http://identifiers.org/hco/5/GRCh38#102604764-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#98241360-A-C

102604767-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98241357-A-T

102604972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98241158-A-G

102605300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98240839-T-C

102605329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98240819-A-G

102605347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98240804-C-T

102605388-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98240763-G-T

102605539-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98240598-T-G

http://identifiers.org/hco/5/GRCh38#102605592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#98240550-C-A

http://identifiers.org/hco/5/GRCh38#102605646-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#98240496-C-A

102605649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98240493-A-G

102605653-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98240489-G-T

102615147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98233037-T-C

102615159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98233025-G-A

102615177-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98233015-T-A

102615182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98233010-T-C

102615529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98232722-C-T

102617457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98231493-A-G

102617487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98231463-C-T

102618255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98230774-G-A

102618255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98230774-G-T

102618456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98230589-T-C

http://identifiers.org/hco/5/GRCh38#102618619-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#98230439-A-C

102618619-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98230439-A-T

http://identifiers.org/hco/5/GRCh38#102618637-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#98230420-C-A

102618644-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98230413-T-A

http://identifiers.org/hco/5/GRCh38#102618682-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#98229917-C-A

102618682-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98229917-C-G

102618859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98229738-T-C

102618861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98229736-T-C

http://identifiers.org/hco/5/GRCh38#102618899-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#98229695-C-A

102618900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98229694-A-G

http://identifiers.org/hco/5/GRCh38#102618942-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#98229656-A-C

http://identifiers.org/hco/5/GRCh38#102618973-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#98229625-A-C

102619082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98229541-G-A

102619082-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98229541-G-T

102619099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98229520-G-A

102619169-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98229451-G-C

102619953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98227785-C-T

102619956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98227782-A-G

102619992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98227727-T-C

102620109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98227630-A-G

102620146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98227596-A-G

102620212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98227523-A-G

102620324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98227427-G-A

102620402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98227351-A-G

102620644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98226989-T-C

102620666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98226966-C-T

http://identifiers.org/hco/5/GRCh38#102620756-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#98226877-C-A

102620821-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98226813-C-G

102620826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98226808-C-T

102620892-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98226747-C-G

102620892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98226747-C-T

http://identifiers.org/hco/5/GRCh38#102620902-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#98226737-C-A

102620966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98226654-A-G

102621015-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98226601-T-G

102621689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98226309-G-A

102621715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98226282-G-A

102621748-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98226246-A-T

102621759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98226235-A-G

102621786-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98226209-C-G

102621972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98226059-C-T

102622257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98211062-T-C

102622518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 98210816-C-T

102622521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 98210814-G-A

102622546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 98210789-T-C

102622645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 98210689-T-C

102622860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98210483-T-C

102622864-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98210479-G-C

102623428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98209767-A-G

102623753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98209446-G-A

102623847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98209352-C-T

102624193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98209018-A-G

102625075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98208170-T-C

102625177-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98208064-G-C

102625202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98208039-T-C

102625350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98207882-T-C

102625504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98207723-T-C

102625611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98207615-G-T

102625632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98207597-A-G

102625699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98207530-T-C

102625716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98207513-C-T

102625813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98207420-A-G

102625964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98207269-G-A

102626317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98206952-T-C

102626711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98206246-T-C

102626736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98206221-T-C

102626823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98206153-T-C

102626869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98206106-C-T

102626954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98206023-C-T

102627021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98205964-T-C

102627029-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98205844-T-G

102627030-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98205843-C-G

102627248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98205571-G-A

102627248-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98205571-G-C

102627415-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98205418-G-C

102627461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98205396-G-A

102627612-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98205246-A-T

102627633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98205225-T-C

102627827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98205022-G-A

102628185-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98204679-C-G

102628373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98204508-A-G

102628676-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98203760-T-G

102628739-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98203695-G-C

http://identifiers.org/hco/5/GRCh38#102628784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#98203651-C-A

102629036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98203433-A-G

102629081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98203389-G-A

http://identifiers.org/hco/5/GRCh38#102629268-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#98203162-C-A

http://identifiers.org/hco/5/GRCh38#102629360-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#98203061-C-A

102629500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98202899-A-G

102629586-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98202826-T-G

102629610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98202802-T-C

102629691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98202588-T-C

http://identifiers.org/hco/5/GRCh38#102629699-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#98202580-A-C

