158769144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 5 prime UTR variant
orthologous variants: 79474978-G-A

158769144-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 5 prime UTR variant
orthologous variants: 79474978-G-C

158769144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 5 prime UTR variant
orthologous variants: 79474978-G-T

http://identifiers.org/hco/4/GRCh38#158769162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#79474963-C-A

158769162-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 79474963-C-G

158769162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 79474963-C-T

158769172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 79474953-G-A

158769172-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 79474953-G-C

158769172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 79474953-G-T

http://identifiers.org/hco/4/GRCh38#158769192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#79474929-C-A

158769192-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 79474929-C-G

158769192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 79474929-C-T

http://identifiers.org/hco/4/GRCh38#158769225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79474896-C-A

http://identifiers.org/hco/4/GRCh38#158769228-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79474893-C-A

158769228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 79474893-C-T

158769229-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 79474892-T-A

158769229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 79474892-T-C

158769343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79474787-T-C

158769428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79474674-G-A

158769428-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79474674-G-T

158769533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79474534-C-T

158770142-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79473966-T-G

158770206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79473910-C-T

158770381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79473695-T-C

158770415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79473664-C-T

158770439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79473612-T-C

158770593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79473260-G-T

158772791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79470474-C-T

158773087-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79470098-G-C

158773418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79469280-T-C

158773487-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79469203-C-G

158773717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79468967-C-T

158774515-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79467891-C-G

158774517-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79467886-T-G

158774526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79467877-A-G

158775023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79467011-A-G

http://identifiers.org/hco/4/GRCh38#158775148-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79466875-A-C

158775148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79466875-A-G

158775153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79466870-C-T

158775277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79466769-G-A

158775279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79466767-G-A

http://identifiers.org/hco/4/GRCh38#158776137-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79464094-C-A

158776263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79463985-T-C

158776961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79463142-C-T

158777039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79463068-C-T

http://identifiers.org/hco/4/GRCh38#158777404-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79462743-C-A

158779152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79461054-T-C

158779421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79460546-A-G

158782914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79460259-A-G

158783956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79458252-G-A

158783959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79458249-G-A

158784246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79457954-T-C

158784337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79457870-G-A

158788804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79456513-G-A

158788959-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79456353-C-G

158788959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79456353-C-T

158789007-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79456307-C-G

158789119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79456202-T-C

158789180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79456149-G-T

158791706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79452300-A-G

158791882-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79452207-G-T

158791885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79452204-G-A

158791943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79452159-G-A

158793757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79451498-C-T

158793774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79451481-A-G

158793815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79451443-G-A

158793868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79451389-C-T

158796028-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79450901-T-A

158796028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79450901-T-C

http://identifiers.org/hco/4/GRCh38#158796032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79450894-C-A

158796040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79450877-A-G

158796358-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79450589-T-G

158796475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79450476-A-G

http://identifiers.org/hco/4/GRCh38#158796690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79450293-C-A

158796733-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79450250-T-A

158799320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79446977-A-G

158799327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79446970-T-C

158799503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79446717-A-G

158799606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79446611-A-G

http://identifiers.org/hco/4/GRCh38#158800128-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79445755-C-A

158801879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79444370-A-G

158801965-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79444302-G-C

158802047-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79443524-A-T

158802630-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79443065-G-C

158802691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79443005-A-G

158802791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79442904-G-T

158802966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79442741-A-G

158803053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79442602-G-A

158803190-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79442499-C-G

158803190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79442499-C-T

http://identifiers.org/hco/4/GRCh38#158803247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79442447-C-A

158803360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79442175-T-C

158803361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79442174-G-A

158803553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79442010-T-C

158803711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79441862-C-T

http://identifiers.org/hco/4/GRCh38#158803724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79441849-C-A

158803724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79441849-C-T

158803900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79441716-C-T

158805053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79440066-T-C

158805119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79440040-C-T

158805426-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79439812-G-T

158805554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79439663-A-G

158805832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79439393-A-G

158806233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79439038-T-C

158806318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 79438953-A-G

158806415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 79438856-C-T

http://identifiers.org/hco/4/GRCh38#158806709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79438570-C-A

http://identifiers.org/hco/4/GRCh38#158807833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79438020-C-A

158807833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79438020-C-T

158808281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79437655-G-A

158808528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79436790-C-T

158808530-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79436788-C-G

158808534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79436784-T-C

158808584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 79436731-T-C

http://identifiers.org/hco/4/GRCh38#158808727-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79436596-A-C

158808743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79436580-T-C

http://identifiers.org/hco/4/GRCh38#158808791-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79436538-C-A

158808796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79436533-A-G

158809500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79436282-A-G

158810119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79435681-G-A

158810169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79435636-G-A

158810414-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79435395-T-G

158810485-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79435328-G-C

http://identifiers.org/hco/4/GRCh38#158810631-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79435197-A-C

