12775037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80828930-A-G

http://identifiers.org/hco/9/GRCh38#12775093-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#80828983-C-A

12775168-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80829091-G-T

12775245-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80829161-A-T

12775290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80829204-G-A

12775290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80829204-G-T

12775348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80829252-A-G

http://identifiers.org/hco/9/GRCh38#12775451-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#80829356-A-C

12775451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80829356-A-G

12775451-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80829356-A-T

http://identifiers.org/hco/9/GRCh38#12775505-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#80829408-A-C

12775505-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80829408-A-T

12775812-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80829688-C-G

12775812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80829688-C-T

12775813-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80829689-C-G

12775813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80829689-C-T

12775834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80829710-G-A

12775835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 80829711-G-A

12775835-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80829711-G-C

http://identifiers.org/hco/9/GRCh38#12775889-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#80829744-C-A

12775889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 80829744-C-T

12776148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80829966-G-A

12776148-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80829966-G-T

12776169-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80829987-T-A

12776423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 80830221-G-A

12776471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 80830269-G-A

12776593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80830363-G-A

12776593-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80830363-G-C

12776701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80830468-G-A

12776999-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80830767-C-G

http://identifiers.org/hco/9/GRCh38#12777098-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#80834955-A-C

12777098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80834955-A-G

12777099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80834956-G-A

12777257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80835006-A-G

12777328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80835095-G-A

12777328-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80835095-G-T

http://identifiers.org/hco/9/GRCh38#12777394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#80835149-C-A

12777394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80835149-C-T

12777507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80835253-G-A

12777507-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80835253-G-C

12777507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80835253-G-T

12777770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80836275-G-A

12777887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80836401-T-C

12789676-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80836926-C-G

12789676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80836926-C-T

12789906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80837158-G-A

12789957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80837205-T-C

12790135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80837379-G-T

12790180-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80837419-C-G

12790185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80837424-C-T

12790220-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80837456-T-G

12790397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80837617-T-C

http://identifiers.org/hco/9/GRCh38#12790433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#80837652-C-A

12790433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80837652-C-T

12790496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80837689-T-C

12790528-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80837716-G-T

12790639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80837812-G-A

12790639-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80837812-G-T

12790672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80837843-T-C

12790694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80837865-G-A

12790694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80837865-G-T

12790721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80837891-A-G

12790744-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80837913-A-T

12790913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80838076-T-C

12791032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80838175-C-T

12791145-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80838280-A-T

12791190-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80838325-G-C

12791218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80838353-T-C

12791418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80838557-G-A

http://identifiers.org/hco/9/GRCh38#12791582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#80838725-C-A

12791582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80838725-C-T

12791592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80838735-A-G

http://identifiers.org/hco/9/GRCh38#12791638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#80838773-C-A

12791658-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80838793-T-A

http://identifiers.org/hco/9/GRCh38#12791856-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#80838971-C-A

12791904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80839014-T-C

12792187-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80839126-G-T

12792677-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80839464-A-T

12792717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80839512-C-T

12792825-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80839649-G-C

12792864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80839707-A-G

12792880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80839723-G-A

12792912-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80839756-T-A

12793170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80840013-C-T

12793228-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80840064-T-A

12793238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80840074-T-C

12794293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 80840546-T-C

12794388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 80840664-T-C

12794422-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 80840699-C-G

12794579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80840837-C-T

12794665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80840920-T-C

12794786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80841037-C-T

12794792-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80841043-G-C

12794990-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80841237-C-G

12795181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80841410-G-A

12795232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80841460-G-A

12795235-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80841463-G-C

12795310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80841538-G-A

12795385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80841624-A-G

12795524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80841717-T-C

12795573-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80841765-T-A

12795717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80841907-A-G

12795731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80841921-G-A

12795848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80842026-C-T

http://identifiers.org/hco/9/GRCh38#12795951-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#80842120-A-C

12795958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80842127-A-G

12796298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80842358-T-C

http://identifiers.org/hco/9/GRCh38#12797305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#80843337-C-A

12797341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80843384-A-G

12797664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80843672-T-C

12797676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80843684-T-C

12797685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80843692-A-G

12797732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80843748-G-A

http://identifiers.org/hco/9/GRCh38#12797769-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#80843786-A-C

12798007-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80843985-G-C

12798035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80844012-G-A

12798090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80844061-T-C

12798168-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80844125-G-T

12798185-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80844142-G-C

12798229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80844183-A-G

12798232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80844186-T-C

12798239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80844193-G-A

12798288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80844246-T-C

12798459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80844408-G-A

http://identifiers.org/hco/9/GRCh38#12798499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#80844447-C-A

12798500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80844448-C-T

12798779-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80844727-C-G

http://identifiers.org/hco/9/GRCh38#12798846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#80844798-C-A

12798895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80844866-C-T

12799013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80844962-G-A

http://identifiers.org/hco/9/GRCh38#12799023-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#80844972-A-C

http://identifiers.org/hco/9/GRCh38#12799029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#80844978-C-A

