http://identifiers.org/hco/12/GRCh38#67269364-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#119075966-C-A

67269364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 119075966-C-T

67269441-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 119075889-C-G

67269491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 119075839-T-C

67269491-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 119075839-T-G

67269591-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 119075714-G-C

67269591-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 119075714-G-T

67269595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 119075710-T-C

67269595-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 119075710-T-G

67269700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 119075629-G-T

67270122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119075280-G-A

67270122-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119075280-G-T

67270142-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119075260-G-T

67270153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119075252-G-A

67270153-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119075252-G-C

67270153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119075252-G-T

67270229-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119075178-C-G

67270229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119075178-C-T

67270333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119075077-G-T

67270334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119075076-T-C

http://identifiers.org/hco/12/GRCh38#67270344-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#119075066-A-C

67270344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119075066-A-G

67270362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119075048-A-G

67270497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119074908-T-C

67270641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119074797-T-C

http://identifiers.org/hco/12/GRCh38#67270706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#119074739-C-A

67270706-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119074739-C-G

67270706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119074739-C-T

67270713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119074732-C-T

67270875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119074583-A-G

67271587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119073875-C-T

67271733-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119073765-A-T

67271895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119073498-A-G

67272020-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119073401-T-A

http://identifiers.org/hco/12/GRCh38#67272290-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#119073053-A-C

67272290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119073053-A-G

67272429-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119072928-A-T

67272474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119072893-G-A

67273885-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119071397-A-T

67273928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119071348-G-A

67273975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119071308-T-C

67274245-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119071092-C-G

67274413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119070932-G-A

67274663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119070313-T-C

67276456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119068727-C-T

67277069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119068254-G-A

67277071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119068252-A-G

67277141-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119068182-C-G

67277188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119068135-A-G

67277205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119068117-G-A

67277207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119068115-A-G

67277244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119068079-G-A

67277477-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119067846-C-G

67277597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119067738-A-G

67280026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119065304-A-G

67280411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119064814-A-G

67280503-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119064738-A-T

67280544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119064695-G-A

67280681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119064566-T-C

67280681-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119064566-T-G

67280730-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119064521-A-T

67280845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119064441-C-T

67281518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119063947-A-G

67281743-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119063595-T-A

67281803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119063536-A-G

67284471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119059203-A-G

67284471-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119059203-A-T

http://identifiers.org/hco/12/GRCh38#67292406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#119055866-C-A

67292406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119055866-C-T

67292411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119055861-A-G

67292441-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119055831-A-T

67292482-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119055788-T-G

http://identifiers.org/hco/12/GRCh38#67292549-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#119055729-A-C

67292549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119055729-A-G

http://identifiers.org/hco/12/GRCh38#67292556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#119055722-C-A

67292556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119055722-C-T

67292665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 119055604-A-G

67292823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 119055449-A-G

67292909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 119055435-A-G

http://identifiers.org/hco/12/GRCh38#67292999-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#119055416-C-A

67293115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 119055339-G-T

67293142-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 119055313-T-A

67293142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 119055313-T-C

67293142-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 119055313-T-G

http://identifiers.org/hco/12/GRCh38#67293233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#119055226-C-A

http://identifiers.org/hco/12/GRCh38#67293251-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#119055208-C-A

67293251-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: intron variant
orthologous variants: 119055208-C-G

67293251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: intron variant
orthologous variants: 119055208-C-T

67294477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: intron variant
orthologous variants: 119054275-A-G

http://identifiers.org/hco/12/GRCh38#67294494-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#119054258-A-C

67294516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: intron variant
orthologous variants: 119054240-T-C

67295163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 119053837-G-A

67295163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 119053837-G-T

67295181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119053818-T-C

67295275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119053725-G-A

67295275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119053725-G-T

67295529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119053402-G-A

67297121-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119052862-T-G

67297183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119052802-G-A

67297183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119052802-G-T

67297190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119052796-G-A

67297190-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119052796-G-T

http://identifiers.org/hco/12/GRCh38#67297217-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#119052771-A-C

67297217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119052771-A-G

67297240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119052751-T-C

67297295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119052695-A-G

http://identifiers.org/hco/12/GRCh38#67297340-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#119052672-C-A

67297340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119052672-C-T

67297346-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119052665-G-T

67297357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119052654-G-A

67297357-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119052654-G-C

67297441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 119052576-A-G

67297696-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119052321-T-G

67297716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119052182-A-G

67297716-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119052182-A-T

http://identifiers.org/hco/12/GRCh38#67297765-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#119052134-A-C

67297765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 119052134-A-G

67297772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 119052127-C-T

67297780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 119052119-G-A

67297857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119052042-A-G

67297861-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 119052038-T-G

http://identifiers.org/hco/12/GRCh38#67297869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#119052030-C-A

67297869-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119052030-C-G

67297869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119052030-C-T

67297878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119052022-T-C

67297878-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119052022-T-G

67297924-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119051988-G-C

67297924-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119051988-G-T

67297928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119051984-T-C

67297949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119051963-G-A

67297949-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119051963-G-T

67298201-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119051768-T-G

67298508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119051577-G-A

67298799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119051367-T-C

67298885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119051313-G-A

67298917-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119051283-G-C

67298917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119051283-G-T

67298927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119051273-G-A

67298927-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119051273-G-C

67299744-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119050777-G-T

67299753-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119050771-G-C

67301892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: -T-C

http://identifiers.org/hco/12/GRCh38#67302247-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#119049817-A-C

