GRCh38#132714579-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66405277-A-C

132714655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66405351-G-A

132714777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66405476-G-A

132714778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66405477-C-T

132714834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66405532-T-C

132714886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66405639-T-C

132714932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66405725-T-C

132719924-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66408223-A-T

132720172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66408454-T-C

132720212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66408499-C-T

132720280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66408566-T-C

132720318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66408605-C-T

132720372-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66408661-G-T

132720579-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66408848-C-G

132720651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66408919-G-A

http://identifiers.org/hco/8/GRCh38#132720700-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66408966-A-C

http://identifiers.org/hco/8/GRCh38#132720972-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66409501-A-C

132721018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66409552-G-A

132721035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66409571-G-T

http://identifiers.org/hco/8/GRCh38#132721856-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66410457-C-A

132721877-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66410482-G-C

132721880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66410485-A-G

http://identifiers.org/hco/8/GRCh38#132721916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66410520-C-A

132721916-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66410520-C-G

132721916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66410520-C-T

132721924-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66410528-A-T

132721931-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66410535-A-T

132721959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66410563-G-A

132721959-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66410563-G-C

132721959-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66410563-G-T

132721966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66410570-G-A

132721966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66410570-G-T

132722025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66410631-T-C

132722026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66410632-A-G

132722031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66410637-G-A

132722031-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66410637-G-C

132722031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66410637-G-T

http://identifiers.org/hco/8/GRCh38#132722191-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66410790-A-C

132722191-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66410790-A-T

132722224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66410803-G-A

132722224-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66410803-G-T

132722238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66410817-G-A

132722238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66410817-G-T

132722248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66410827-G-A

132722248-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66410827-G-T

132722251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66410830-A-G

132722312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66411083-T-C

http://identifiers.org/hco/8/GRCh38#132722426-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66411202-A-C

132722502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66411299-A-G

132722603-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66411400-G-C

132722617-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66411414-T-G

132722859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66411663-A-G

132722943-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66411746-A-T

132723152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66411956-A-G

http://identifiers.org/hco/8/GRCh38#132726095-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66412239-A-C

http://identifiers.org/hco/8/GRCh38#132726161-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66412300-A-C

132726184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66412323-G-A

132726265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66412417-A-G

132726318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66412463-G-A

132726318-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66412463-G-C

132726378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66412518-G-A

132726607-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66412772-T-G

132726648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66412812-T-C

132726649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66412813-G-A

132726724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66412894-A-G

132726823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66412968-G-A

http://identifiers.org/hco/8/GRCh38#132726845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66412996-C-A

132726845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66412996-C-T

132726851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66413002-C-T

132727610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66413247-T-C

http://identifiers.org/hco/8/GRCh38#132727670-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66413298-A-C

132727670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66413298-A-G

132727670-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66413298-A-T

132727711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66413339-T-C

132727742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66413370-G-T

132727915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, missense_variant
orthologous variants: 66413539-T-C

132727918-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, missense_variant
orthologous variants: 66413542-T-A

132727918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, missense_variant
orthologous variants: 66413542-T-C

132727926-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, missense_variant
orthologous variants: 66413550-T-A

132727989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 66413610-G-A

132728866-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66414975-C-G

132728987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66415093-G-T

132729293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66415394-G-A

132729293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66415394-G-T

132729306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66415402-C-T

132729349-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66415439-C-G

132729407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66415496-T-C

http://identifiers.org/hco/8/GRCh38#132729598-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66415691-A-C

132729621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66415714-G-A

132729670-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66415761-G-T

132729722-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66415802-G-C

132729738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66415820-G-A

132729739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66415821-G-T

132731434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66416798-G-A

132731635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66416955-C-T

132731648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66416968-G-A

132731755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66417074-T-C

http://identifiers.org/hco/8/GRCh38#132731815-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66417131-A-C

