130506543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30748720-C-T

130506822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30749001-A-G

130507022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30749189-A-G

130507180-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30749344-T-G

130507323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30749454-C-T

130507965-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30750047-A-T

http://identifiers.org/hco/7/GRCh38#130508032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#30750117-C-A

130508032-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30750117-C-G

130508505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30750494-G-A

130508505-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30750494-G-C

http://identifiers.org/hco/7/GRCh38#130508700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#30750674-C-A

130508700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30750674-C-T

130508713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30750684-T-C

130508778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30750765-G-T

130508861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30750846-C-T

130508901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30750878-G-A

http://identifiers.org/hco/7/GRCh38#130508964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#30750941-C-A

130508964-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30750941-C-G

130508964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30750941-C-T

130508983-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30750957-T-A

130508983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30750957-T-C

http://identifiers.org/hco/7/GRCh38#130509022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#30750979-C-A

130509022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30750979-C-T

http://identifiers.org/hco/7/GRCh38#130509085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#30751043-C-A

130509462-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30751392-T-A

130509462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30751392-T-C

http://identifiers.org/hco/7/GRCh38#130509567-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#30751486-C-A

130509567-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30751486-C-G

130509826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30751673-G-A

130509829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30751676-G-T

130510997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30752127-T-C

130511250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30752320-T-C

130511384-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30752396-C-G

130511491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30752467-G-A

130511507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30752483-T-C

http://identifiers.org/hco/7/GRCh38#130523154-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#30757223-C-A

130523154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30757223-C-T

http://identifiers.org/hco/7/GRCh38#130523161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#30757230-C-A

130523161-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30757230-C-G

130523209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30757259-C-T

130523252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30757306-G-A

130523253-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30757307-A-T

130523258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30757312-G-A

130523589-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30757574-G-C

130523696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30757710-G-A

130524271-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30758148-G-T

130524320-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30758195-G-T

130524454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30758313-G-A

130527310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30765312-G-A

130527310-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30765312-G-T

130527446-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30765445-T-G

130527458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30765458-G-A

130527478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30765481-G-A

130527814-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30765747-G-C

http://identifiers.org/hco/7/GRCh38#130527922-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-C

130528454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30762039-G-A

130529118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30766480-G-A

130529252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30766613-G-A

130529252-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30766613-G-T

130529402-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30766775-T-A

130529412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30766785-T-C

130529493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30766862-G-A

130529554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30766925-C-T

130531531-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30768803-C-G

130531708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30768970-A-G

130531810-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30769053-C-G

130531810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30769053-C-T

130531825-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30769068-T-G

130531838-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30769081-T-G

130531846-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30769089-T-A

130531846-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30769089-T-G

130532129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30769310-T-C

130532130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30769311-G-A

130532466-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30769648-G-C

130532471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30769664-G-A

130532672-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30769825-T-G

http://identifiers.org/hco/7/GRCh38#130533059-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#30770153-A-C

130533083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30770180-A-G

130536195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30775108-G-A

130536288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30775187-C-T

130536342-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30775241-C-G

130536342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30775241-C-T

130536396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30775298-G-A

130536417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30775316-A-G

130536424-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30775322-C-G

130536666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30775504-G-A

130536749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30775588-C-T

130536830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30775694-G-A

130536990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30775833-A-G

130536990-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30775833-A-T

130536993-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30775836-T-A

130536993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30775836-T-C

130536993-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30775836-T-G

130537348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30776134-G-T

130537391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30776178-G-A

130537425-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30776232-C-G

130537425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30776232-C-T

130537438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30776243-T-C

130537438-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30776243-T-G

130537448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30776251-G-A

130537448-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30776251-G-C

130537658-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30776373-C-G

130537685-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30776400-A-T

130538066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30776743-A-G

130540608-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30781397-G-T

http://identifiers.org/hco/7/GRCh38#130540609-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#30781398-A-C

