73207503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 113552301-G-A

73207503-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 113552301-G-T

73207504-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 113552302-G-C

73207504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 113552302-G-T

73207505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 113552303-G-A

73207505-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 113552303-G-C

73207515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 113552313-G-T

73207627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 113552414-G-A

73207665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 113552445-G-A

73207665-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 113552445-G-C

73207666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 113552446-T-C

73207668-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 113552448-T-A

73207705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, undefined
orthologous variants: 113552485-G-A

73207705-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, undefined
orthologous variants: 113552485-G-C

73207705-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, undefined
orthologous variants: 113552485-G-T

73207712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, undefined
orthologous variants: 113552492-A-G

73207744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 113552524-T-C

73207744-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 113552524-T-G

73207835-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 113552597-T-G

73207848-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 113552610-T-A

73207853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 113552615-T-C

73207907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 113552670-G-A

73207907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 113552670-G-T

73207919-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 113552682-T-G

73208016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 113552756-T-C

73208054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 113552791-G-A

73208054-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 113552791-G-T

73208074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 113552809-G-A

73208074-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 113552809-G-C

73208074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 113552809-G-T

73208081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 113552816-C-T

http://identifiers.org/hco/17/GRCh38#73208099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#113552834-C-A

73208117-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 113552850-G-T

http://identifiers.org/hco/17/GRCh38#73208138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#113552871-C-A

73208138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 113552871-C-T

73208194-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 113552914-T-G

73208215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 113552935-G-A

73208215-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 113552935-G-C

73208215-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 113552935-G-T

73208226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 113552946-G-A

http://identifiers.org/hco/17/GRCh38#73208301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#113553019-C-A

73208301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 113553019-C-T

73208318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3_prime_UTR_variant, missense_variant, undefined
orthologous variants: 113553037-T-C

73208325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3_prime_UTR_variant, synonymous_variant, undefined
orthologous variants: 113553044-G-A

http://identifiers.org/hco/17/GRCh38#73208351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3_prime_UTR_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#113553070-C-A

73208351-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3_prime_UTR_variant, missense_variant, undefined
orthologous variants: 113553070-C-G

73208370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3_prime_UTR_variant, synonymous_variant, undefined
orthologous variants: 113553092-C-T

http://identifiers.org/hco/17/GRCh38#73208394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3_prime_UTR_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#113553116-C-A

73208394-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3_prime_UTR_variant, missense_variant, undefined
orthologous variants: 113553116-C-G

73208394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3_prime_UTR_variant, synonymous_variant, undefined
orthologous variants: 113553116-C-T

73208523-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3 prime UTR variant
orthologous variants: 113553243-C-G

73208523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3 prime UTR variant
orthologous variants: 113553243-C-T

73208532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3 prime UTR variant
orthologous variants: 113553252-A-G

73208576-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3 prime UTR variant
orthologous variants: 113553295-T-A

73208576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3 prime UTR variant
orthologous variants: 113553295-T-C

73208646-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3 prime UTR variant
orthologous variants: 113553313-T-G

73208655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3 prime UTR variant
orthologous variants: 113553322-A-G

73208696-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3 prime UTR variant
orthologous variants: 113553361-T-A

http://identifiers.org/hco/17/GRCh38#73208742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#113553395-C-A

73208750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3 prime UTR variant
orthologous variants: 113553403-T-C

73208750-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3 prime UTR variant
orthologous variants: 113553403-T-G

73208751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3 prime UTR variant
orthologous variants: 113553404-G-A

73208751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3 prime UTR variant
orthologous variants: 113553404-G-T

73208805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3 prime UTR variant
orthologous variants: 113553450-G-A

73208821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3 prime UTR variant
orthologous variants: 113553465-A-G

73208821-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3 prime UTR variant
orthologous variants: 113553465-A-T

73208835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3 prime UTR variant
orthologous variants: 113553479-G-T

http://identifiers.org/hco/17/GRCh38#73208906-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#113553524-A-C

73208906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3 prime UTR variant
orthologous variants: 113553524-A-G

