http://identifiers.org/hco/9/GRCh38#137460175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#24944011-C-A

137460179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 24944007-G-A

137460179-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 24944007-G-C

137460179-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 24944007-G-T

http://identifiers.org/hco/9/GRCh38#137460262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#24943938-C-A

137460262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 24943938-C-T

137460445-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24943712-G-C

137460521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24943641-G-A

137460603-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24943553-G-T

137460620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24943522-G-A

137460620-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24943522-G-T

137460678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24943464-A-G

137460678-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24943464-A-T

http://identifiers.org/hco/9/GRCh38#137460693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#24943449-C-A

137460693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24943449-C-T

137460779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24943361-A-G

137460786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24943354-G-A

137460786-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24943354-G-C

137460786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24943354-G-T

137460827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24943317-A-G

137460878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24943277-G-A

137460878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24943277-G-T

http://identifiers.org/hco/9/GRCh38#137460982-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#24943171-C-A

137460982-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24943171-C-G

137460982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24943171-C-T

http://identifiers.org/hco/9/GRCh38#137460985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#24943168-C-A

137460985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24943168-C-T

137461061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24943066-A-G

137461061-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24943066-A-T

137461101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24943016-A-G

137461184-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24942945-G-T

137461198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24942929-G-A

137461198-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24942929-G-C

137461198-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24942929-G-T

http://identifiers.org/hco/9/GRCh38#137461218-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#24942909-A-C

137461218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24942909-A-G

137461218-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24942909-A-T

137461267-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24942905-G-C

137461267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24942905-G-T

137461315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24942854-G-A

137461315-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24942854-G-T

137461319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24942850-G-A

137461319-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24942850-G-T

137461326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24942843-G-A

137461326-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24942843-G-C

137461326-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24942843-G-T

137461369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24942800-G-A

137461369-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24942800-G-T

http://identifiers.org/hco/9/GRCh38#137461375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#24942794-C-A

137461375-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24942794-C-G

137461375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24942794-C-T

137461388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24942772-T-C

137461388-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24942772-T-G

http://identifiers.org/hco/9/GRCh38#137461568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#24942615-C-A

137461568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24942615-C-T

http://identifiers.org/hco/9/GRCh38#137461685-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#24942514-C-A

137461685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24942514-C-T

http://identifiers.org/hco/9/GRCh38#137461995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#24942364-C-A

137461995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24942364-C-T

137462068-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24942293-G-T

http://identifiers.org/hco/9/GRCh38#137462125-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#24942242-C-A

137462125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 24942242-C-T

137462129-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 24942238-C-G

137462160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24942213-G-A

137462160-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24942213-G-T

http://identifiers.org/hco/9/GRCh38#137462347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#24942032-C-A

137462490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24941935-T-C

137462541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24941891-G-T

137462547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24941885-G-A

137462547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24941885-G-T

137462590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24941843-G-A

137462590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24941843-G-T

137462755-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24941689-T-A

137463002-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24941384-G-T

137463084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 24941312-G-A

137463084-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 24941312-G-C

137463084-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 24941312-G-T

http://identifiers.org/hco/9/GRCh38#137463207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#24941191-C-A

137463207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 24941191-C-T

137463258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24941142-G-T

137463338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24941062-A-G

137463468-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24940928-T-A

137463492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24940904-G-A

137463492-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24940904-G-T

137463587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24940800-G-T

137463624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24940758-A-G

137463638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24940734-T-C

http://identifiers.org/hco/9/GRCh38#137463646-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#24940721-C-A

137463646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24940721-C-T

137463679-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24940681-G-T

137464011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24940425-T-C

137464078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24940381-C-T

137464219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24940243-G-A

137464220-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24940242-G-C

137464231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24940233-A-G

137464268-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24940194-G-C

137464292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24940168-G-A

137464292-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24940168-G-C

137464295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24940165-G-T

137464355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 24940110-C-T

137464462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 24940003-G-A

137464480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24939986-A-G

137464511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 24939954-C-T

http://identifiers.org/hco/9/GRCh38#137464560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#24939898-C-A

137464560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24939898-C-T

137464585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24939866-G-A

137464585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24939866-G-T

137464612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24939848-A-G

137464666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24939802-C-T

http://identifiers.org/hco/9/GRCh38#137464694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#24939771-C-A

137464706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24939758-T-C

137465933-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24938856-T-G

137466006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24938782-G-A

137466188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24938602-G-A

137467306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24937785-T-C

137467307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24937784-G-A

137467399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24937692-G-A

http://identifiers.org/hco/9/GRCh38#137478021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#24932236-C-A

137478021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24932236-C-T

137478091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24932160-A-G

137478091-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24932160-A-T

137478148-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24932103-T-A

137478148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24932103-T-C

137478182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24932067-T-C

137478182-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24932067-T-G

137478218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24932022-G-T

http://identifiers.org/hco/9/GRCh38#137478220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#24932020-C-A

