http://identifiers.org/hco/11/GRCh38#21783145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#50755601-C-A

21783148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50755604-G-A

21783222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50755672-A-G

http://identifiers.org/hco/11/GRCh38#21783276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#50755717-C-A

21783309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50755748-G-A

http://identifiers.org/hco/11/GRCh38#21783343-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#50755775-A-C

21783611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50756091-G-T

http://identifiers.org/hco/11/GRCh38#21783730-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#50756194-A-C

21784046-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50756498-C-G

21784046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50756498-C-T

21784111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50756560-G-A

21799304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50759966-G-A

21799324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50759986-G-T

21799771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50760434-T-C

21799847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50760511-A-G

http://identifiers.org/hco/11/GRCh38#21799913-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#50760576-A-C

21799945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 50760603-T-C

21800026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50760689-A-G

http://identifiers.org/hco/11/GRCh38#21800156-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#50760829-C-A

21800640-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50761672-G-T

21800677-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50761713-C-G

http://identifiers.org/hco/11/GRCh38#21800700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#50761728-C-A

21800823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 50761849-G-T

21801252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50762364-G-A

21801290-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50762466-C-G

21801315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50762492-C-T

21801456-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50762635-G-C

21801695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50762826-G-A

21801893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50762970-T-C

21801935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50763011-C-T

21802112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50763131-A-G

21802129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50763141-C-T

http://identifiers.org/hco/11/GRCh38#21802193-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#50763205-C-A

21802193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50763205-C-T

21806693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50764993-A-G

21809399-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50766171-C-G

21809608-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50765970-T-A

21809758-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50765818-C-G

21809758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50765818-C-T

21809848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50765725-T-C

21809876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50765716-T-C

http://identifiers.org/hco/11/GRCh38#21809967-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#50765652-A-C

21809967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50765652-A-G

21810110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50765540-A-G

21810182-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50765471-G-T

21810318-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50783218-G-C

21810610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50783463-G-A

http://identifiers.org/hco/11/GRCh38#21810611-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#50783464-C-A

21810611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50783464-C-T

21815202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50785278-A-G

21815487-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50785548-T-A

21815491-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50785552-G-T

21815492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50785553-A-G

21815650-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50785702-C-G

21815872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50785894-T-C

21816041-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50786042-C-G

21816041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50786042-C-T

21818052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50786353-A-G

21818053-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50786354-G-C

21818257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 50786546-T-C

21818383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50786674-G-T

21818384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50786675-A-G

21818384-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50786675-A-T

21819611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50788758-G-A

21819660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50788806-T-C

21825321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50792522-A-G

21825331-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50792534-T-G

21825447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50792650-C-T

21825521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50792723-G-T

21825551-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50792743-G-C

21825571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50792763-T-C

21825885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50793037-T-C

http://identifiers.org/hco/11/GRCh38#21826348-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#50793446-A-C

21836627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50828076-A-G

21836673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50828122-A-G

21836683-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50828132-A-T

21836704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50828151-T-C

21836999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50828428-C-T

21837027-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50828536-C-G

21837027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50828536-C-T

21837247-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50828749-T-A

21837331-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50828811-T-A

21839584-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50831825-A-T

21839639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50831879-C-T

21840142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50832326-A-G

21840260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50832429-G-A

21840260-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50832429-G-C

21842029-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50835034-C-G

21842048-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50835051-A-T

21842060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50835063-C-T

21842284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50835316-A-G

21842290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50835322-G-A

21842517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50835530-A-G

21842559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50835572-G-A

21842593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50835614-C-T

21842598-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50835619-C-G

http://identifiers.org/hco/11/GRCh38#21842745-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#50835755-A-C

21842745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50835755-A-G

21842881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 50835915-G-A

21842947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 50835970-C-T

21842981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 50835998-A-G

21842986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 50836003-A-G

http://identifiers.org/hco/11/GRCh38#21843197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#50836225-C-A

21843268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50836306-A-G

21843318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50836355-G-T

21843529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50836535-A-G

21843575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50836582-A-G

21843619-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50836624-T-G

21843642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50836647-G-A

http://identifiers.org/hco/11/GRCh38#21843712-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#50836707-A-C