73208906-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3 prime UTR variant
orthologous variants: 113553524-A-T

http://identifiers.org/hco/17/GRCh38#73208931-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#113553542-C-A

73208931-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3 prime UTR variant
orthologous variants: 113553542-C-G

73208931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3 prime UTR variant
orthologous variants: 113553542-C-T

http://identifiers.org/hco/17/GRCh38#73208933-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#113553544-A-C

73208933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3 prime UTR variant
orthologous variants: 113553544-A-G

73208954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3 prime UTR variant
orthologous variants: 113553570-C-T

73208963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3 prime UTR variant
orthologous variants: 113553579-T-C

73208979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3 prime UTR variant
orthologous variants: 113553589-G-T

73209038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3 prime UTR variant
orthologous variants: 113553647-T-C

73209040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3 prime UTR variant
orthologous variants: 113553649-T-C

73209151-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3 prime UTR variant
orthologous variants: 113553764-T-A

73209151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3 prime UTR variant
orthologous variants: 113553764-T-C

73209151-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3 prime UTR variant
orthologous variants: 113553764-T-G

http://identifiers.org/hco/17/GRCh38#73209159-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#113553772-C-A

73209213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3 prime UTR variant
orthologous variants: 113553826-G-A

73209213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3 prime UTR variant
orthologous variants: 113553826-G-T

73209220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3 prime UTR variant
orthologous variants: 113553833-A-G

73209225-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3 prime UTR variant
orthologous variants: 113553838-G-C

73209225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3 prime UTR variant
orthologous variants: 113553838-G-T

http://identifiers.org/hco/17/GRCh38#73209274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#113553855-C-A

http://identifiers.org/hco/17/GRCh38#73209298-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#113553879-C-A

73209298-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3 prime UTR variant
orthologous variants: 113553879-C-G

73209330-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3 prime UTR variant
orthologous variants: 113553924-T-A

73209340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3 prime UTR variant
orthologous variants: 113553934-C-T

http://identifiers.org/hco/17/GRCh38#73209362-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#113553956-C-A

http://identifiers.org/hco/17/GRCh38#73209367-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#113553961-C-A

http://identifiers.org/hco/17/GRCh38#73209370-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#113553964-C-A

73209414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3 prime UTR variant
orthologous variants: 113554011-G-A

73209468-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3 prime UTR variant
orthologous variants: 113554072-G-T

73209481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3 prime UTR variant
orthologous variants: 113554085-A-G

73209523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 113554127-G-A

73209523-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 113554127-G-T

http://identifiers.org/hco/17/GRCh38#73209574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#113554181-C-A

73209574-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 113554181-C-G

73209631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 113554238-G-A

73209631-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 113554238-G-C

73209631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 113554238-G-T

73209637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 113554244-G-A

73209637-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 113554244-G-C

73209637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 113554244-G-T

73209664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 113554271-G-A

73209664-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 113554271-G-C

73209664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 113554271-G-T

73209667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 113554274-C-T

73212032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113555540-A-G

http://identifiers.org/hco/17/GRCh38#73212122-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#113555622-C-A

73212419-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113555852-T-G

73212586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113555978-C-T

73212651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113556041-G-A

73212651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113556041-G-T

73212652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113556042-G-A

73212652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113556042-G-T

73212659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113556049-C-T

73212667-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113556057-T-G

http://identifiers.org/hco/17/GRCh38#73212824-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#113556207-C-A

73213979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113557383-A-G

73214094-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113557504-C-G

73215709-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113558150-A-T

73215730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113558171-A-G

73215803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113558246-G-A

73215925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113558358-T-C

73216190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113558626-G-A

73216244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113558671-G-A

73216535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113558930-G-A

http://identifiers.org/hco/17/GRCh38#73216548-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#113558944-A-C

73216876-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113559208-T-G

73216880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113559212-C-T

73218097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113561121-A-G

73221490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113563642-T-C

73221706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113563843-T-C

73221706-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113563843-T-G

73221935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113564086-G-A

http://identifiers.org/hco/17/GRCh38#73222027-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#113564158-C-A