67302247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119049817-A-G

67302349-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 119049716-G-T

67302511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 119049554-G-A

67302511-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 119049554-G-C

67302511-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 119049554-G-T

http://identifiers.org/hco/12/GRCh38#67302632-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#119049434-A-C

67302642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119049424-A-G

67305178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 119047977-A-G

67305514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 119047641-T-C

67305730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 119047425-G-A

67305757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 119047398-C-T

67305763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 119047392-C-T

67305898-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 119047257-T-A

67306168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 119046987-A-G

67306516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 119046639-G-A

67306546-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 119046609-C-G

67306658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119046501-A-G

http://identifiers.org/hco/12/GRCh38#67306694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#119046472-C-A

67306694-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119046472-C-G

67306878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119046276-G-A

67306951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119046216-T-C

67307342-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119046030-T-A

67307342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119046030-T-C

67308216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119045540-T-C

67308353-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119045419-A-T

67308878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119045284-A-G

http://identifiers.org/hco/12/GRCh38#67309013-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#119045176-A-C

67309078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119045108-G-A

67309122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119045079-C-T

67309190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119045009-T-C

67309777-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119044481-A-T

67309797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119044443-A-G

67309798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 119044442-A-G

67309951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 119044295-G-T

67310014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 119044232-A-G

67310047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 119044199-G-A

67310469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 119043802-T-C

67310553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 119043717-T-C

67310553-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 119043717-T-G

http://identifiers.org/hco/12/GRCh38#67310595-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#119043670-C-A

67310706-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 119043601-C-G

67310798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 119043541-A-G

67310824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 119043516-G-A

67310845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 119043486-C-T

67310945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 119043407-T-C

http://identifiers.org/hco/12/GRCh38#67310957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#119043396-C-A

67311049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 119043302-G-A

67311235-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 119043196-T-A

67311248-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 119043177-G-T

http://identifiers.org/hco/12/GRCh38#67311382-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#119043053-A-C

67311382-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: intron variant
orthologous variants: 119043053-A-T

67311457-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: intron variant
orthologous variants: 119042983-G-T

67311481-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: intron variant
orthologous variants: 119042956-T-G

67311681-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: intron variant
orthologous variants: 119042738-T-G

67312486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: intron variant
orthologous variants: 119039223-G-A

67312486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: intron variant
orthologous variants: 119039223-G-T

http://identifiers.org/hco/12/GRCh38#67312885-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#119038830-C-A

67312898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: 3 prime UTR variant
orthologous variants: 119038818-A-G

67312928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: 3 prime UTR variant
orthologous variants: 119038790-C-T

67313034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: 3 prime UTR variant
orthologous variants: 119038686-G-A

67313034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: 3 prime UTR variant
orthologous variants: 119038686-G-T

http://identifiers.org/hco/12/GRCh38#67313068-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#119038651-C-A

http://identifiers.org/hco/12/GRCh38#67313107-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#119038613-A-C

67313107-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: 3 prime UTR variant
orthologous variants: 119038613-A-T

67313382-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: 3 prime UTR variant
orthologous variants: 119038349-A-T

67313645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: 3 prime UTR variant
orthologous variants: 119038105-T-C

67313715-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: 3 prime UTR variant
orthologous variants: 119038045-T-G

67313719-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: 3 prime UTR variant
orthologous variants: 119038041-G-C

67313861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: 3 prime UTR variant
orthologous variants: 119037915-C-T

67313923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: 3 prime UTR variant
orthologous variants: 119037853-T-C

67314063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: 3 prime UTR variant
orthologous variants: 119037737-C-T

http://identifiers.org/hco/12/GRCh38#67314138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#119037673-C-A

67314195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: 3 prime UTR variant
orthologous variants: 119037614-T-C

67314195-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: 3 prime UTR variant
orthologous variants: 119037614-T-G

http://identifiers.org/hco/12/GRCh38#67314198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#119037611-C-A

67314223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: 3 prime UTR variant
orthologous variants: 119037588-A-G

67314312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: 3 prime UTR variant
orthologous variants: 119037542-T-C

http://identifiers.org/hco/12/GRCh38#67314387-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#119037480-C-A

67314427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: 3 prime UTR variant
orthologous variants: 119037431-G-A

67314520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: 3 prime UTR variant
orthologous variants: 119037348-A-G

67314540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: 3 prime UTR variant
orthologous variants: 119037328-G-A

67314540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: 3 prime UTR variant
orthologous variants: 119037328-G-T

67314607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: 3 prime UTR variant
orthologous variants: 119037263-G-A

67314607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: 3 prime UTR variant
orthologous variants: 119037263-G-T

67314866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: 3 prime UTR variant
orthologous variants: 119037026-A-G

http://identifiers.org/hco/12/GRCh38#67315009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#119036913-C-A

67315063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: 3 prime UTR variant
orthologous variants: 119036879-G-T

67315077-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: 3 prime UTR variant
orthologous variants: 119036862-T-A

http://identifiers.org/hco/12/GRCh38#67315078-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#119036861-C-A

67315138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: 3 prime UTR variant
orthologous variants: 119036797-T-C

67316156-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: 3 prime UTR variant
orthologous variants: 119036125-T-G

67316245-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: 3 prime UTR variant
orthologous variants: 119036059-A-T

67316384-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: 3 prime UTR variant
orthologous variants: 119035889-T-G

67316442-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: 3 prime UTR variant
orthologous variants: 119035844-T-A

67316676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: 3 prime UTR variant
orthologous variants: 119035622-G-A

67316762-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30688
most severe consequence: 3 prime UTR variant
orthologous variants: 119035523-G-T