21843720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50836715-T-C

21843794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50836789-G-A

21843978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50836967-T-C

21844117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50837080-T-C

21844118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50837081-G-T

21844264-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50837212-T-A

21845270-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50838018-C-G

21845549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50838251-C-T

21845967-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50838583-A-T

21857572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50839284-T-C

21857702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50839441-C-T

21857717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50839465-G-T

21857838-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50839557-G-C

21857840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50839559-G-A

21857840-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50839559-G-C

21857843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50839562-G-A

21859526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50841228-G-A

http://identifiers.org/hco/11/GRCh38#21860116-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#50842511-C-A

21860122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50842517-T-C

21860175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50842564-A-G

21860561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50842958-G-A

21860671-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50843066-C-G

21862467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50844037-T-C

21862467-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50844037-T-G

21862497-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50844067-T-A

http://identifiers.org/hco/11/GRCh38#21862542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#50844104-C-A

21867915-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50848634-C-G

21867915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50848634-C-T

21868138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50848863-A-G

21868206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50848924-A-G

21868263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50848980-A-G

21868280-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50848999-C-G

21868280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50848999-C-T

21868548-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50849529-A-T

21868832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50849959-A-G

21868871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50849998-G-A

21868885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50850012-T-C

21869027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50850130-A-G

21869070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50850168-G-A

21869098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50850196-G-A

http://identifiers.org/hco/11/GRCh38#21869733-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#50850880-C-A

21869733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50850880-C-T

21869758-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50850905-A-T

21870126-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50851274-T-G

21874369-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50853276-C-G

21874369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50853276-C-T

21874400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50853314-T-C

http://identifiers.org/hco/11/GRCh38#21874490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#50853407-C-A

21874968-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50853906-G-C

21875482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50854465-G-A

21875684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50856637-A-G

21875861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50856792-G-A

21876951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50857173-G-A

21877028-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50857252-T-G

21877057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50857281-G-T

21877124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50857350-T-C

21877146-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50860773-T-G

21877147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50860774-G-A

21877397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50861018-A-G

21877494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50861271-C-T

21877667-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50861445-T-G

21877711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50861489-G-A

21877864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50861622-C-T

21888784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50863382-A-G

21888980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50863539-G-A

21889469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50864010-T-C

21892357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50865111-A-G

21892386-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50865135-T-C

21892455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50865204-T-C

21892564-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50865306-G-C

21892608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50865350-G-A

21892727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50865469-C-T

21892844-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50865584-C-G

21893347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50866073-G-A

21893371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50866096-C-T

21893483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50866208-T-C

21893505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50866230-A-G

21893568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50866273-G-A

21893774-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50866423-C-G

21893904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50866520-T-C

21893908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50866524-T-C

http://identifiers.org/hco/11/GRCh38#21893962-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#50866574-C-A

21894082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50866686-G-A

21894085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50866689-G-T

21894097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50866701-T-C

21894122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50866726-A-G

http://identifiers.org/hco/11/GRCh38#21894204-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#50866805-A-C

21894401-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50866950-T-A

21894432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50866981-A-G

21895111-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50867653-T-G

http://identifiers.org/hco/11/GRCh38#21895148-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#50867690-A-C

21895818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50869765-C-T

21895840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50869787-C-T

http://identifiers.org/hco/11/GRCh38#21895843-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#50869790-A-C

21896024-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50869961-T-G

21896103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50870041-T-C

21896166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50870103-C-T

21896174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50870111-G-A

21896200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50870137-G-A

21896247-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50870179-G-C

21896303-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50870342-C-G

http://identifiers.org/hco/11/GRCh38#21896341-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#50870449-C-A

21896341-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50870449-C-G

21896462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50870548-G-A

21896765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50870815-C-T

21896950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50870975-C-T

21897011-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50871034-G-C

21897388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50871398-G-A

http://identifiers.org/hco/11/GRCh38#21897450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#50871458-C-A

21897614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50871599-C-T

21897723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50871681-C-T

21897816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50871775-T-C

21897978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50871934-A-G

http://identifiers.org/hco/11/GRCh38#21902897-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#50876269-A-C

21902912-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50876283-A-T

21903077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50876446-G-A

21903266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50876624-C-T

21903295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50876652-G-A

21903423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50876799-A-G

21903606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50876931-C-T

21903640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50876960-T-C

21903790-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50877103-A-T

21903908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50877221-A-G

21903969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50877282-T-C

21903972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50877285-T-C

21904460-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50877544-A-T

21904635-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50877723-G-C

21904696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50877848-C-T

21904828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50878037-G-A

21904974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50878204-G-A

21905002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50878232-G-A

21905002-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50878232-G-T

21905552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50878779-A-G

21906251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50879888-T-C

21906350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50879970-T-C

21906459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50880071-T-C

21906575-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50880182-C-G

21906989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50884339-G-A

21907178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50884524-C-T

21907385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50884715-T-C

21907609-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50884941-A-T

21907617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50884949-G-A

21908178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50893766-G-A

21908291-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50893863-T-G

21908330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50893888-C-T

21908418-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50893976-T-A

21908418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50893976-T-C

http://identifiers.org/hco/11/GRCh38#21908421-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#50893979-C-A