102630245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98202059-A-G

102630272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98201979-T-C

102630337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98201914-G-A

102630673-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98201597-T-G

102635918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98201054-T-C

102636093-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98200899-G-T

102636094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98200898-A-G

102636155-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98200820-T-A

102636172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98200804-T-C

http://identifiers.org/hco/5/GRCh38#102636212-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#98200772-C-A

102636212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98200772-C-T

102636214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98200770-G-A

102636214-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98200770-G-C

102636214-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98200770-G-T

102636219-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98200765-G-T

102636320-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98200666-T-G

102636378-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98200600-G-C

102636401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98200573-C-T

102636410-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98200564-G-T

102636429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98200546-T-C

102636460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98200511-C-T

102636517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98200454-T-C

http://identifiers.org/hco/5/GRCh38#102636529-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#98200442-A-C

102636537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98200434-T-C

102636742-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98200053-T-A

102636787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98199982-T-C

102636830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98199939-C-T

102637163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98199637-T-C

102637176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98199620-C-T

102637216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98199582-G-A

102637280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98199517-T-C

102638408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98197630-T-C

102638485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98197598-A-G

102638489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98197594-G-A

102638828-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98197302-G-T

102638934-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98197210-T-G

102638962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98197184-T-C

102648774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98179735-G-A

102648834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98179674-A-G

102648834-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98179674-A-T

102648998-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98179532-T-G

102649008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98179522-A-G

102649037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98179493-C-T

http://identifiers.org/hco/5/GRCh38#102649038-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#98179492-A-C

102649078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98179453-T-C

102649464-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98179114-T-A

102649464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98179114-T-C

102649935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98178332-G-A

102649936-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98178331-T-G

102649970-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98178297-C-G

102649970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98178297-C-T

http://identifiers.org/hco/5/GRCh38#102650101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#98178164-C-A

102650175-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98178085-G-T

102650251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98178009-G-T

102650279-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98177981-T-G

102650547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98177724-T-C

102650662-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98177539-G-C

102651202-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98177123-C-G

102652882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98169157-A-G

102653178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98168877-T-C

102653178-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98168877-T-G

102653219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98168834-G-A

102653259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98168802-T-C

102653303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98168762-G-A

102653303-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98168762-G-C

102653325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98168740-G-A

102653325-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98168740-G-T

102653955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98158482-T-C

102654513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98157910-T-C

102655093-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98157373-C-G

102655108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98157358-A-G

102656158-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98154033-G-C

102656945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98152971-G-A

102657931-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98150151-G-T

102659091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98148811-G-A

102659091-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98148811-G-T

102662627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98124621-T-C

102662820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98121410-C-T

102663047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98121221-G-A

102663328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98121017-A-G

102663397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98120953-T-C

102663414-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98120942-T-A

102663414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98120942-T-C

102663460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98120895-A-G

102663460-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98120895-A-T

http://identifiers.org/hco/5/GRCh38#102663468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#98120884-C-A

102664099-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98120305-G-C

102665205-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98119234-C-G

102665328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98119114-C-T

102665475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98118959-A-G

102665997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98118459-G-A

102666488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98117990-G-A

102666790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98117687-T-C

102666837-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98117640-T-G

http://identifiers.org/hco/5/GRCh38#102666942-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#98117405-A-C

102667156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98116678-A-G

http://identifiers.org/hco/5/GRCh38#102667273-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#98116568-C-A

102667325-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98116542-T-A

102667392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98116474-G-A

102667464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98116403-T-C

102667481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98116391-C-T

102667485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98116387-A-G

102667576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98116315-C-T

102667759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98116137-C-T

102667996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98115814-G-A

102667996-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98115814-G-C

http://identifiers.org/hco/5/GRCh38#102668002-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#98115808-A-C

102668093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98115672-C-T

102668103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98115662-C-T

102668104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98115661-G-A

102668223-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98115540-A-T

102668241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98115521-A-G

102668241-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98115521-A-T

102668432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98115331-T-C

102668453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98115310-T-C

102668796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98114992-A-G

102668893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98114895-G-A

102670673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98113309-C-T

http://identifiers.org/hco/5/GRCh38#102670711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#98113285-C-A

102670711-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98113285-C-G

102671098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98112892-G-A

102671198-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43428
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98112797-T-A