95867095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 93418396-T-C

http://identifiers.org/hco/12/GRCh38#95867207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93418284-C-A

95867207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93418284-C-T

http://identifiers.org/hco/12/GRCh38#95867233-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93418266-A-C

95867233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93418266-A-G

95867234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93418265-G-T

95867240-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93418261-T-G

95869619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 93417552-G-A

95869619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 93417552-G-T

95869828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93417432-T-C

95869843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93417417-A-G

http://identifiers.org/hco/12/GRCh38#95869906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93417356-C-A

95869906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93417356-C-T

95869935-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93417336-T-A

95869974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93417298-C-T

95870251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93417121-T-C

95870285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93417087-A-G

95870303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93417074-T-C

95870303-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93417074-T-G

95870305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93417072-T-C

95870410-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93417019-A-T

95870440-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93416999-T-G

95871661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93416283-G-A

95872116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93415964-G-A

95872116-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93415964-G-T

95872153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93415935-G-T

95872185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93415901-G-A

95872185-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93415901-G-T

95872192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93415894-T-C

95872297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 93415785-A-G

95872482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93415594-A-G

95872940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93415343-A-G

95872955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93415328-A-G

95872996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93415240-T-C

95873175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93415063-C-T

95873607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93414647-C-T

95873839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93414421-C-T

95874154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93414113-A-G

95874280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93413909-A-G

95874298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93413884-T-C

95874345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93413835-G-A

95874348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93413832-A-G

95874447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93413732-G-A

95874712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93413483-G-A

95876147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93412529-A-G

95876522-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93412160-C-G

95876522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93412160-C-T

95876799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93411960-A-G

95877728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93411683-A-G

http://identifiers.org/hco/12/GRCh38#95878134-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93411342-C-A

95878134-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93411342-C-G

95878162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93411314-T-C

95878187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93411289-C-T

95878203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 93411273-T-C

95878203-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 93411273-T-G

95879540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93410099-C-T

95879829-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 93409840-T-A

95879829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 93409840-T-C

95879852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 93409827-T-C

95879852-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 93409827-T-G

95879868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 93409811-A-G

95881424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93406829-A-G

http://identifiers.org/hco/12/GRCh38#95881498-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93406766-A-C

95881569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93406691-A-G

95881609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93406655-A-G

http://identifiers.org/hco/12/GRCh38#95881636-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93406628-C-A

95881636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93406628-C-T

95881639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93406625-T-C

http://identifiers.org/hco/12/GRCh38#95888058-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93406158-A-C

95888058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93406158-A-G

95888118-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93406102-T-G

95888235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93406024-G-A

95888265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93405990-A-G

http://identifiers.org/hco/12/GRCh38#95888347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93405909-C-A

95888367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93405889-A-G

95888371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93405885-G-T

95888407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93405848-G-A

95888407-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93405848-G-T

95888521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93405721-C-T

95888547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93405694-G-A

95888547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93405694-G-T

http://identifiers.org/hco/12/GRCh38#95888590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93405650-C-A

95888646-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93405610-T-A

95888794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93405031-T-C

95888854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93404968-T-C

95888925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93404894-G-A

95888925-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93404894-G-T

http://identifiers.org/hco/12/GRCh38#95888941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93404878-C-A

95888941-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93404878-C-G

95888941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93404878-C-T

95888947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93404872-G-A

95888947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93404872-G-T

95888951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93404868-A-G

http://identifiers.org/hco/12/GRCh38#95888985-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93404839-A-C

95888985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93404839-A-G

95888985-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93404839-A-T

95888995-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93404837-T-G

http://identifiers.org/hco/12/GRCh38#95889011-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93404830-C-A

95889011-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93404830-C-G

95889011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93404830-C-T

http://identifiers.org/hco/12/GRCh38#95889017-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93404826-A-C

95889017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93404826-A-G

95889017-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93404826-A-T

95889034-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93404809-T-A

95889034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93404809-T-C

http://identifiers.org/hco/12/GRCh38#95889419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93404524-C-A

95889637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93404311-A-G

95890697-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93403749-G-T

http://identifiers.org/hco/12/GRCh38#95890698-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93403748-C-A

95890698-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93403748-C-G

95890698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93403748-C-T

http://identifiers.org/hco/12/GRCh38#95890732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93403705-C-A

95890732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93403705-C-T

95890794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93403634-G-A

95890794-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93403634-G-T

95890855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron_variant, missense_variant
orthologous variants: 93403594-G-A

95890855-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron_variant, missense_variant
orthologous variants: 93403594-G-C

95890855-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron_variant, missense_variant
orthologous variants: 93403594-G-T

95890873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron_variant, missense_variant
orthologous variants: 93403581-G-A

95890873-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron_variant, missense_variant
orthologous variants: 93403581-G-C

95890873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron_variant, missense_variant
orthologous variants: 93403581-G-T

95890904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron_variant, missense_variant
orthologous variants: 93403550-C-T

http://identifiers.org/hco/12/GRCh38#95890905-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93403549-C-A

95890905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 93403549-C-T

95890953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93403501-A-G

95891012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93403416-G-A

95891012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93403416-G-T

95891025-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93403403-G-T

95891198-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93403282-G-T

95892899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93402698-C-T

95893008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93402538-A-G

95893188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93402377-T-C

95894991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron_variant, missense_variant, splice_region_variant
orthologous variants: 93401803-G-A

95894991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron_variant, missense_variant, splice_region_variant
orthologous variants: 93401803-G-T

http://identifiers.org/hco/12/GRCh38#95895089-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93401711-C-A

