154272688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: 3 prime UTR variant
orthologous variants: 62375965-A-G

154272691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: 3 prime UTR variant
orthologous variants: 62375968-A-G

http://identifiers.org/hco/3/GRCh38#154272701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62375978-C-A

http://identifiers.org/hco/3/GRCh38#154272710-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62375987-A-C

154273650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: 3 prime UTR variant
orthologous variants: 62376694-T-C

154273689-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: 3 prime UTR variant
orthologous variants: 62376759-G-C

154273689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: 3 prime UTR variant
orthologous variants: 62376759-G-T

154275685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: 3 prime UTR variant
orthologous variants: 62377521-C-T

http://identifiers.org/hco/3/GRCh38#154275708-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62377544-A-C

154275740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: 3 prime UTR variant
orthologous variants: 62377572-T-C

http://identifiers.org/hco/3/GRCh38#154275813-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62377645-C-A

154275813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: 3 prime UTR variant
orthologous variants: 62377645-C-T

154275947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: 3 prime UTR variant
orthologous variants: 62377760-G-A

154275947-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: 3 prime UTR variant
orthologous variants: 62377760-G-C

154275947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: 3 prime UTR variant
orthologous variants: 62377760-G-T

http://identifiers.org/hco/3/GRCh38#154275963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62377776-C-A

154276090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 62377894-G-A

154276222-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 62378034-C-G

154276231-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 62378043-T-G

154276361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 62378173-G-T

154276375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62378187-T-C

http://identifiers.org/hco/3/GRCh38#154276397-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62378208-A-C

154276397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62378208-A-G

154276398-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62378209-T-A

http://identifiers.org/hco/3/GRCh38#154276462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62378275-C-A

154276462-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62378275-C-G

154276861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 62378857-A-G

154276873-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 62378869-A-T

154276917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62378913-G-A

154276968-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62378955-T-A

154276968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62378955-T-C

http://identifiers.org/hco/3/GRCh38#154277024-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62379008-A-C

154277488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62379338-A-G

154277528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62379353-A-G

http://identifiers.org/hco/3/GRCh38#154277531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62379356-C-A

154277581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62379403-T-C

154277661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 62379483-A-G

154277694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 62379516-A-G

154277737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62379558-T-C

http://identifiers.org/hco/3/GRCh38#154277765-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62379579-A-C

154277765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62379579-A-G

154277783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62379593-A-G

154280379-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62379994-G-C

154280381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62379996-G-T

154280419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62380031-A-G

http://identifiers.org/hco/3/GRCh38#154280436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62380039-C-A

154280436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62380039-C-T

http://identifiers.org/hco/3/GRCh38#154280544-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62380114-A-C

154280558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62380128-A-G

154280673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 62380243-T-C

154280673-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 62380243-T-G

http://identifiers.org/hco/3/GRCh38#154280730-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62380298-A-C

154280730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 62380298-A-G

154280960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 62380541-G-A

154280960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 62380541-G-T

154281132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 62380935-T-C

http://identifiers.org/hco/3/GRCh38#154281451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62381473-C-A

154282184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 62382176-G-A

154283067-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 62382577-T-A

154283067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 62382577-T-C

154283110-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 62382616-G-T

154283118-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 62382624-T-G

154283159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 62382667-G-A

154283159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 62382667-G-T

154283184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 62382687-T-C

154283215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 62382718-T-C

154283285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 62382789-A-G

http://identifiers.org/hco/3/GRCh38#154283545-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62383001-A-C

154283545-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 62383001-A-T

154283660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 62383100-G-A

154283668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 62383108-G-A

154284120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 62384589-T-C

154284557-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 62384680-T-A

154284557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 62384680-T-C

154284677-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 62384798-A-T

154284724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 62384837-T-C

154284725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 62384838-G-T

154284964-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 62385077-T-A

154284964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 62385077-T-C

154285001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62385114-G-A

154285001-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62385114-G-C

154285045-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62385157-A-T

154285049-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62385161-T-A

154285049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62385161-T-C

154285049-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62385161-T-G

http://identifiers.org/hco/3/GRCh38#154285052-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62385164-C-A

154285052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62385164-C-T

154285063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62385175-A-G

http://identifiers.org/hco/3/GRCh38#154285080-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62385188-A-C

http://identifiers.org/hco/3/GRCh38#154285090-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62385199-C-A

154285090-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62385199-C-G

154285111-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62385221-T-A

154285111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62385221-T-C

http://identifiers.org/hco/3/GRCh38#154285119-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62385231-C-A