137478220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24932020-C-T

http://identifiers.org/hco/9/GRCh38#137478262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#24931951-C-A

137478262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24931951-C-T

137478266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24931947-A-G

137478266-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24931947-A-T

http://identifiers.org/hco/9/GRCh38#137478289-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#24931852-C-A

137478289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24931852-C-T

137478301-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24931840-C-G

137478301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24931840-C-T

http://identifiers.org/hco/9/GRCh38#137478322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#24931785-C-A

137478322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24931785-C-T

137478460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24931671-C-T

137478465-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24931666-T-A

137478465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24931666-T-C

137478533-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24931587-G-T

http://identifiers.org/hco/9/GRCh38#137478609-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#24931515-A-C

137478612-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24931512-T-A

137478612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24931512-T-C

137478637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24931477-G-A

137478687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24931420-A-G

137478687-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24931420-A-T

137478755-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24931382-G-T

137478894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 24931295-G-A

137478966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 24931236-G-A

137478966-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 24931236-G-C

137478966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 24931236-G-T

137478978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 24931224-G-A

137478978-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 24931224-G-C

137478978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 24931224-G-T

137479006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 24931195-G-A

137479006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 24931195-G-T

http://identifiers.org/hco/9/GRCh38#137479048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#24931146-C-A

137479048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant, undefined
orthologous variants: 24931146-C-T

http://identifiers.org/hco/9/GRCh38#137479051-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#24931143-C-A

137479091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 24931103-G-A

137479091-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 24931103-G-T

137479093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 24931101-G-A

137479093-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 24931101-G-C

137479093-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 24931101-G-T

http://identifiers.org/hco/9/GRCh38#137479239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_acceptor_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#24930955-C-A

137479239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_acceptor_variant, undefined
orthologous variants: 24930955-C-T

http://identifiers.org/hco/9/GRCh38#137479317-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#24930872-A-C

137479317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24930872-A-G

137479354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24930804-T-C

137479378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24930779-C-T

137479461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24930700-A-G

http://identifiers.org/hco/9/GRCh38#137479471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#24930676-C-A

137479557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24930586-G-A

137479557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24930586-G-T

137479563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24930580-A-G

137479587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24930557-T-C

137479588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24930556-A-G

137479589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24930555-C-T

137479757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24930376-A-G

137479811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24930321-T-C

137479863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24930267-C-T

137479923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24930189-C-T

137480173-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24929875-G-C

137480173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24929875-G-T

137480185-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24929863-T-A

137480185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24929863-T-C

137480208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24929859-T-C

137480252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24929822-G-A

137480252-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24929822-G-T

137480322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24929771-G-A

137480322-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24929771-G-C

137480750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron variant
orthologous variants: 24929110-T-C

137480809-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron variant
orthologous variants: 24929067-T-G

137480815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron variant
orthologous variants: 24929061-G-T

137484715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24919538-G-A

137484715-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24919538-G-T

http://identifiers.org/hco/9/GRCh38#137484753-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#24919494-C-A

137484753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24919494-C-T

137484795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24919441-G-T

137486507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24915447-C-T

137492179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24912405-G-A

137492199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24912385-G-A

137493138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24911892-A-G

137493151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24911879-G-T

137493165-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24911873-G-T

http://identifiers.org/hco/9/GRCh38#137493183-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#24911860-C-A

137493183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24911860-C-T

http://identifiers.org/hco/9/GRCh38#137493191-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#24911852-C-A

137493191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24911852-C-T

http://identifiers.org/hco/9/GRCh38#137493214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#24911829-C-A

137493214-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24911829-C-G

137493225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24911806-A-G

http://identifiers.org/hco/9/GRCh38#137493228-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#24911803-A-C

137493228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24911803-A-G

137494926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24909610-C-T

http://identifiers.org/hco/9/GRCh38#137494946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#24909585-C-A

137494946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24909585-C-T

http://identifiers.org/hco/9/GRCh38#137494978-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#24909563-C-A

137494978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24909563-C-T

137495091-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 24909469-G-T

137495153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 24909407-A-G

137495155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24909404-A-G

137495280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24908872-G-A

137497382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24906374-A-G

137497414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24906298-A-G

137497615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24905977-C-T

137498210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24905195-A-G

137498250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 24905155-C-T

137498268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24905137-T-C

http://identifiers.org/hco/9/GRCh38#137498283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#24905113-C-A