95895181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93401624-T-C

95895287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93401547-T-C

95895292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93401542-G-A

95895292-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93401542-G-C

95896285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93401005-C-T

95896373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93400908-G-A

http://identifiers.org/hco/12/GRCh38#95896389-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93400898-A-C

95896442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 93400858-A-G

http://identifiers.org/hco/12/GRCh38#95896476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93400804-C-A

95896529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 93400758-G-A

95896529-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 93400758-G-T

95896539-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 93400748-G-T

95896570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 93400720-G-T

http://identifiers.org/hco/12/GRCh38#95896584-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93400706-A-C

http://identifiers.org/hco/12/GRCh38#95896619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93400697-C-A

http://identifiers.org/hco/12/GRCh38#95896696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93400628-C-A

95896696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93400628-C-T

95896732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93400601-C-T

95896734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93400599-C-T

http://identifiers.org/hco/12/GRCh38#95896768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93400569-C-A

95898011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93399458-G-A

http://identifiers.org/hco/12/GRCh38#95898198-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93399311-A-C

95898439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 93399091-A-G

95898479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 93399051-A-G

95898624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 93398698-C-T

95898640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 93398682-A-G

95898734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 93398588-A-G

95898741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 93398581-T-C

95898839-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93398461-C-G

95898839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93398461-C-T

95898888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93398425-G-A

95898888-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93398425-G-C

95898888-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93398425-G-T

95899085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93397962-A-G

95899101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93397946-C-T

95903883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93393871-G-A

95903883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93393871-G-T

http://identifiers.org/hco/12/GRCh38#95903998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93393802-C-A

95904256-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93393482-T-A

95904256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93393482-T-C

95904352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93393407-C-T

95904375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93393384-G-A

95904379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93393380-G-A

95904564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93393010-C-T

95904577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93392997-A-G

95904785-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93392815-A-T

95904871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93392757-T-C

95905102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93392654-C-T

95905308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93392628-G-A

95905311-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93392625-A-T

95905379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93392549-C-T

95905414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93392513-G-A

http://identifiers.org/hco/12/GRCh38#95905440-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93392487-A-C

95905450-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93392477-C-G

95905450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93392477-C-T

95905536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93392389-T-C

95905556-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93392369-T-A

95905714-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93392217-G-C

95905720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93392211-T-C

95905811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93392123-T-C

95905830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93392107-C-T

95905929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93391915-T-C

http://identifiers.org/hco/12/GRCh38#95906024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93391794-C-A

95906024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93391794-C-T

95906091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93391727-T-C

95906250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93391579-A-G

95906250-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93391579-A-T

http://identifiers.org/hco/12/GRCh38#95906251-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93391578-A-C

95906251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93391578-A-G

95906258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93391571-A-G

95906412-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: missense variant
orthologous variants: 93391418-T-A

95906412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: missense variant
orthologous variants: 93391418-T-C

95906430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 93391400-A-G

95913147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93391016-G-T

95913168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93390994-C-T

95913510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93390765-G-A

95913529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93390745-G-A

95913542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93390732-A-G

95913593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93390680-G-A

95913813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93390457-T-C

http://identifiers.org/hco/12/GRCh38#95913907-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93390375-C-A

95913907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93390375-C-T

95913933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93390351-G-A

95913981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93390303-A-G

95914037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93390251-C-T

95915628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93389154-G-A

95915642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93389140-A-G

95915694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93389088-G-A

95915907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93388952-C-T

95916067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93388799-T-C

95917337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93385977-A-G

95917425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93385904-T-C

95917426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93385903-C-T

http://identifiers.org/hco/12/GRCh38#95917718-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93385826-A-C

http://identifiers.org/hco/12/GRCh38#95918015-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93385634-C-A

95918015-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93385634-C-G

95918364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93385345-A-G

95918533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93385177-G-A

95918586-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron_variant, undefined
orthologous variants: 93385124-G-T

95918754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron_variant, undefined
orthologous variants: 93384996-G-A

95918754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron_variant, undefined
orthologous variants: 93384996-G-T

95918756-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron_variant, undefined
orthologous variants: 93384994-G-T

http://identifiers.org/hco/12/GRCh38#95918758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#93384992-C-A

95918758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron_variant, undefined
orthologous variants: 93384992-C-T

95918776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron_variant, undefined
orthologous variants: 93384983-A-G

95918776-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron_variant, undefined
orthologous variants: 93384983-A-T

http://identifiers.org/hco/12/GRCh38#95918784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#93384975-C-A

http://identifiers.org/hco/12/GRCh38#95918795-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#93384950-C-A

95918795-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron_variant, undefined
orthologous variants: 93384950-C-G

95918795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron_variant, undefined
orthologous variants: 93384950-C-T

95918847-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93384898-T-G

95919028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93384627-G-A

95919028-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93384627-G-T

95919070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93384586-G-A

95919078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93384578-G-A

95936416-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93381427-T-G

95936456-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93381382-G-T

95936458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93381380-T-C

95936563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93381275-T-C

95940575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93379389-T-C

95940731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93379241-G-A

95940731-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93379241-G-C

http://identifiers.org/hco/12/GRCh38#95940900-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93379060-A-C

http://identifiers.org/hco/12/GRCh38#95940902-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93379058-A-C

95940902-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93379058-A-T

95940961-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93378998-T-A

95940962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93378997-G-A

95941503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93377992-A-G

95941871-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93377620-T-A

95941871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93377620-T-C

95942026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93377471-T-C

95942363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93376725-A-G

95942364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93376724-C-T

95942380-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93376716-G-T

95942512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 93376592-G-A

95942512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 93376592-G-T

95942576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 93376527-T-C

95942732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26843
most severe consequence: intron variant
orthologous variants: 93376421-C-T