94978338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121161366-G-A

94978338-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121161366-G-C

94978338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121161366-G-T

94978619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121161067-T-C

94979603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121159723-G-A

94979603-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121159723-G-T

94980373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121158955-A-G

94980461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121158868-T-C

94980574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121158755-C-T

http://identifiers.org/hco/1/GRCh38#94980602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#121158728-C-A

94980602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 121158728-C-T

http://identifiers.org/hco/1/GRCh38#94980694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121158634-C-A

94980819-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 121158517-T-A

94980819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 121158517-T-C

94980833-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121158506-T-G

94980961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 121158422-T-C

94980964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 121158419-G-T

94981051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121158333-T-C

94981115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121158287-G-T

http://identifiers.org/hco/1/GRCh38#94981278-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121158111-A-C

94981284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121158106-A-G

94981396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121158021-G-T

94981673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121157322-A-G

94981673-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121157322-A-T

94981676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121157319-T-C

http://identifiers.org/hco/1/GRCh38#94981703-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121157310-C-A

94981703-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121157310-C-G

94981703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121157310-C-T

94981721-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121157294-G-T

94981810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121157252-T-C

94981825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121157237-C-T

94981963-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121156943-G-T

94982454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121156532-A-G

94982769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121155929-T-C

94982786-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121155916-T-A

94982826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121155646-T-C

94982971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121155521-G-A

94982971-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121155521-G-T

94982988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 121155504-T-C

94983102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121155407-A-G

94983158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121155351-T-C

94983251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121155258-A-G

94983260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121155249-G-A

94983308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 121155201-T-C

94983313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 121155188-G-A

94983313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 121155188-G-T

94983346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121155155-A-G

http://identifiers.org/hco/1/GRCh38#94983349-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121155152-A-C

94983368-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121155133-G-T

94983372-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121155129-T-A

94983400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121155102-T-C

94983406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121155099-T-C

94983440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121155067-G-A

94983442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121155065-T-C

94983459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121155052-G-A

94983459-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121155052-G-T

94983460-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121155051-T-A

94983460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121155051-T-C

http://identifiers.org/hco/1/GRCh38#94983469-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#121155042-A-C

94983469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121155042-A-G

94983469-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121155042-A-T

http://identifiers.org/hco/1/GRCh38#94983472-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#121155039-C-A

94983472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121155039-C-T

94983477-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121155034-T-A

94983477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121155034-T-C

94983541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121154970-T-C

94983541-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121154970-T-G

94983542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121154969-C-T

94983586-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121154553-C-G

94983588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121154551-C-T

94983598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121154541-A-G

94984255-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121153930-C-G

94984255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121153930-C-T

94984367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121153827-A-G

94984619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121153590-A-G

94985392-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121153084-T-G

94985609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121152921-T-C

http://identifiers.org/hco/1/GRCh38#94985650-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121152875-A-C

94985920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121152584-G-A

94985949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121152543-A-G

94985972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121152524-T-C

94986120-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121152356-G-C

94986120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121152356-G-T

94986170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121152329-A-G

94986201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121152307-G-A

94986784-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121151671-T-A

94986829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121151628-A-G

94986867-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121151590-C-G

94987117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121150885-T-C

94987216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121150781-C-T

94987224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121150773-T-C

94987233-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121150764-T-G

http://identifiers.org/hco/1/GRCh38#94987845-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121150231-A-C

94988095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121149990-C-T

http://identifiers.org/hco/1/GRCh38#94988111-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121149976-C-A

94989630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121149452-A-G

94989785-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121149307-C-G

94989915-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121149224-G-T

94989975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121149187-T-C

94989976-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121149186-G-C

94990195-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121148983-A-T

94990196-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121148982-C-G

94990301-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121148893-A-T

94990495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121148711-A-G

94990508-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121148698-T-A

94990586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121148640-T-C

94990683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121148412-C-T

94990869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121148259-A-G

94990984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121148144-G-A

94993933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121147109-T-C

94997262-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121144087-C-G

94997262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121144087-C-T

94997589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121143804-C-T

94997612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121143781-G-T

94997958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121143477-G-A

94997964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121143471-G-T

94998084-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121143365-T-G

94998229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121143231-C-T

94998455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121143003-C-T

94998473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121142985-T-C

94998649-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121142843-G-C

94998782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121142722-G-A

94998782-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121142722-G-C

94998852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121142656-G-A

94998854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121142654-G-A

94998907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121142607-G-A

http://identifiers.org/hco/1/GRCh38#94999138-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121142381-A-C

http://identifiers.org/hco/1/GRCh38#94999341-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121141807-C-A

94999341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121141807-C-T

94999352-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121141796-T-A

94999566-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121141586-T-A

94999807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121141220-T-C

95000046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121141000-C-T

95000126-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121140935-C-G

95000127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121140934-T-C

95000169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121140892-T-C

95000592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121140759-G-A

95000735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121140620-T-C

95000777-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121140577-T-A

95000777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121140577-T-C

http://identifiers.org/hco/1/GRCh38#95001011-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121140390-C-A

95001197-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121140219-T-A

http://identifiers.org/hco/1/GRCh38#95001265-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121140161-A-C

http://identifiers.org/hco/1/GRCh38#95002101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121139328-C-A

95002165-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121139269-T-G

95002324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121139121-G-A

95002522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121138847-A-G

95002714-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121138511-C-G

95002789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121138401-G-A

95002839-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121138352-A-T

95003327-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121137819-T-G

95003436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121137719-C-T

95004060-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121137272-T-A

95004163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121137167-A-G

95004206-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 121137123-G-T

http://identifiers.org/hco/1/GRCh38#95004209-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121137120-A-C