21908421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50893979-C-T

21908923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50894384-G-A

21910649-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50896332-T-A

21910649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50896332-T-C

21911389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50896960-A-G

http://identifiers.org/hco/11/GRCh38#21911601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#50897111-C-A

21911681-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50897191-C-G

http://identifiers.org/hco/11/GRCh38#21911998-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#50897397-A-C

http://identifiers.org/hco/11/GRCh38#21912269-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#50897667-A-C

21912384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50897781-G-T

21914161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50898510-T-C

21914689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50899198-C-T

21914849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50899489-G-A

21914866-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50899506-T-G

21915070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50899690-G-A

21915070-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50899690-G-C

21915085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50899705-C-T

21918712-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50903024-A-T

21918744-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50903051-G-T

21918798-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50903103-A-T

21918844-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50903154-G-T

21918932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50903234-A-G

21919085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50903377-G-A

21919149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50903439-A-G

21919162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50903452-C-T

21919259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50903528-C-T

21919594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50903931-G-A

21919741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50904069-C-T

21919761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50904086-A-G

21919850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50904174-A-G

21919850-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50904174-A-T

21920220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50904542-A-G

21920377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50904699-T-C

21920599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50904909-A-G

http://identifiers.org/hco/11/GRCh38#21920614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#50904920-C-A

21920821-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50905138-G-C

21921023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50905298-A-G

21921055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50905323-A-G

21921055-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50905323-A-T

21923391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50907967-A-G

21923465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50908038-G-A

21923716-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50908278-G-T

21923839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50908356-G-A

http://identifiers.org/hco/11/GRCh38#21923877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#50908385-C-A

21923888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50908396-C-T

21924043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50908555-A-G

http://identifiers.org/hco/11/GRCh38#21925115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#50909570-C-A

21925916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50910972-A-G

21926063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50911075-T-C

21926178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50911159-C-T

21926228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50911209-C-T

21926285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50911264-A-G

21926305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50911284-T-C

21926998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50911881-G-A

21928136-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50913100-T-G

21928158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50913122-A-G

http://identifiers.org/hco/11/GRCh38#21928311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#50913283-C-A

http://identifiers.org/hco/11/GRCh38#21928325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#50913297-C-A

21928400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50913372-C-T

21928456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50913428-A-G

21928612-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50913610-C-G

21928612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50913610-C-T

21928713-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50913706-T-A

21928729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50913721-G-A

21928769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50913756-T-C

21928896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50913886-C-T

21929067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50914046-A-G

21929068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50914047-T-C

21929595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50914501-A-G

http://identifiers.org/hco/11/GRCh38#21929623-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#50914531-C-A

21929623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50914531-C-T

21929661-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50914572-T-A

21929825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50914728-T-C

21929843-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50914746-T-G

http://identifiers.org/hco/11/GRCh38#21935592-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#50915751-A-C

21935592-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50915751-A-T

21935655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50915814-T-C

21935682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50915832-G-A

21935682-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50915832-G-T

21935791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50915932-A-G

21935930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50916070-A-G

21935930-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50916070-A-T

21935932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50916072-C-T

21935992-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50916114-C-G

21936238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50916345-C-T

21936367-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50916407-T-A

21936371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50916411-C-T

21936409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50916448-G-A

21936409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50916448-G-T

21943586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50933066-G-A

http://identifiers.org/hco/11/GRCh38#21943602-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#50933082-A-C

http://identifiers.org/hco/11/GRCh38#21943603-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#50933083-A-C

21943627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50933110-T-C

21943749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50933702-G-A

21943749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50933702-G-T

21943807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50933760-G-A

21943819-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50933772-C-G

21943822-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50933775-A-T

21943875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50933824-C-T

21944048-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50933983-A-T

http://identifiers.org/hco/11/GRCh38#21944180-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#50934116-A-C

21944384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50934311-A-G

21944464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50934392-A-G

21944708-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50934623-T-G

http://identifiers.org/hco/11/GRCh38#21944731-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#50934646-A-C