130540642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30781419-G-A

130540668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30781441-G-A

130540668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30781441-G-T

130540774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30781524-C-T

130540856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30781605-G-A

130540856-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30781605-G-C

130541102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30781787-G-A

130541159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30781841-G-T

http://identifiers.org/hco/7/GRCh38#130541184-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#30781869-C-A

130541186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30781871-G-A

130541774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30782417-G-T

130541864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30782526-T-C

130541874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30782534-G-A

130541874-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30782534-G-C

130542617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30783086-G-A

130542682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30783131-T-C

http://identifiers.org/hco/7/GRCh38#130542805-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#30783178-A-C

130542805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30783178-A-G

130542976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30783328-G-A

130545084-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30784000-G-T

130545137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30784051-T-C

130545417-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30784277-T-A

130545604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30784475-T-C

130546273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30785174-G-A

130546467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30785344-C-T

http://identifiers.org/hco/7/GRCh38#130546657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#30785537-C-A

130546668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30785548-C-T

130546691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30785571-T-C

130546740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30785618-A-G

130547547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30786359-C-T

130547548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30786360-A-G

http://identifiers.org/hco/7/GRCh38#130547557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#30786369-C-A

130547558-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30786370-T-A

http://identifiers.org/hco/7/GRCh38#130547559-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#30786371-C-A

130547559-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30786371-C-G

130547869-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30786688-G-T

130547887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30786715-T-C

130547893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30786727-T-C

130547933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30786767-T-C

130548033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30786915-T-C

130548161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30787019-G-A

130548285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30787133-A-G

130548904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30787502-C-T

130549019-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30787589-T-A

http://identifiers.org/hco/7/GRCh38#130549271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#30787822-C-A

http://identifiers.org/hco/7/GRCh38#130550013-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#30788071-A-C

130550014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30788072-C-T

130550941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30789116-A-G

http://identifiers.org/hco/7/GRCh38#130551139-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#30789394-C-A

130551139-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30789394-C-G

http://identifiers.org/hco/7/GRCh38#130551404-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#30789853-C-A

http://identifiers.org/hco/7/GRCh38#130552237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#30790527-C-A

130552237-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30790527-C-G

130552734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30791210-G-A

130553318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30791734-T-C

130554014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30792420-C-T

130554175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30792552-C-T

130554430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30792807-T-C

130554432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30792809-A-G

130554985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30793624-T-C

130555121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30793762-T-C

130561269-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30801560-G-T

130561320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30801611-A-G

130561320-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30801611-A-T

http://identifiers.org/hco/7/GRCh38#130561362-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#30801656-C-A

130561611-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30801820-T-G

130561687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30801893-C-T

130563122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30802418-T-C

130563163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30802459-C-T

130563193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30802489-A-G

130563483-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30802660-G-T

http://identifiers.org/hco/7/GRCh38#130563829-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#30802823-C-A

130563876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30802868-G-A

130593464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30816837-G-A

130593475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30816848-T-C

http://identifiers.org/hco/7/GRCh38#130610182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#30834656-C-A

130610182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30834656-C-T

130610202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30834676-G-T

130610275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30834748-T-C

130610562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30835121-T-C

130611255-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30835979-T-A

130611255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30835979-T-C

http://identifiers.org/hco/7/GRCh38#130611402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#30836138-C-A

130611402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30836138-C-T

130612263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30836930-G-A

130612263-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30836930-G-C

130612263-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30836930-G-T

130612367-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30837034-T-A

130612367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30837034-T-C

http://identifiers.org/hco/7/GRCh38#130612493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#30837167-C-A

130612493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30837167-C-T

130612595-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30837249-T-A

130613482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30838245-T-C

http://identifiers.org/hco/7/GRCh38#130613507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#30838267-C-A

130613507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30838267-C-T

http://identifiers.org/hco/7/GRCh38#130613528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#30838287-C-A

