222567057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 78400051-A-G

222567126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 78400110-G-A

http://identifiers.org/hco/2/GRCh38#222567130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#78400114-C-A

http://identifiers.org/hco/2/GRCh38#222567161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#78400145-C-A

222567161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 78400145-C-T

222567244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 78400215-A-G

222567250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 78400221-T-C

222567270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 78400242-C-T

222567558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 78400504-G-T

222571342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 78401433-A-G

222571479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 78401533-A-G

http://identifiers.org/hco/2/GRCh38#222571688-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#78401684-A-C

222571688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 78401684-A-G

222571688-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 78401684-A-T

http://identifiers.org/hco/2/GRCh38#222571816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#78401796-C-A

222571932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 78401892-G-A

222571932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 78401892-G-T

http://identifiers.org/hco/2/GRCh38#222571979-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#78401939-C-A

222572016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 78401976-G-A

222572016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 78401976-G-T

222572130-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78402093-A-T

http://identifiers.org/hco/2/GRCh38#222572155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#78402115-C-A

222572155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78402115-C-T

http://identifiers.org/hco/2/GRCh38#222572368-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#78402227-A-C

222572465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78402316-A-G

222572470-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78402321-G-C

222572649-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78402488-T-A

222572694-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78402538-T-A

222573150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78403005-G-A

222573192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78403043-A-G

222573219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78403069-T-C

222573269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78403110-C-T

222574052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78403823-T-C

222574052-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78403823-T-G

222574181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78403943-A-G

222574949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78404533-A-G

http://identifiers.org/hco/2/GRCh38#222574951-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#78404535-C-A

222574951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78404535-C-T

222575049-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78404617-G-C

http://identifiers.org/hco/2/GRCh38#222575082-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#78404633-A-C

222575529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78405504-A-G

222575533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78405508-T-C

http://identifiers.org/hco/2/GRCh38#222575689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#78405662-C-A

222575689-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78405662-C-G

222575851-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78405766-T-A

222576018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78405921-T-C

222576117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78406020-C-T

222576391-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78406302-G-T

222576654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78406531-C-T

222577459-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78407145-A-T

222577484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78407159-G-A

http://identifiers.org/hco/2/GRCh38#222577570-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#78407187-A-C

222577877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78407494-G-A

222578092-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78407686-T-G

222578139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78407722-T-C

http://identifiers.org/hco/2/GRCh38#222578141-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#78407724-A-C

222579155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78408328-T-C

222579244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78408417-C-T

222579440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78408770-A-G

222579472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78408838-C-T

222579650-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78409001-G-C

222581501-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78409973-T-A

222594635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78415979-G-A

222594771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78416091-C-T

222595087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78416358-T-C

http://identifiers.org/hco/2/GRCh38#222595186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#78416422-C-A

222595392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78416614-G-A

http://identifiers.org/hco/2/GRCh38#222595717-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#78416948-C-A

222595988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78417209-T-C

222596014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78417235-C-T

222596262-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78417482-C-G

222596262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78417482-C-T

222596350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78417571-G-A

222596560-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78417754-T-A

http://identifiers.org/hco/2/GRCh38#222596641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#78417828-C-A

222596791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78417890-G-A

222596794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78417893-T-C

222596796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78417895-C-T

222596839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78417942-T-C

222597062-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78418104-C-G

222597126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78418167-G-T

http://identifiers.org/hco/2/GRCh38#222597458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#78418544-C-A

222597655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78418729-C-T

222598720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78419182-G-A

222599015-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78419460-T-A

222599030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78419475-A-G

222599170-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78419629-G-T

222599322-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78419781-G-C

222599607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78419981-C-T

222599822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78420165-C-T

222599826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78420179-T-C

http://identifiers.org/hco/2/GRCh38#222599853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#78420212-C-A

222599888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78420246-G-A

222599888-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78420246-G-T

222600038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 78420382-T-C

222600257-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78420578-C-G

222600401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78420710-T-C

http://identifiers.org/hco/2/GRCh38#222600403-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#78420712-C-A