21945087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50934974-G-A

21945125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50935013-A-G

21945211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50935102-C-T

21945263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50937137-G-A

21945296-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50937170-T-G

21945457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50937289-A-G

21945481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50937313-A-G

21945677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50937494-T-C

21945739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50937547-G-T

21945740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50937548-A-G

21945743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50937551-C-T

21945785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50937589-A-G

21945873-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50937625-G-C

21946030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50937781-G-A

21946476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50937916-G-A

21946476-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50937916-G-C

21946556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50938002-A-G

21946687-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50938136-C-G

21946950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50939109-G-A

http://identifiers.org/hco/11/GRCh38#21947370-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#50939489-A-C

21947427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50939537-G-A

21947826-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50939882-G-C

21947941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50939962-A-G

21947994-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50940010-T-G

21948037-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50940053-C-G

21948104-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50940116-C-G

21948104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50940116-C-T

21948114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50940126-G-T

http://identifiers.org/hco/11/GRCh38#21948142-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#50940156-A-C

21948325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50940328-T-C

21948595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50940589-T-C

21948903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50943478-A-G

21948928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50943504-G-A

21948933-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50943512-T-A

21962118-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50949187-C-G

21962251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50949280-C-T

21962949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50949766-T-C

21962960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50949777-A-G

21962968-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50949784-T-A

21964536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50955520-T-C

21964572-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50955563-C-G

21964572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50955563-C-T

21964659-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50955649-C-G

21964667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50955657-A-G

21964667-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50955657-A-T

21965298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50956971-G-T

21965345-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50957019-T-G

21965351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50957037-G-A

21965704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50957416-T-C

21965813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50957524-C-T

http://identifiers.org/hco/11/GRCh38#21966008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#50957645-C-A

21966106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50957741-C-T

21966146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50957798-G-T

21966149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50957801-C-T

http://identifiers.org/hco/11/GRCh38#21966396-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#50958050-A-C

21966450-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50958103-C-G

21966450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50958103-C-T

http://identifiers.org/hco/11/GRCh38#21966671-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#50958300-A-C

21967046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50958774-C-T

21967081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50958806-G-A

21967081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50958806-G-T

21967209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50958922-A-G

21967383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50959009-A-G

21967469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50959043-G-A

21967564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50959135-T-C

21967870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50959444-G-A

21968024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50959545-C-T

21968193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50959682-G-A

21968397-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50959882-C-G

21968455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50959933-G-A

21968583-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50960072-T-A

21968583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50960072-T-C

21968589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50960078-G-A

21968741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50960230-G-A

21968747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50960252-A-G

21968779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50960284-A-G

21968870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50960366-A-G

21968870-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50960366-A-T

21968909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50960405-G-A

21968944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50960441-C-T

http://identifiers.org/hco/11/GRCh38#21969225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#50960725-C-A

21969308-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50960808-C-G

21969308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50960808-C-T

21969318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50960818-C-T

21969368-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50960868-T-A

21969443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50960942-G-A

21969852-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50961640-C-G

http://identifiers.org/hco/11/GRCh38#21969868-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#50961656-A-C

21969999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50961764-T-C

21970014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50961778-G-A

21970357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50962114-C-T

http://identifiers.org/hco/11/GRCh38#21970440-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#50962197-A-C

21970832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50963166-G-T

http://identifiers.org/hco/11/GRCh38#21970843-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#50963177-C-A

21970938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50963225-G-A

21970947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50963238-T-C

21971033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50963323-A-G

21971054-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50963342-G-T

21971230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50963515-T-C

21973985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50966742-A-G

21974122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50966878-C-T

21974134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50966890-G-A

21974134-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50966890-G-C

21974232-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50966995-G-T

21974421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50967386-A-G

21974438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50967403-A-G

21974441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50967406-G-A

21974454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50967419-A-G

http://identifiers.org/hco/11/GRCh38#21974477-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#50967437-A-C

21974543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50967502-T-C

21974549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50967508-G-A

http://identifiers.org/hco/11/GRCh38#21974555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#50967513-C-A

21974648-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50967609-C-G

21974674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50967635-C-T

21974777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50967734-T-C

21974819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50967781-C-T

21974827-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50967789-G-C

21974994-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50967957-C-G

21974994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50967957-C-T

21975003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50967966-C-T

21975072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50968030-T-C

21975082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50968040-C-T

21975093-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50968051-C-G

21975154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50968106-G-A

21975500-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50968367-C-G

21975560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50968424-T-C

http://identifiers.org/hco/11/GRCh38#21975563-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#50968427-A-C