137498303-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24905084-G-C

137498307-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24905080-C-G

137498307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24905080-C-T

137498355-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24904994-A-T

137498609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24904780-G-A

137498658-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24904735-G-T

137498722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24904676-C-T

137498736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24904662-C-T

137498802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24904593-G-A

137499026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24904351-C-T

137499218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24904157-A-G

http://identifiers.org/hco/9/GRCh38#137499239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#24904136-C-A

http://identifiers.org/hco/9/GRCh38#137499735-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#24903391-A-C

137499962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24903218-G-A

http://identifiers.org/hco/9/GRCh38#137500925-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#24901465-C-A

137500925-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24901465-C-G

137500925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24901465-C-T

http://identifiers.org/hco/9/GRCh38#137500955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#24901431-C-A

137500955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24901431-C-T

137500959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24901425-G-A

http://identifiers.org/hco/9/GRCh38#137500978-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#24901412-C-A

137500978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24901412-C-T

137500995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24901396-G-A

137500996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24901395-A-G

137500997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24901394-G-A

137500997-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24901394-G-C

137500997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24901394-G-T

137501008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24901383-G-A

137501008-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24901383-G-C

137501008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24901383-G-T

137501085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24901275-C-T

137501145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24901237-C-T

137501521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24900923-G-A

137501521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24900923-G-T

http://identifiers.org/hco/9/GRCh38#137501532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#24900912-C-A

137501532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24900912-C-T

http://identifiers.org/hco/9/GRCh38#137501538-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#24900906-C-A

137501538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24900906-C-T

137501559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24900885-G-A

137501559-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24900885-G-C

http://identifiers.org/hco/9/GRCh38#137501563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#24900881-C-A

http://identifiers.org/hco/9/GRCh38#137501580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#24900876-C-A

137501580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24900876-C-T

http://identifiers.org/hco/9/GRCh38#137501588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#24900868-C-A

137501588-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24900868-C-G

137501588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24900868-C-T

137501618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24900838-G-T

137501753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24900694-A-G

http://identifiers.org/hco/9/GRCh38#137501786-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#24900662-A-C

137501854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24900603-C-T

http://identifiers.org/hco/9/GRCh38#137501878-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#24900580-C-A

137501878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24900580-C-T

137501890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24900576-G-A

137501891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24900575-G-A

137505776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24892883-G-A

137505776-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24892883-G-C

http://identifiers.org/hco/9/GRCh38#137505780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#24892879-C-A

137505780-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24892879-C-G

137505780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24892879-C-T

137505851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24892838-G-A

137505851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24892838-G-T

http://identifiers.org/hco/9/GRCh38#137505969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#24892743-C-A

137505969-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24892743-C-G

137505969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24892743-C-T

137506087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 24892621-C-T

137506091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 24892617-C-T

137515200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24888965-G-A

137515200-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24888965-G-C

137515259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24888897-G-A

137515259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24888897-G-T

http://identifiers.org/hco/9/GRCh38#137515276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#24888881-C-A

137515276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24888881-C-T

http://identifiers.org/hco/9/GRCh38#137515278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#24888879-C-A

137515278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24888879-C-T

137515297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24888849-G-A

137515297-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24888849-G-C

137515297-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24888849-G-T

137515342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24888800-G-A

137515342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24888800-G-T

http://identifiers.org/hco/9/GRCh38#137515366-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#24888782-C-A

137515366-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24888782-C-G

137515366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24888782-C-T

http://identifiers.org/hco/9/GRCh38#137515403-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#24888745-C-A

137515403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24888745-C-T

http://identifiers.org/hco/9/GRCh38#137515412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#24888736-C-A

137515412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24888736-C-T

137515465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24888686-G-A

137515465-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24888686-G-C

137515465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24888686-G-T

http://identifiers.org/hco/9/GRCh38#137515536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#24888617-C-A

137515536-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24888617-C-G

137515536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24888617-C-T

137515639-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24888519-T-A

137515655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24888509-G-A

137515655-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24888509-G-C

137515655-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24888509-G-T

http://identifiers.org/hco/9/GRCh38#137515661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#24888503-C-A

137515661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24888503-C-T

137515662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24888502-A-G

137519768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24887483-T-C

137519769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24887482-A-G

137519844-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24887432-G-T

137519851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24887423-G-A

137519851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24887423-G-T

137520774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24886700-G-T

137521761-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24886146-C-G

137521761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24886146-C-T

137521829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24886070-G-T

137522221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24885728-C-T

137522572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24885552-T-C

137522625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24885507-A-G

137522690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24885454-C-T

137522754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24885391-G-A

137522754-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24885391-G-C

137522754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24885391-G-T

137522808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24885337-G-A

137522817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24885328-G-A

137522901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24885245-A-G

137522918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24885228-C-T

137522951-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24885197-C-G

137522953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24885195-G-A

137522953-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24885195-G-C

137522953-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24885195-G-T

137522956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24885192-G-A

137522956-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24885192-G-T

137522996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24885156-G-A

137522996-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24885156-G-C

137522996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24885156-G-T

137523015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24885137-G-T

137537895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24878829-C-T

137537900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24878824-C-T

137537907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24878817-G-A

137538058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24878705-C-T

137538180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24878645-T-C

137538192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24878636-G-A

137538289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24878567-G-A

137538467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24878419-G-A

137538479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24878407-A-G

137540588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24877273-G-A

137540588-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24877273-G-C

137540588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24877273-G-T

http://identifiers.org/hco/9/GRCh38#137540591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#24877270-C-A