12799224-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80845048-C-G

12799279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80845097-G-A

12799288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80845106-T-C

12799308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80845126-G-A

12801199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80850110-C-T

12801200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80850111-A-G

12801223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80850134-T-C

12801297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80850196-T-C

12801304-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80850203-T-A

12801306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80850205-T-C

12801728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80851137-T-C

12801759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80851170-G-T

12801879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80851303-A-G

12801942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80851379-A-G

12802753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80851774-C-T

12802754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80851775-G-A

12802802-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80851822-T-G

12802876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80851902-A-G

12803021-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80851998-T-G

12803158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80852115-A-G

12803385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80852515-T-C

http://identifiers.org/hco/9/GRCh38#12803584-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#80853262-A-C

12803755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80853420-G-A

12804641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80854715-T-C

12804673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80854747-T-C

12804673-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80854747-T-G

12804696-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80854779-A-T

12804714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80854797-T-C

12804715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80854798-G-A

12804829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80854918-G-A

12804904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80855012-G-A

12805341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80855565-G-A

12805341-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80855565-G-C

http://identifiers.org/hco/9/GRCh38#12805361-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#80855585-C-A

12805577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80855886-G-A

12805579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80855888-C-T

12805704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80855986-G-A

http://identifiers.org/hco/9/GRCh38#12805845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#80856109-C-A

http://identifiers.org/hco/9/GRCh38#12805912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#80856166-C-A

12805926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80856180-T-C

http://identifiers.org/hco/9/GRCh38#12806001-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#80856247-C-A

12806003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80856249-G-A

12806322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80856493-T-C

12806409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80856572-G-A

12806548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80856698-G-T

12806564-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80856707-T-G

http://identifiers.org/hco/9/GRCh38#12809834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#80857569-C-A

12809834-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80857569-C-G

12809906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80857640-T-C

http://identifiers.org/hco/9/GRCh38#12810011-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#80857713-C-A

12810011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80857713-C-T

12810086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80857799-C-T

12810121-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80857834-G-C

12810127-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80857843-A-T

12810129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80857845-G-T

12810255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80857925-C-T

12810261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80857931-A-G

12810310-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80857980-C-G

12810310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80857980-C-T

http://identifiers.org/hco/9/GRCh38#12810519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#80858168-C-A

12810594-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80858236-A-T

12810595-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80858237-T-G

12810691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80858329-A-G

http://identifiers.org/hco/9/GRCh38#12810709-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#80858347-A-C

12810743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80858381-G-A

12811023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80858665-C-T

12811127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80858765-T-C

12811182-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80858815-T-G

12811298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80858930-A-G

12811298-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80858930-A-T

12811457-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80859069-T-G

12811677-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80859240-T-A

12811687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80859249-C-T

12811934-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80859494-G-C

http://identifiers.org/hco/9/GRCh38#12812030-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#80859574-C-A

12812102-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80859618-A-T

12812419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80860575-G-A

12812419-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80860575-G-C

12812450-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80860606-C-G

12812571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80860730-A-G

12812869-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80861305-G-T

12813107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80862104-A-G

12813305-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80862277-T-G

12813309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80862281-T-C

12814136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80865137-G-A

12814162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80865163-T-C

12814165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80865166-G-A

12814200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80865193-A-G

12814416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron variant
orthologous variants: 80865400-G-A

12814697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron variant
orthologous variants: 80865429-C-T

http://identifiers.org/hco/9/GRCh38#12814704-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#80865436-A-C

http://identifiers.org/hco/9/GRCh38#12814749-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#80865477-A-C

12814750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron variant
orthologous variants: 80865478-T-C

12814790-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron variant
orthologous variants: 80865517-T-A

http://identifiers.org/hco/9/GRCh38#12814793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#80865520-C-A

http://identifiers.org/hco/9/GRCh38#12814879-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#80865594-A-C

12814997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron variant
orthologous variants: 80865679-T-C

12815016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron variant
orthologous variants: 80865698-C-T

12815060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron variant
orthologous variants: 80865741-A-G

12815066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron variant
orthologous variants: 80865747-T-C

12815108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron variant
orthologous variants: 80865789-T-C

http://identifiers.org/hco/9/GRCh38#12816262-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#80866958-A-C

12816287-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron variant
orthologous variants: 80866980-T-A

http://identifiers.org/hco/9/GRCh38#12816477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#80867156-C-A

12816751-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron variant
orthologous variants: 80867841-T-G

12816855-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron variant
orthologous variants: 80867949-A-T

12817479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron variant
orthologous variants: 80868508-A-G

http://identifiers.org/hco/9/GRCh38#12817480-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#80868509-C-A

12817496-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron variant
orthologous variants: 80868525-T-A

12817602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron variant
orthologous variants: 80868627-C-T