154285455-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62385481-T-G

154288670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62386622-G-A

154288670-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62386622-G-C

http://identifiers.org/hco/3/GRCh38#154288779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62386659-C-A

154288779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62386659-C-T

154288810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62386680-G-A

154288810-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62386680-G-T

154288814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62386684-A-G

154288814-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62386684-A-T

154288824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62386694-G-A

154288824-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62386694-G-T

154288836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62386706-A-G

154288836-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62386706-A-T

154288837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62386707-G-T

http://identifiers.org/hco/3/GRCh38#154288910-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62386785-A-C

http://identifiers.org/hco/3/GRCh38#154288941-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62386816-A-C

154288941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 62386816-A-G

154288985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62386855-T-C

154289002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62386885-T-C

154289860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62388367-A-G

154289864-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62388371-A-T

http://identifiers.org/hco/3/GRCh38#154289907-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62388416-C-A

154289907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62388416-C-T

154291753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62389704-T-C

154291772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62389723-G-A

154291772-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62389723-G-C

154291870-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62390195-T-A

154291870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62390195-T-C

154291941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62390262-T-C

154292038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62390358-G-A

http://identifiers.org/hco/3/GRCh38#154292428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62391444-C-A

154292428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62391444-C-T

154292544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 62391545-A-G

154292553-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 62391554-T-G

http://identifiers.org/hco/3/GRCh38#154292763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62391734-C-A

154292763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: 62391734-C-T

154292822-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: 62391797-T-A

154292822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: 62391797-T-C

154292916-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: 62391889-G-T

154293005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: 62391959-C-T

154293147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: 62392095-A-G

http://identifiers.org/hco/3/GRCh38#154293184-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62392131-A-C

154293186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: 62392133-T-C

154293195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: 62392142-G-A

http://identifiers.org/hco/3/GRCh38#154293792-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62392420-A-C

http://identifiers.org/hco/3/GRCh38#154293892-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62392505-A-C

154294030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: 62392616-T-C

154294120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: 62392700-T-C

154294420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: 62392960-A-G

154294450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: 62392991-T-C

154294540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: 62393069-C-T

http://identifiers.org/hco/3/GRCh38#154295149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62393510-C-A

154295234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: 62394386-A-G

154295241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: 62394393-C-T

154295253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: 62394405-T-C

154295280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: 62394427-A-G

154295376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: 62394517-G-A

154295376-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: 62394517-G-C

http://identifiers.org/hco/3/GRCh38#154295394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62394535-C-A

154295394-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: 62394535-C-G

154295394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: 62394535-C-T

154295658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: 62394700-C-T

154299682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: 62395296-A-G

http://identifiers.org/hco/3/GRCh38#154299683-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62395297-A-C

154299690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: 62395304-T-C

154299777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: 62395404-C-T

http://identifiers.org/hco/3/GRCh38#154299801-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62395512-A-C

154299801-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: 62395512-A-T

154299990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: 62395696-G-A

154299990-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: 62395696-G-T

http://identifiers.org/hco/3/GRCh38#154300006-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62395712-C-A

154300006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: 62395712-C-T

154300522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: 62395896-G-A

154300522-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: 62395896-G-C

154300522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: 62395896-G-T

154300539-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: 62395913-G-C

154300539-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: 62395913-G-T

154300549-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: 62395926-T-A

154300755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: 62396124-A-G

http://identifiers.org/hco/3/GRCh38#154300760-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62396129-A-C

http://identifiers.org/hco/3/GRCh38#154300852-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62396216-C-A

154300868-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: 62396233-A-T

154300994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: stop gained
orthologous variants: 62396326-G-A

http://identifiers.org/hco/3/GRCh38#154301153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62396485-C-A

154301153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: 62396485-C-T

154301173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: 62396507-A-G

154301187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: 62396521-T-C

154301743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: 62397033-C-T

154301908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: 62397203-G-T

154302049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: 62397340-G-A

154302049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: 62397340-G-T

154302080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: 62397351-A-G

154302108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: 62397381-G-A

154302234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: 62399396-G-A

154303658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62400060-T-C

154303706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62400098-G-A

154303808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62400177-C-T

154303858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62400219-T-C

154303866-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62400227-T-A

154303913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62400270-T-C

154303932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62400289-G-A

154304040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62400385-C-T

154304108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62400443-T-C

154304274-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62400603-G-C

154304276-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62400605-T-A

154304340-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62400715-C-G

154304383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62400750-A-G

154304566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62400921-T-C

http://identifiers.org/hco/3/GRCh38#154305008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62401364-C-A