132731815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66417131-A-G

132731848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66417169-G-A

132731848-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66417169-G-T

132731916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66417232-G-A

132731966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66417285-T-C

132732250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66417474-G-A

http://identifiers.org/hco/8/GRCh38#132732334-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66417557-A-C

132732347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66417572-A-G

132732551-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66417765-G-C

132732583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66417797-G-A

132732663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66417868-T-C

132732708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66417915-C-T

http://identifiers.org/hco/8/GRCh38#132733544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66418034-C-A

132733643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66418132-C-T

132733702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66418174-C-T

132733713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66418185-C-T

http://identifiers.org/hco/8/GRCh38#132733716-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66418188-C-A

132733781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66418247-A-G

132733781-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66418247-A-T

132733900-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66418364-T-A

132734057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66418479-G-A

132734299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66418706-A-G

132734351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66418758-G-T

132734369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66418777-C-T

132734472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66418878-G-A

132734493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66418899-A-G

132734513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66418923-C-T

132734594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66419013-A-G

132734816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66419228-G-A

132734816-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66419228-G-C

132734816-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66419228-G-T

132735170-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66419331-G-T

132735299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66419479-T-C

http://identifiers.org/hco/8/GRCh38#132735459-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66419640-C-A

132735459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66419640-C-T

http://identifiers.org/hco/8/GRCh38#132735671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66419853-C-A

132738049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66421336-A-G

132738083-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66421367-C-G

132738191-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66421471-G-C

132738238-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66421515-T-G

http://identifiers.org/hco/8/GRCh38#132738304-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66421536-C-A

132738395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66421625-A-G

132738469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66421690-C-T

132738606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66421838-T-C

132738665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66421896-A-G

132738678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66421910-A-G

http://identifiers.org/hco/8/GRCh38#132738907-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66422135-C-A

132738938-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66422162-G-T

132738974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66422198-T-C

http://identifiers.org/hco/8/GRCh38#132738982-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66422206-C-A

132740733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66422622-C-T

132740768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66422657-C-T

http://identifiers.org/hco/8/GRCh38#132746421-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66423255-A-C

132746421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66423255-A-G

132746421-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66423255-A-T

http://identifiers.org/hco/8/GRCh38#132746425-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66423259-A-C

132746425-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66423259-A-T

132746426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66423260-T-C

132746426-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66423260-T-G

132746470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66423304-T-C

132746475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66423308-A-G

http://identifiers.org/hco/8/GRCh38#132746509-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66423341-A-C

132746509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66423341-A-G

132746509-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66423341-A-T

132746534-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66423368-T-A

132746534-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66423368-T-G

132746690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66423521-C-T

132746755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66423589-A-G

132746801-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66423629-T-A

132746801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66423629-T-C

132746805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66423633-G-A

132746805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66423633-G-T

132746811-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66423639-T-A

132746811-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66423639-T-G

132746820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66423648-G-T

http://identifiers.org/hco/8/GRCh38#132746826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66423656-C-A

132746826-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66423656-C-G

132746826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66423656-C-T

http://identifiers.org/hco/8/GRCh38#132746829-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66423659-C-A

132746829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66423659-C-T

http://identifiers.org/hco/8/GRCh38#132746854-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66423684-C-A

132746875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66423705-G-T

132746935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 66423771-A-G

132746997-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: missense variant
orthologous variants: 66423833-T-A

132746997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: synonymous variant
orthologous variants: 66423833-T-C

132747071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 66423907-G-A

132747071-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 66423907-G-C

132747172-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66424022-T-A

132747172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66424022-T-C

132747185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66424035-G-A

132747185-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66424035-G-T

132747217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66424063-A-G

132747453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66425389-C-T

132747463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66425399-T-C

132747493-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66425429-C-G

132747495-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66425431-G-T

132747518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66425453-A-G

132747626-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66425560-T-A

132747674-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66425605-G-T

132747774-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66425687-G-C

132747801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66425716-G-T

132747852-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66425767-G-C

132747912-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66425825-T-A

132751195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66426444-C-T

132751308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66426551-T-C

132751424-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66426658-G-C

132751448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66426680-C-T

132751485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66426718-A-G

http://identifiers.org/hco/8/GRCh38#132751656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66426771-C-A