158810937-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79434982-T-G

158811041-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79434880-G-C

158818242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79432468-C-T

158819795-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79431433-A-T

158819806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79431422-G-A

158819824-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79431404-C-G

158819970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79431257-A-G

158820069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79431149-A-G

158820419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79430701-T-C

158820572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79430378-C-T

158820704-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79430266-C-G

158820715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79430250-G-A

158820898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79430078-A-G

158823872-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79427332-C-G

158823960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79427259-A-G

158823982-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79427240-G-C

158824232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79426998-G-A

158824232-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79426998-G-C

158824304-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79426917-G-C

158824377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79426840-G-A

158824724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79426564-G-T

158825053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79426139-C-T

158825221-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79426006-T-A

158825324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79425910-G-A

158825362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79425890-G-A

158825379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79425874-C-T

158825623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79425693-G-A

http://identifiers.org/hco/4/GRCh38#158825775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79425592-C-A

158826013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 79425399-G-A

158826013-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 79425399-G-C

158826062-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79425350-T-A

158826167-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79425303-G-T

http://identifiers.org/hco/4/GRCh38#158826182-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79425290-A-C

158826218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79425271-C-T

158826244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79425253-A-G

158826405-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79425108-A-T

158826408-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79425105-G-C

158826425-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79425083-A-T

158826556-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79424868-C-G

158826594-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79424834-T-A

158826873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79424601-A-G

158827353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79423984-G-A

158827514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79423835-A-G

158827554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79423795-G-A

158827554-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79423795-G-C

158827704-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79423661-G-C

158827802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79423564-C-T

http://identifiers.org/hco/4/GRCh38#158827899-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79423470-A-C

158827899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79423470-A-G

http://identifiers.org/hco/4/GRCh38#158827904-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79423465-A-C

158828726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79422940-C-T

http://identifiers.org/hco/4/GRCh38#158828869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79422767-C-A

158828874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79422762-C-T

158828928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79422707-T-C

158829038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79422595-T-C

158829140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 79422490-G-A

158829149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 79422481-G-A

158829152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 79422478-G-A

158829158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 79422472-G-A

158829211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 79422422-C-T

http://identifiers.org/hco/4/GRCh38#158829876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79422039-C-A

158829876-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79422039-C-G

158831006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79420984-A-G

158831034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79420960-G-A

158831483-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79420199-T-G

158831498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79420185-T-C

158831732-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79420016-T-A

158831757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79419991-G-T

http://identifiers.org/hco/4/GRCh38#158831768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79419980-C-A

158831768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79419980-C-T

158831789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79419954-T-C

158831829-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79419923-T-A

158832003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79419767-A-G

158832217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79419573-T-C

158832223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79419567-A-G

158832770-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79416388-T-A

158832770-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79416388-T-G

158832850-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79416302-C-G

158832912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79416244-G-A

158833208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79416018-T-C

158833220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79416006-G-A

158833919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79415115-A-G

158833919-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79415115-A-T

http://identifiers.org/hco/4/GRCh38#158834029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79415004-C-A

http://identifiers.org/hco/4/GRCh38#158834031-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79415002-A-C

http://identifiers.org/hco/4/GRCh38#158834036-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79414997-A-C

158834039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79414994-G-A

158834039-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79414994-G-T

http://identifiers.org/hco/4/GRCh38#158834047-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79414986-A-C

http://identifiers.org/hco/4/GRCh38#158834083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79414951-C-A

158834083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79414951-C-T

158834201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79414832-C-T

158834322-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79414689-C-G

http://identifiers.org/hco/4/GRCh38#158834482-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79414452-C-A

158834482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79414452-C-T

158834549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79414388-C-T

158834604-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79414330-T-A

158834779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79414148-G-T

158834818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79414108-A-G

158834914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79414027-G-A

http://identifiers.org/hco/4/GRCh38#158834915-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79414026-A-C

http://identifiers.org/hco/4/GRCh38#158834977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79413971-C-A

158834977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79413971-C-T

158835017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79413931-G-A

http://identifiers.org/hco/4/GRCh38#158835035-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79413913-C-A

158835035-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79413913-C-G

158835146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79413820-G-A

158835146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79413820-G-T

158835209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79413765-A-G

158835209-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79413765-A-T

158835354-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79413632-C-G

http://identifiers.org/hco/4/GRCh38#158835508-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79413485-C-A

158835508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79413485-C-T

158835575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79413427-G-A

158835575-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79413427-G-C

158835575-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79413427-G-T

158835576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79413426-T-C

158835582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79413403-G-A

158835605-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79413376-T-G

158835632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79413349-A-G

158835745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79413243-G-T

http://identifiers.org/hco/4/GRCh38#158835833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79413159-C-A

158835833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79413159-C-T

158836156-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79412871-C-G

158836349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79412668-T-C

158839673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79411693-A-G

http://identifiers.org/hco/4/GRCh38#158839818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79411567-C-A

158839819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79411566-C-T

158839968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79411459-C-T

158840596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79410612-A-G

158840636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79410552-T-C

158840673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79410516-G-A

158840674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79410515-G-A

158840688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79410501-G-A

http://identifiers.org/hco/4/GRCh38#158840819-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79410430-A-C