222600883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78421194-T-C

222600888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78421199-T-C

222603158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78422678-G-A

222603264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78422789-G-A

222603316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78422836-T-C

222603316-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78422836-T-G

222603647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78423048-T-C

222603922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78423219-T-C

222604254-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78423236-T-A

222604254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78423236-T-C

http://identifiers.org/hco/2/GRCh38#222604359-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#78423340-C-A

http://identifiers.org/hco/2/GRCh38#222605167-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#78423821-C-A

222605206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78423860-T-C

222605384-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78424033-T-A

222605384-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78424033-T-G

http://identifiers.org/hco/2/GRCh38#222605717-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#78424287-A-C

222608681-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78427440-T-A

222608732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78427489-G-A

222608732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78427489-G-T

222609742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78428398-G-A

222610474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78429552-T-C

222610483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78429561-T-C

222610498-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78429566-A-T

http://identifiers.org/hco/2/GRCh38#222610540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#78429598-C-A

222610911-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78429930-C-G

222611023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78430045-C-T

222611301-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78430304-T-A

222612648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78430748-A-G

http://identifiers.org/hco/2/GRCh38#222612729-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#78430814-C-A

222612866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78430930-C-T

222613668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78431291-T-C

222613768-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78431354-T-G

222613817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 78431397-T-C

222613835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 78431415-T-C

222613955-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78431535-T-A

222613955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78431535-T-C

222613955-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78431535-T-G

222616086-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78433276-G-C

222616568-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78433493-T-A

222616568-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78433493-T-G

222618292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78434178-C-T

222618356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78434246-C-T

http://identifiers.org/hco/2/GRCh38#222618605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#78434420-C-A

222618654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78434466-C-T

222618930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78434679-C-T

222619014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78434752-C-T

222619394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78431935-G-A

222619500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78435077-A-G

222619500-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78435077-A-T

http://identifiers.org/hco/2/GRCh38#222619592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#78435164-C-A

222619654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 78435211-A-G

222619678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 78435235-G-A

222619678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 78435235-G-T

222619808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78435362-G-A

222619852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78435389-G-A

222619852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78435389-G-T

222619885-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78435422-T-G

http://identifiers.org/hco/2/GRCh38#222620154-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#78435662-C-A

222620292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78435801-T-C

222620882-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78436296-G-T

http://identifiers.org/hco/2/GRCh38#222621021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#78436520-C-A

222621021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78436520-C-T

222621142-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78436637-A-T

222621640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78437050-A-G

222621684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78437091-T-C

222621736-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78437121-T-A

222621972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78437521-G-A

222621972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78437521-G-T

222622369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78437813-G-A

http://identifiers.org/hco/2/GRCh38#222622385-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#78437828-C-A

222622439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78437882-A-G

222622741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78438122-G-A

http://identifiers.org/hco/2/GRCh38#222622755-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#78438136-C-A

222623624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78438918-G-A

222623624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78438918-G-T

222623757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78439051-T-C

222623806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78439092-G-T

http://identifiers.org/hco/2/GRCh38#222623904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#78439158-C-A

222623904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78439158-C-T

222623987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78439184-A-G

222624089-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78439288-G-C

222624160-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78439360-G-T

222624222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78439423-A-G

222624381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 78439581-G-T

222624500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78439699-C-T

http://identifiers.org/hco/2/GRCh38#222624578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#78439777-C-A

222624857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78440050-T-C

222624886-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78440079-A-G

222625259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78440604-T-C

222627925-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78443011-G-C

222628510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78443408-T-C

222628587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78443476-C-T

222628932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78443706-G-A

222628932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78443706-G-T

http://identifiers.org/hco/2/GRCh38#222628997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#78443767-C-A

222629310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78444101-T-C

222629449-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78444171-T-A

222629593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78444279-G-A

222629669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78444341-G-A

222630141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 78444636-A-G

http://identifiers.org/hco/2/GRCh38#222630226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#78444723-C-A

222630226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78444723-C-T

222630257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78444750-A-G

222631086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78445656-A-G

222631515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78445801-A-G

http://identifiers.org/hco/2/GRCh38#222631546-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#78445830-C-A

http://identifiers.org/hco/2/GRCh38#222631604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#78445889-C-A