132751709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66426813-A-G

132751710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66426814-G-T

132751721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66426825-A-G

132751728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66426832-A-G

132751758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66426854-T-C

132751805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: missense_variant, non_coding_transcript_exon_variant, start_lost
orthologous variants: 66426900-C-T

132751939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 66427034-G-A

132751939-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 66427034-G-T

132751948-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 66427043-T-A

132751948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 66427043-T-C

132751955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 66427050-G-A

132751955-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 66427050-G-T

132751968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 66427063-T-C

132751968-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 66427063-T-G

132752013-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66427108-T-A

132752021-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66427116-T-G

http://identifiers.org/hco/8/GRCh38#132752041-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66427136-A-C

132752111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66427211-T-C

132752153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66427253-G-A

132752177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66427260-C-T

132752178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66427261-G-A

132752287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66427370-T-C

132752287-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66427370-T-G

http://identifiers.org/hco/8/GRCh38#132752367-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66427457-C-A

132752367-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66427457-C-G

132755111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66427719-G-A

132755209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66427811-C-T

132755343-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66427968-T-A

132755368-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66427993-C-G

132755368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66427993-C-T

132755406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66428032-T-C

132755556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66428173-G-A

132755933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66428536-G-A

132756089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66428687-A-G

132757223-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66429584-C-G

132757223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66429584-C-T

http://identifiers.org/hco/8/GRCh38#132757290-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66429650-A-C

132757381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66429707-G-A

132757381-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66429707-G-C

132757381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66429707-G-T

132757408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66429730-G-A

132757408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66429730-G-T

132757410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66429732-G-A

132757430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66429752-T-C

132757519-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66429872-C-G

132757519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66429872-C-T

132757929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66429974-G-A

http://identifiers.org/hco/8/GRCh38#132758017-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66430067-C-A

132758017-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66430067-C-G

132758177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66430409-G-A

132758177-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66430409-G-T

132758216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66430499-G-T

132758325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66430610-A-G

132758374-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66430659-G-C

132758374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66430659-G-T

132758375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66430660-G-A

132758375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66430660-G-T

132758392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66430690-G-A

132758392-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66430690-G-T

http://identifiers.org/hco/8/GRCh38#132758558-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66430849-C-A

132758558-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66430849-C-G

132758715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66431008-A-G

132758872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 66431161-C-T

132758873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 66431162-G-A

132758873-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 66431162-G-C

132758927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66431223-G-A

132758927-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66431223-G-T

132759040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66431337-T-C

http://identifiers.org/hco/8/GRCh38#132759054-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66431350-C-A

132759054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66431350-C-T

http://identifiers.org/hco/8/GRCh38#132759223-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66431501-A-C

http://identifiers.org/hco/8/GRCh38#132759448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66431692-C-A

132759661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66431954-C-T

132759696-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66431989-C-G

132759696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66431989-C-T

132759815-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66432103-A-T

http://identifiers.org/hco/8/GRCh38#132759880-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66432167-C-A

132760161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66432452-A-G

132760316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66432602-A-G

132760361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66432647-C-T

132760534-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66432814-G-T

http://identifiers.org/hco/8/GRCh38#132760542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#66432822-C-A

132760542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66432822-C-T

132760644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 66432920-G-A

132760644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 66432920-G-T

132760702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 66432978-G-A

132760702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 66432978-G-T

132760728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66432991-G-T

132760770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66433033-C-T

132760885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66433141-G-A

132760885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron variant
orthologous variants: 66433141-G-T

132760975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, undefined
orthologous variants: 66433235-G-A

132760975-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26572
most severe consequence: intron_variant, undefined
orthologous variants: 66433235-G-C