21975580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50968444-A-G

21975602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50968466-T-C

http://identifiers.org/hco/11/GRCh38#21975757-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#50968618-A-C

21976117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 50968992-T-C

21977012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50969670-A-G

21977075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50969737-G-T

21977364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50970012-G-A

21977879-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50971379-T-G

21978072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50971580-C-T

21978139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50971650-A-G

21979214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50974777-A-G

21979267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50974831-C-T

21979269-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50974833-T-G

21979377-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50974941-T-A

21979459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50975017-T-C

21979573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50975112-T-C

21979573-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50975112-T-G

http://identifiers.org/hco/11/GRCh38#21979600-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#50975116-A-C

21979600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50975116-A-G

21981091-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50975734-G-T

21981209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50975869-A-G

21981260-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50975919-G-T

21981439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50976099-A-G

21981601-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50976258-T-A

21981659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50976299-C-T

21981712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50976340-G-A

21981745-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50976376-C-G

21981811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50978263-C-T

21981823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50978275-C-T

21981856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50978307-A-G

21981939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50978384-G-A

21982147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50978590-T-C

21982351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50978852-T-C

21982351-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50978852-T-G

21982366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50978867-G-A

21982479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50978986-C-T

21982512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50979016-G-T

21982579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50979082-A-G

21982627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50979115-C-T

21982633-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50979122-T-G

21983151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50986329-C-T

21983230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50986407-A-G

21983333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50986510-T-C

http://identifiers.org/hco/11/GRCh38#21983582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#50986761-C-A

http://identifiers.org/hco/11/GRCh38#21983653-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#50986866-A-C

21983828-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50989102-A-T

21983848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50989121-A-G

21983876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50989149-C-T

21984193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50989469-G-A

21984362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50989536-G-A

21984362-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50989536-G-C

21984362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50989536-G-T

21984703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50989847-G-A

21984721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50989865-T-C

21984957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50990888-T-C

21985078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50991003-A-G

http://identifiers.org/hco/11/GRCh38#21985092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#50991018-C-A

21985172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50991079-G-A

21986324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50991278-C-T

21986575-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50991457-C-G

21986672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50991563-A-G

21986676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50991567-G-A

21986731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50991627-T-C

http://identifiers.org/hco/11/GRCh38#21986797-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#50991667-A-C

http://identifiers.org/hco/11/GRCh38#21986800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#50991670-C-A

21986853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50991700-G-A

21986879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50991718-G-A

http://identifiers.org/hco/11/GRCh38#21986947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#50991783-C-A

21986947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50991783-C-T

21986981-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50991814-A-T

21986989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50991821-A-G

21987024-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50991854-A-T

21987042-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50991872-G-C

21987078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50991907-C-T

21987161-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50991979-T-A

http://identifiers.org/hco/11/GRCh38#21987307-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#50992124-C-A

http://identifiers.org/hco/11/GRCh38#21987407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#50992216-C-A

21987460-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50992269-G-C

21987479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50992288-G-A

21987497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50992306-C-T

21987545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50992352-A-G

21987740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50992539-G-A

21987821-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50992623-G-C

http://identifiers.org/hco/11/GRCh38#21987889-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#50992690-C-A

21987889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50992690-C-T

21987897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50992698-G-A

21987897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50992698-G-T

http://identifiers.org/hco/11/GRCh38#21988077-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#50992885-C-A

21988077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50992885-C-T

21988184-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50992994-G-C

21988404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50993184-C-T

21988412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50993192-A-G

http://identifiers.org/hco/11/GRCh38#21988431-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#50993209-A-C

21988487-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50993265-C-G

21988516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50993295-T-C

21988692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 50993602-A-G

21988718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50993631-G-A

21989135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50993776-G-A

21989217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50993849-T-C

21989322-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50993938-C-G

21989330-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50993946-C-G

21989501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50994098-A-G

http://identifiers.org/hco/11/GRCh38#21989516-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#50994113-C-A

21989616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50994268-A-G

21989618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50994270-T-C

21989671-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50994319-A-T

21989919-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50994831-T-G

21990760-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50996717-A-T

21991129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50997076-G-T

21991451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50997307-C-T

21991507-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50997360-T-G

21991579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50997432-C-T

21991744-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50997523-G-T

21991845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50997620-G-A

21991845-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50997620-G-T

http://identifiers.org/hco/11/GRCh38#21991897-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#50997669-C-A