95005107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121137020-C-T

95005163-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121136984-T-G

95005182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121136965-C-T

95006867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121136061-C-T

95010491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121134808-C-T

95010569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121134734-A-G

95010995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121134317-C-T

95011330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121134094-A-G

95012472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121133605-C-T

95012593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121133463-G-T

95012631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121133423-C-T

95012727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121133327-A-G

95012819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121133239-T-C

95012819-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121133239-T-G

95013183-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121133176-A-T

95013193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121133166-T-C

95013851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121132844-G-A

95013917-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121132778-T-A

95013917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121132778-T-C

95013978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121132741-C-T

95013979-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121132740-T-G

95015488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121130256-A-G

95015581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121130186-T-C

95015601-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121130166-G-C

95015986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121129839-G-A

95015986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121129839-G-T

95016314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121129530-C-T

95016492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121129420-G-A

95016610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121129325-C-T

95016711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121129229-C-T

95016726-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121129214-G-C

95016744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121129199-C-T

95016754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121129189-A-G

http://identifiers.org/hco/1/GRCh38#95017034-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121128788-C-A

95017339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121128532-C-T

95017348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121128525-A-G

http://identifiers.org/hco/1/GRCh38#95017354-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121128498-C-A

95018855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121127241-T-C

95018876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121127220-T-C

95018949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121127166-T-C

95018951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121127164-A-G

95019056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121127053-T-C

95019183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121126926-C-T

95019416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121126700-A-G

95019490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121126644-T-C

95019523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121126611-A-G

http://identifiers.org/hco/1/GRCh38#95021167-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121125172-A-C

95021167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121125172-A-G

95021209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121125130-C-T

95021226-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121125114-T-G

95021245-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121125095-C-G

http://identifiers.org/hco/1/GRCh38#95021255-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121125085-A-C

95021315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121125025-T-C

95021360-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121124978-A-T

95021493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121124881-C-T

95021495-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121124880-G-T

95021584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121124794-T-C

95021795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121124596-C-T

95022181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121124063-A-G

http://identifiers.org/hco/1/GRCh38#95022359-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121123892-A-C

http://identifiers.org/hco/1/GRCh38#95022360-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121123891-C-A

http://identifiers.org/hco/1/GRCh38#95022505-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121123801-C-A

95022677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121123653-C-T

95022706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121123626-T-C

95022783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121122156-G-A

95022818-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121122122-A-T

95023077-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121121881-T-A

95023570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121121506-T-C

95023664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121121418-A-G

95023929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121121187-C-T

95024000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121121115-T-C

95024114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121121000-G-A

95027037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121113948-A-G

95027041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121113944-T-C

95027089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121113896-G-A

95027315-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121113679-A-T

95034028-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121111494-T-A

95034742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121110778-C-T

95034772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121110746-T-C

95034795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121110683-T-C

95034911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121110412-T-C

95034961-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121110324-C-G

95035554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121109462-A-G

95035823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 121109186-C-T

95035949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121109063-A-G

95036085-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121108908-T-A

http://identifiers.org/hco/1/GRCh38#95036104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121108891-C-A

http://identifiers.org/hco/1/GRCh38#95036905-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121108756-C-A

95036911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121108750-T-C

95036964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121108698-G-A

95037043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121108583-G-A

95037173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121108435-A-G

95037247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121108377-G-A

95037265-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121108359-C-G

95037366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121108175-A-G

95037382-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121108162-T-G

95037396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121108135-C-T

95037607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121107967-G-T

95037849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121107826-T-C

95037883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121107793-C-T

95037943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121107746-C-T

95037948-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121107741-T-G

95039326-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121107326-G-C

95039468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121107207-G-A

95039470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121107205-C-T

95039734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121106236-G-T

95039743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121106227-C-T

95039852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121106135-C-T

95041145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121105619-T-C

95041682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121104223-G-A

95041682-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121104223-G-T

95041733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121104174-G-A

95041733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121104174-G-T

http://identifiers.org/hco/1/GRCh38#95041737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121104170-C-A

95041737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121104170-C-T

http://identifiers.org/hco/1/GRCh38#95041760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121104149-C-A

95041760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121104149-C-T

95041996-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121103949-T-G

95043759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121101248-G-A

95045218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121095615-T-C

95045287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121095542-G-A

95045366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121095460-T-C

95045419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121095405-T-C

95046075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121095242-A-G

95046662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121095024-A-G

95046685-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121095001-A-T

95047109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121094467-A-G

95047126-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121094450-T-G

95048229-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121094025-T-A

95048229-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121094025-T-G

95048246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121094012-G-A

95048382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121093876-T-C

95062133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121092721-T-C

95064754-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121092508-A-T

95064836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121092427-A-G

95064867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 121092404-A-G

http://identifiers.org/hco/1/GRCh38#95065121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121091481-C-A

95065121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121091481-C-T

95065669-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121090979-T-G

95065670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121090978-G-A

95066061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121089386-T-C

95066548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121089228-G-T

95066549-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121089227-A-T

95066599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121089172-G-A

95066676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121089107-G-A

http://identifiers.org/hco/1/GRCh38#95066975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121088955-C-A

95071904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121087091-T-C

95072254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121086132-A-G

95072607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 121085783-T-C

http://identifiers.org/hco/1/GRCh38#95072862-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#121085531-C-A

95072862-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 121085531-C-G

95072862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 121085531-C-T

http://identifiers.org/hco/1/GRCh38#95072893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#121085500-C-A

95072893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121085500-C-T

http://identifiers.org/hco/1/GRCh38#95072906-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#121085488-A-C

95072918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 121085476-G-A

95072918-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 121085476-G-C

95072930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 121085466-G-A

95072930-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28287
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 121085466-G-C