12817629-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron variant
orthologous variants: 80868655-C-G

12817879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron variant
orthologous variants: 80868887-G-A

12817921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron variant
orthologous variants: 80868904-G-A

12817960-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron variant
orthologous variants: 80868946-C-G

12818090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron variant
orthologous variants: 80869060-C-T

12818254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron variant
orthologous variants: 80869215-A-G

12818325-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron variant
orthologous variants: 80869265-C-G

12818502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron variant
orthologous variants: 80869682-T-C

12818687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron variant
orthologous variants: 80869882-T-C

12818795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron variant
orthologous variants: 80869973-A-G

12818806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron variant
orthologous variants: 80869984-C-T

12818864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron variant
orthologous variants: 80870041-T-C

12818900-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron variant
orthologous variants: 80870077-G-C

12818947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron variant
orthologous variants: 80870116-G-A

12819127-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron variant
orthologous variants: 80870303-G-C

12819130-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron variant
orthologous variants: 80870306-G-C

12819296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron variant
orthologous variants: 80870609-T-C

12819365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron variant
orthologous variants: 80870696-G-A

http://identifiers.org/hco/9/GRCh38#12819632-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#80871065-C-A

12820735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron variant
orthologous variants: 80871151-A-G

12820867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron variant
orthologous variants: 80871281-G-A

12820917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron variant
orthologous variants: 80871338-G-A

12820917-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron variant
orthologous variants: 80871338-G-C

12820943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron variant
orthologous variants: 80871359-T-C

12820949-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron variant
orthologous variants: 80871365-G-T

12821024-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron variant
orthologous variants: 80871427-C-G

http://identifiers.org/hco/9/GRCh38#12821042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#80871430-C-A

12821042-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron variant
orthologous variants: 80871430-C-G

12821042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron variant
orthologous variants: 80871430-C-T

12821048-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron variant
orthologous variants: 80871436-C-G

12821125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron variant
orthologous variants: 80871507-G-A

12821125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron variant
orthologous variants: 80871507-G-T

12821158-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron variant
orthologous variants: 80871540-T-G

http://identifiers.org/hco/9/GRCh38#12821265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#80871651-C-A

12821265-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron variant
orthologous variants: 80871651-C-G

http://identifiers.org/hco/9/GRCh38#12821305-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#80871722-A-C

12821305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron variant
orthologous variants: 80871722-A-G

12821309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron variant
orthologous variants: 80871725-G-A

12821309-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron variant
orthologous variants: 80871725-G-C

12821309-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron variant
orthologous variants: 80871725-G-T

12821380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 80871791-C-T

12821641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: missense variant
orthologous variants: 80872055-G-A

12821641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: missense variant
orthologous variants: 80872055-G-T

12821724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: synonymous variant
orthologous variants: 80872138-T-C

12821724-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: synonymous variant
orthologous variants: 80872138-T-G

12821804-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: 3 prime UTR variant
orthologous variants: 80872221-T-A

12821866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: 3 prime UTR variant
orthologous variants: 80872280-A-G

12821899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: 3 prime UTR variant
orthologous variants: 80872313-T-C

12821972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: 3 prime UTR variant
orthologous variants: 80872385-A-G

12821972-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: 3 prime UTR variant
orthologous variants: 80872385-A-T

http://identifiers.org/hco/9/GRCh38#12821986-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#80872400-C-A

12821995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: 3 prime UTR variant
orthologous variants: 80872409-A-G

12822135-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: 3 prime UTR variant
orthologous variants: 80872547-T-A

12822135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: 3 prime UTR variant
orthologous variants: 80872547-T-C

12822135-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: 3 prime UTR variant
orthologous variants: 80872547-T-G

12822154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: 3 prime UTR variant
orthologous variants: 80872566-T-C

12822204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: 3 prime UTR variant
orthologous variants: 80872617-A-G

12822205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: 3 prime UTR variant
orthologous variants: 80872618-T-C

12822209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: 3 prime UTR variant
orthologous variants: 80872622-A-G

12822248-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: 3 prime UTR variant
orthologous variants: 80872660-T-G

http://identifiers.org/hco/9/GRCh38#12822258-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#80872670-A-C

12822468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: 3 prime UTR variant
orthologous variants: 80872877-G-A

http://identifiers.org/hco/9/GRCh38#12822495-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#80872904-C-A

12822791-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: 3 prime UTR variant
orthologous variants: 80873623-T-A

12822871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: 3 prime UTR variant
orthologous variants: 80873692-T-C

12822910-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: 3 prime UTR variant
orthologous variants: 80873730-T-A

12822927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: 3 prime UTR variant
orthologous variants: 80873764-T-C

12822943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: 3 prime UTR variant
orthologous variants: 80873774-G-A

http://identifiers.org/hco/9/GRCh38#12823057-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31452
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#80873876-C-A