130613528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30838287-C-T

130613536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 30838295-T-C

http://identifiers.org/hco/7/GRCh38#130613773-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#30838505-A-C

130613773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30838505-A-G

http://identifiers.org/hco/7/GRCh38#130613816-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#30838547-A-C

http://identifiers.org/hco/7/GRCh38#130617200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#30840680-C-A

130617317-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30840756-G-C

130617561-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30841525-G-T

130618639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30844076-A-G

130618803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30844223-A-G

130619153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30844913-T-C

http://identifiers.org/hco/7/GRCh38#130619327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#30845096-C-A

130619998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30845907-C-T

130620490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30846360-A-G

130620716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30846567-T-C

130622523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30849690-A-G

130622585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30849752-C-T

130622655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30849824-A-G

http://identifiers.org/hco/7/GRCh38#130622707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#30849870-C-A

130622936-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30850103-G-T

http://identifiers.org/hco/7/GRCh38#130623227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#30850363-C-A

130623227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30850363-C-T

130640328-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30852981-T-C

130640328-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30852981-T-G

130640845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30853414-T-C

130641003-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30853582-T-C

130641021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30853599-G-A

130641280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30853692-T-C

130641574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30853929-T-C

130642186-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30854769-A-T

130642351-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30854927-A-T

http://identifiers.org/hco/7/GRCh38#130642376-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#30854952-C-A

130642426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30854999-T-C

130642467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30855038-G-A

http://identifiers.org/hco/7/GRCh38#130642508-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#30855084-C-A

130642602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30855209-T-C

130650300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30860132-G-A

http://identifiers.org/hco/7/GRCh38#130650344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#30860175-C-A

130650406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30860225-T-C

130650492-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30860288-C-G

130650723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30860477-T-C

130651115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30860859-C-T

http://identifiers.org/hco/7/GRCh38#130651156-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#30860908-A-C

http://identifiers.org/hco/7/GRCh38#130652184-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#30861280-A-C

http://identifiers.org/hco/7/GRCh38#130652288-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#30861330-A-C

130652737-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30862397-A-T

130652836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30862482-G-A

130652836-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30862482-G-T

130652848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30862494-A-G

130652981-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30862622-T-A

130652981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30862622-T-C

http://identifiers.org/hco/7/GRCh38#130661435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#30866112-C-A

130661435-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30866112-C-G

130661454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30866131-A-G

http://identifiers.org/hco/7/GRCh38#130661537-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#30866214-A-C

130661615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30866259-G-A

130662107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30866886-G-A

130662243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30866969-C-T

130662389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30867050-T-C

130662954-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30867523-T-A

130663357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30867928-T-C

130663641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30868233-G-A

130663648-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30868240-A-T

130664119-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30868376-A-T

130664144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30868400-T-C

130664254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30868489-A-G

130664280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30868515-T-C

130664311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30869745-C-T

130664457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30869887-G-A

http://identifiers.org/hco/7/GRCh38#130664492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#30869923-C-A

130664762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30870195-T-C

130664869-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30870310-A-T

130665786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30870759-A-G

130665845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30870819-A-G

130666927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 30871860-A-G

http://identifiers.org/hco/7/GRCh38#130666993-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#30871927-C-A

130667106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30872044-T-C

130667188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30872105-A-G

http://identifiers.org/hco/7/GRCh38#130667332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#30872252-C-A

130667332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30872252-C-T

130667342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30872318-T-C

130667445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30872445-T-C

130667571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30872563-G-A

130667571-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30872563-G-T

130667622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30872607-G-A

130667622-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30872607-G-C

130667886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30872901-G-A

130668086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30873114-C-T

130668292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, undefined
orthologous variants: 30873295-T-C

130668292-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron_variant, undefined
orthologous variants: 30873295-T-G

130668360-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2237
most severe consequence: intron variant
orthologous variants: 30873359-G-C