73222027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113564158-C-T

http://identifiers.org/hco/17/GRCh38#73222064-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#113564195-A-C

http://identifiers.org/hco/17/GRCh38#73222102-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#113564236-C-A

73222978-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113564786-T-A

73222978-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113564786-T-G

73225135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113565733-C-T

73225167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113565764-G-A

http://identifiers.org/hco/17/GRCh38#73227141-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#113568102-A-C

73227141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113568102-A-G

73227610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113568482-T-C

73227756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113568655-A-G

http://identifiers.org/hco/17/GRCh38#73227854-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#113568751-A-C

73227854-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 113568751-A-T

http://identifiers.org/hco/17/GRCh38#73227876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#113568773-C-A

73227876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113568773-C-T

http://identifiers.org/hco/17/GRCh38#73227886-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#113568782-C-A

73227886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113568782-C-T

73227926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113568816-T-C

73228057-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 113568962-T-A

73230987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113573062-C-T

73231037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113573112-G-A

73231054-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113573277-C-G

73231216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113573437-A-G

73231216-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113573437-A-T

73231603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113574173-A-G

http://identifiers.org/hco/17/GRCh38#73231739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#113574333-C-A

73231789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113574380-G-A

73232000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113574599-G-T

73232412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113575016-G-A

73232412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113575016-G-T

http://identifiers.org/hco/17/GRCh38#73232448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#113575045-C-A

73232448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 113575045-C-T

http://identifiers.org/hco/17/GRCh38#73232484-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#113575081-C-A

73232484-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 113575081-C-G

73232484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 113575081-C-T

73232487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 113575084-A-G

73232495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 113575092-G-A

73232495-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 113575092-G-T

http://identifiers.org/hco/17/GRCh38#73232543-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#113575140-A-C

73232543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 113575140-A-G

73232668-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 113575271-T-G

73232694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113575291-G-A

73232694-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113575291-G-C

73232694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113575291-G-T

73232707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113575304-G-A

73232707-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113575304-G-C

73232707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113575304-G-T

73232734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113575332-G-T

73232771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113575368-C-T

73232786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113575383-G-A

73232786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113575383-G-T

73232801-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113575391-G-C

73232801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113575391-G-T

73232803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113575393-G-A

73232803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113575393-G-T

73233163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113575813-C-T

73233173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113575826-T-C

73233226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113575862-A-G

http://identifiers.org/hco/17/GRCh38#73233359-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#113575981-C-A

73233359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113575981-C-T

73233388-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113576005-G-C

73233388-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113576005-G-T

73233579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113576149-G-A

http://identifiers.org/hco/17/GRCh38#73233591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#113576157-C-A

73233597-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113576163-C-G

73233600-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113576166-A-T

73233601-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113576167-C-G

73233601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113576167-C-T

73233685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113576270-G-A

73233693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113576278-G-A

73233697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113576282-C-T

http://identifiers.org/hco/17/GRCh38#73233928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#113576390-C-A

73234071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113576546-C-T

73234081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113576556-A-G

http://identifiers.org/hco/17/GRCh38#73234195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#113576781-C-A

73234195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113576781-C-T

73235448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113578572-C-T

73235501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 113578625-A-G

73235574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 113578698-T-C

73235586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 113578710-T-C

73235602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 113578726-A-G

73235725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 113578843-G-A

73235725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 113578843-G-T

73235854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 113578972-A-G

73236005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 113579120-G-A

73236005-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 113579120-G-C

73236209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 113579321-A-G

73236230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 113579345-A-G

http://identifiers.org/hco/17/GRCh38#73236249-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#113579364-A-C

73236249-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 113579364-A-T

73236354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 113579463-A-G

73236393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 113579496-T-C

73236458-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 113579561-A-T

73236459-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 113579562-C-G

http://identifiers.org/hco/17/GRCh38#73236532-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#113579618-A-C

73236532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 113579618-A-G

73236562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 113579638-G-A

73236634-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 113579695-T-G

73236680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113579741-G-A

73236696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113579757-A-G

73236696-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113579757-A-T

73236721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25918
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 113579776-G-A