222631604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 78445889-C-T

http://identifiers.org/hco/2/GRCh38#222631754-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#78446024-A-C

222632443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78446729-A-G

222632619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78446897-G-T

222633230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 78447751-A-G

http://identifiers.org/hco/2/GRCh38#222633371-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#78447889-A-C

222633371-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78447889-A-T

222633386-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78447904-T-A

222633387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78447905-A-G

222633387-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78447905-A-T

222633882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78448105-C-T

222634381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78449111-G-A

222634381-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78449111-G-C

222634381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78449111-G-T

http://identifiers.org/hco/2/GRCh38#222634383-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#78449113-A-C

222634383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 78449113-A-G

222634472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 78449202-T-C

222634472-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 78449202-T-G

http://identifiers.org/hco/2/GRCh38#222634622-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#78449326-A-C

222634691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78449388-G-T

222638597-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78450313-T-G

222639546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78452792-G-A

222639546-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78452792-G-C

222639546-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78452792-G-T

http://identifiers.org/hco/2/GRCh38#222639557-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#78452803-A-C

222639557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78452803-A-G

222639585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 78452832-A-G

222639806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78453056-C-T

222640784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78454752-T-C

http://identifiers.org/hco/2/GRCh38#222640807-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#78454775-C-A

222640807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78454775-C-T

222640818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78454786-A-G

http://identifiers.org/hco/2/GRCh38#222640819-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#78454787-A-C

222640819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78454787-A-G

222640822-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78454792-G-T

222640833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78454803-A-G

222640839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78454809-A-G

222640854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 78454822-C-T

222640876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 78454844-T-C

222640910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 78454878-T-C

222640919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 78454887-T-C

222640993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78454955-A-G

222640993-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78454955-A-T

222641389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78455358-G-A

222641532-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78455477-A-T

222641934-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78455832-T-A

222642391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78456186-C-T

222642444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78456236-G-A

222642444-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78456236-G-T

222642556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78456345-C-T

222642557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78456346-G-A

http://identifiers.org/hco/2/GRCh38#222642708-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#78456462-C-A

222642732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78456482-G-T

222642735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78456486-A-G

222642778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78456530-T-C

222642823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78456575-A-G

http://identifiers.org/hco/2/GRCh38#222643016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#78456758-C-A

222643016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78456758-C-T

222643156-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78456812-T-A

222643156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78456812-T-C

222643168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78456826-G-A

222643177-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78456835-T-A

222643575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78457150-C-T

222643713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78457266-A-G

222644306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78457943-A-G

222644462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78458060-T-C

222644482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78458080-A-G

222648663-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78458480-G-T

222648923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78459122-T-C

http://identifiers.org/hco/2/GRCh38#222649231-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#78459384-A-C

222649426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78459578-C-T

222650002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78460185-C-T

222650033-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78460216-T-A

222650034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78460217-G-A

222650141-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78460305-G-C

222650747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78461057-G-T

222650772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78461082-C-T

222650973-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78461243-C-G

222651148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78461424-T-C

222651359-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78461621-C-G

222651534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78461773-C-T

222651559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78461798-T-C

222651745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78461995-T-C

222651875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78462122-G-A

222652452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78462589-G-A

222652474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78462611-T-C

222653043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78463320-T-C

222653192-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78463481-T-G

222653208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78463497-C-T

222653424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78463675-G-A

222653434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78463677-A-G

222653446-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78463689-T-A

222653446-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78463689-T-G

222654611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78464222-T-C

222655273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78464651-T-C

222655397-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78464777-T-A

222655397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78464777-T-C

222655403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78464782-G-A

222655416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78464797-T-C

222655772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78465178-G-A

222655940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78465350-G-A

222655940-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78465350-G-C

222655940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78465350-G-T

222655969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78465379-G-A

222655969-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78465379-G-C

222655969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78465379-G-T

222655998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78465404-T-C

http://identifiers.org/hco/2/GRCh38#222656006-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#78465412-C-A

222656006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17800
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78465412-C-T