21991912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50997683-T-C

21992080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50997846-C-T

21992151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50997914-G-T

21992258-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50998021-A-T

21992275-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50998062-T-A

21992346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50998391-G-A

21992374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50998461-G-A

21992393-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50998480-T-A

21992435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50998522-A-G

21992522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50998616-A-G

21992779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50998810-T-C

21992891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50998920-A-G

21993023-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50999599-G-C

21993073-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50999637-T-G

21993078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50999642-T-C

21993303-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50999859-T-G

21993652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51004537-G-A

21993739-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51004621-C-G

21993780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51004667-A-G

21993804-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51004699-T-A

21993972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51004847-C-T

21994238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51005317-T-C

http://identifiers.org/hco/11/GRCh38#21994304-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#51005379-C-A

21994331-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51005406-T-A

21994361-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51005438-T-G

21994379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51005454-G-A

21994403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51005491-C-T

http://identifiers.org/hco/11/GRCh38#21994416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#51005504-C-A

21994647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51005715-G-A

21994647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51005715-G-T

21994783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51005816-T-C

21994784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51005817-A-G

21995033-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51006064-A-T

21995097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51006127-A-G

21995486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51006510-C-T

21995782-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51006814-G-C

21995782-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51006814-G-T

22002011-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51006858-A-T

22002026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51006873-A-G

22002094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51006942-A-G

22002140-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51006988-G-T

22002165-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51007020-G-T

http://identifiers.org/hco/11/GRCh38#22002186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#51007038-C-A

22002186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51007038-C-T

22002190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51007042-G-A

http://identifiers.org/hco/11/GRCh38#22002226-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#51007080-A-C

22002288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51007144-G-A

22002398-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51007254-G-C

22002402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51007262-G-A

http://identifiers.org/hco/11/GRCh38#22002883-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#51007721-A-C

22002925-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51007764-C-G

22003047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51007882-G-A

22003122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51007951-C-T

22003180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51007999-G-A

22003196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51008015-G-A

22003259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51008065-G-A

22004239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51008286-G-A

22004275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51008316-C-T

22004641-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51008661-C-G

22004770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51008796-A-G

22004847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51008870-G-A

22004847-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51008870-G-T

22004878-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51008901-G-C

22004878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51008901-G-T

22004966-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51008972-C-G

22006861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51011863-G-A

http://identifiers.org/hco/11/GRCh38#22006898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#51011900-C-A

22006898-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51011900-C-G

22007204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51012210-G-A

22007214-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51012220-A-T

22007846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51012991-C-T

http://identifiers.org/hco/11/GRCh38#22008880-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#51013134-C-A

22008973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51013225-T-C

22011454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51014838-A-G

http://identifiers.org/hco/11/GRCh38#22011510-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#51014891-C-A

22011510-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51014891-C-G

22011510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51014891-C-T

22011580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51014953-C-T

22012017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51015391-A-G

22012143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51015508-G-A

http://identifiers.org/hco/11/GRCh38#22013515-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#51016029-A-C

22013515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51016029-A-G

22013731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51016175-C-T

22013821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51016263-C-T

http://identifiers.org/hco/11/GRCh38#22014038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#51016459-C-A

22014038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51016459-C-T

22014161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51016584-A-G

22014204-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51016619-T-A

22014213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51016628-G-A

22014232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51016640-G-A

22014288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51016674-T-C

22014288-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51016674-T-G

22014389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51016793-A-G

22014525-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51017105-T-A

22014525-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51017105-T-G

22014836-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51017461-T-A

22014840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51017465-G-A

22014840-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51017465-G-C

22014875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51017499-G-T

22023369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51025215-T-C

22023378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51025224-A-G

22023410-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51025255-C-G

22023421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51025279-G-A

22023624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51025478-A-G

22023624-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51025478-A-T

22023655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51025509-A-G

22023752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51025601-A-G

22048213-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51051232-G-C

22048375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51051089-G-A

22048375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51051089-G-T

22048522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51050952-T-C

22048546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51050927-C-T

22048947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51050535-G-T

22049036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51050429-G-A

22062034-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51052524-G-C

22062863-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51053418-A-T

22062986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51053541-G-A

22062986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51053541-G-T

22063162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51053721-A-G

http://identifiers.org/hco/11/GRCh38#22063302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#51053839-C-A

22063432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51053981-C-T

22064024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51054879-T-C