154305008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62401364-C-T

154305072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62401603-T-C

154305120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 62401791-G-A

154305178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62401849-A-G

154305219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62401892-T-C

154305280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62401922-T-C

154305399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: 62402019-T-C

http://identifiers.org/hco/3/GRCh38#154305405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62402025-C-A

154305405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: 62402025-C-T

154306102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: 62402762-T-C

154306174-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: 62402823-T-A

154306174-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: 62402823-T-G

154306221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: synonymous variant
orthologous variants: 62402884-G-A

http://identifiers.org/hco/3/GRCh38#154306367-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62403029-C-A

154306367-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: 62403029-C-G

154306367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: 62403029-C-T

154306419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: 62403079-G-A

154306419-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: 62403079-G-C

154306419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: 62403079-G-T

154306446-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: 62403106-A-T

154306450-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: 62403110-T-A

154306546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: 62403224-G-A

154306703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: 62403386-T-C

http://identifiers.org/hco/3/GRCh38#154309204-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62403722-A-C

154309204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: 62403722-A-G

154309538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: 62404035-T-C

154309563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: 62404060-T-C

http://identifiers.org/hco/3/GRCh38#154309603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62404101-C-A

154309603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: 62404101-C-T

154309637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: 62404135-T-C

154309644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: 62404141-A-G

http://identifiers.org/hco/3/GRCh38#154309834-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62404331-A-C

154309834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62404331-A-G

154311126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62405053-G-A

154311657-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 62405532-C-G

http://identifiers.org/hco/3/GRCh38#154311860-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62405660-C-A

154311953-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62405693-A-T

http://identifiers.org/hco/3/GRCh38#154312001-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62405726-C-A

154312001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62405726-C-T

154312013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62405736-T-C

154312018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62405741-T-C

154312210-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62405899-G-C

154312210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62405899-G-T

http://identifiers.org/hco/3/GRCh38#154312232-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62405917-C-A

154312232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62405917-C-T

http://identifiers.org/hco/3/GRCh38#154312391-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62406065-C-A

154312500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: 62406142-T-C

http://identifiers.org/hco/3/GRCh38#154312517-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62406159-A-C

154312918-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: 62406244-G-T

154312925-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: 62406251-G-C

154312925-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: 62406251-G-T

http://identifiers.org/hco/3/GRCh38#154313934-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62407303-A-C

154313934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: 62407303-A-G

154314244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: 62407561-C-T

http://identifiers.org/hco/3/GRCh38#154314259-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62407572-A-C

154314290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: 62407602-T-C

154314332-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: 62407632-T-A

154314494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron variant
orthologous variants: 62407747-T-C

154314786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62408029-T-C

154315021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62408226-A-G

154315157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 62408366-G-A

154315157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 62408366-G-T

154315190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 62408399-T-C

154315235-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 62408444-G-C

http://identifiers.org/hco/3/GRCh38#154315265-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62408474-A-C

154315370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62408570-A-G

154315378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62408578-G-T

154315397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62408597-T-C

154315398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62408598-T-C

154315412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62408603-T-C

154315424-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62408611-G-T

154315444-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62408631-A-T

154315701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62408871-C-T

154315725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62408895-G-A

154315906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62409211-A-G

http://identifiers.org/hco/3/GRCh38#154316086-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62409442-A-C

154316086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 62409442-A-G

154316086-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 62409442-A-T

154316276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62409647-A-G

http://identifiers.org/hco/3/GRCh38#154316665-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62410102-A-C

154317207-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62410542-T-A

154323503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62413609-C-T

154324273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: synonymous variant
orthologous variants: 62414238-G-A

154324273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: synonymous variant
orthologous variants: 62414238-G-T

154324367-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: missense variant
orthologous variants: 62414311-C-G

154324367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: missense variant
orthologous variants: 62414311-C-T

154324386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: missense variant
orthologous variants: 62414330-G-A

154324386-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: missense variant
orthologous variants: 62414330-G-C

154324396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: synonymous variant
orthologous variants: 62414340-C-T

http://identifiers.org/hco/3/GRCh38#154324421-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62414365-C-A

154324421-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: 5 prime UTR variant
orthologous variants: 62414365-C-G

154324421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14410
most severe consequence: 5 prime UTR variant
orthologous variants: 62414365-C-T