137540591-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24877270-C-G

137540591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24877270-C-T

137540613-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24877249-C-G

137540613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24877249-C-T

137540614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24877248-C-T

137540643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 24877208-G-T

137540646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24877205-A-G

137540682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24877169-T-C

137540691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24877160-A-G

137540791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 24877074-A-G

137540792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 24877073-G-A

137540792-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 24877073-G-T

http://identifiers.org/hco/9/GRCh38#137540806-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#24877062-A-C

137540806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 24877062-A-G

137540831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 24877037-G-A

137540831-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 24877037-G-C

137540831-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 24877037-G-T

137542574-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24873725-G-C

137542574-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24873725-G-T

http://identifiers.org/hco/9/GRCh38#137542609-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#24873693-C-A

137542609-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24873693-C-G

137542609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24873693-C-T

http://identifiers.org/hco/9/GRCh38#137542667-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#24873634-C-A

137542667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24873634-C-T

137542670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24873631-C-T

137542843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24873466-A-G

137542843-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24873466-A-T

137542880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24873452-G-A

137542880-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24873452-G-C

137542880-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24873452-G-T

137543044-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24873296-C-G

http://identifiers.org/hco/9/GRCh38#137543263-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#24872399-A-C

137543263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24872399-A-G

http://identifiers.org/hco/9/GRCh38#137543303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#24872329-C-A

137543303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24872329-C-T

137543510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24872104-A-G

http://identifiers.org/hco/9/GRCh38#137543607-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#24872013-C-A

137543607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24872013-C-T

http://identifiers.org/hco/9/GRCh38#137543611-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#24872009-C-A

137543611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24872009-C-T

137543677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24871928-C-T

http://identifiers.org/hco/9/GRCh38#137543689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#24871910-C-A

137543689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24871910-C-T

137543701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24871898-G-A

http://identifiers.org/hco/9/GRCh38#137543716-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#24871886-C-A

137543716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 24871886-C-T

http://identifiers.org/hco/9/GRCh38#137543848-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#24871754-C-A

137543874-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24871730-T-A

137543874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24871730-T-C

http://identifiers.org/hco/9/GRCh38#137543918-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#24871684-C-A

137543918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24871684-C-T

http://identifiers.org/hco/9/GRCh38#137543924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#24871678-C-A

137543924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24871678-C-T

137543938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24871664-G-A

137543938-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24871664-G-T

137546667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24870960-T-C

137546677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24870950-C-T

137546694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24870936-G-T

http://identifiers.org/hco/9/GRCh38#137546733-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#24870898-C-A

137546733-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24870898-C-G

137546733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24870898-C-T

http://identifiers.org/hco/9/GRCh38#137546981-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#24870591-C-A

http://identifiers.org/hco/9/GRCh38#137547186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#24870415-C-A

137547287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24870322-G-A

137547419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24870190-C-T

http://identifiers.org/hco/9/GRCh38#137547601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#24870102-C-A

137547601-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24870102-C-G

137547601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24870102-C-T

137548182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24868003-G-A

137548182-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24868003-G-C

137548215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24867958-G-A

137548220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24867956-C-T

137548667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24867495-G-A

137548730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24867442-A-G

137548733-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24867439-G-C

137549009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24867080-G-A

137549422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24866716-T-C

137549436-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24866702-G-C

137549438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24866700-T-C

137549562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24866588-T-C

http://identifiers.org/hco/9/GRCh38#137549567-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#24866583-C-A

137549567-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24866583-C-G

137549567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24866583-C-T

137549568-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24866582-T-A

137550016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24866465-G-T

137550018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24866463-G-A

137550018-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24866463-G-C

137550018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24866463-G-T

137550019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24866462-G-A

137550019-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24866462-G-T

http://identifiers.org/hco/9/GRCh38#137550045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#24866438-C-A

137550045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24866438-C-T

137550105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24866387-C-T

137550137-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24866363-A-T

http://identifiers.org/hco/9/GRCh38#137550248-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#24866245-A-C

137550286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, splice_region_variant, undefined
orthologous variants: 24866217-G-A

137550390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 24866116-G-A

137550390-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 24866116-G-C

137550390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24768
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 24866116-G-T