158840819-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79410430-A-T

158840875-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79410376-T-G

158841015-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79410252-G-C

158841043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79410224-C-T

158842862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79409533-G-A

158851283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79407813-A-G

http://identifiers.org/hco/4/GRCh38#158851347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79407746-C-A

158851347-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 79407746-C-G

158851419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 79407674-A-G

158851494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79407599-G-A

http://identifiers.org/hco/4/GRCh38#158851537-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79407559-C-A

158851537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79407559-C-T

158851540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79407556-T-C

158851578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79407518-A-G

158851621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79407477-A-G

158852067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79406059-T-C

158852292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79405823-C-T

158852509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79405676-G-A

158852625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79405572-C-T

158852668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79405529-C-T

158852785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79404969-G-A

158852797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79404957-G-A

158852842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79404915-A-G

158852891-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79404782-A-T

158853057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79404622-T-C

158855966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: -A-G

158856029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79403765-T-C

158856117-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79403666-G-C

158856565-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79403113-G-C

158856812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79402911-A-G

158857019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79402717-C-T

http://identifiers.org/hco/4/GRCh38#158857071-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79402668-C-A

http://identifiers.org/hco/4/GRCh38#158857091-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79402648-A-C

158857142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79402606-G-A

158857149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79402599-G-A

158857149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79402599-G-T

158857280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79402470-A-G

158857280-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79402470-A-T

158857397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79402262-T-C

158857448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79402213-C-T

158858233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79401903-G-A

158858369-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79401746-G-T

http://identifiers.org/hco/4/GRCh38#158858513-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79401640-A-C

158858840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79401024-T-C

158858952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79400884-T-C

158859193-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, missense_variant, splice_region_variant
orthologous variants: 79400646-T-A

158859193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, missense_variant, splice_region_variant
orthologous variants: 79400646-T-C

158859193-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, missense_variant, splice_region_variant
orthologous variants: 79400646-T-G

158859316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79400476-G-A

158859356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79400441-G-T

158859400-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79400399-T-A

158859400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79400399-T-C

158859400-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79400399-T-G

158859420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79400386-G-A

http://identifiers.org/hco/4/GRCh38#158859463-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79400344-C-A

158859463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79400344-C-T

158859499-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79400308-T-A

158859550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79400251-A-G

158859560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79400243-G-T

158859748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79400055-T-C

http://identifiers.org/hco/4/GRCh38#158859880-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79399747-A-C

158860037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79399578-C-T

http://identifiers.org/hco/4/GRCh38#158860055-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79399558-A-C

158860060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79399553-G-A

158861224-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79396810-T-A

158861224-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79396810-T-G

158861397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: missense variant
orthologous variants: 79396642-A-G

158861516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79396524-A-G

158861532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79396509-C-T

158861534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79396507-A-G

http://identifiers.org/hco/4/GRCh38#158861833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79396204-C-A

158861921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79396124-T-C

158861963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79396086-C-T

158861989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79396060-A-G

http://identifiers.org/hco/4/GRCh38#158862887-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79394550-A-C

158862995-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79394441-C-G

158863063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79394375-T-C

158863140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79394302-G-A

158863524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79393953-A-G

158863600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79393858-C-T

158863624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79393836-T-C

158863655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79393809-T-C

158863675-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79393794-C-G

158863686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79393783-A-G

http://identifiers.org/hco/4/GRCh38#158865967-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79391971-C-A

158865969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79391969-G-A

158866072-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79391867-G-T

158866093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79391858-C-T

158866103-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79391846-T-A

158867698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79389784-A-G

158867979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79389305-A-G

158867980-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79389304-G-T

158868040-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79389244-G-C

158868044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79389240-T-C

158868062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79389223-C-T

http://identifiers.org/hco/4/GRCh38#158868085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79389201-C-A

http://identifiers.org/hco/4/GRCh38#158868107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79389179-C-A

158868107-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: missense variant
orthologous variants: 79389179-C-G

http://identifiers.org/hco/4/GRCh38#158868281-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79389005-A-C

158868281-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: missense variant
orthologous variants: 79389005-A-T

158868296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: missense variant
orthologous variants: 79388990-A-G

158868365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: missense variant
orthologous variants: 79388921-G-A

158868456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: missense variant
orthologous variants: 79388830-G-A

158868456-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: missense variant
orthologous variants: 79388830-G-T

158868498-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: missense variant
orthologous variants: 79388788-G-C

158868606-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: missense variant
orthologous variants: 79388677-C-G

158868606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: missense variant
orthologous variants: 79388677-C-T

158868728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: missense variant
orthologous variants: 79388555-T-C

158868746-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: missense variant
orthologous variants: 79388537-C-G

158868746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: missense variant
orthologous variants: 79388537-C-T

158868836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: missense variant
orthologous variants: 79388447-C-T

158869050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: missense variant
orthologous variants: 79388236-T-C

158869165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: synonymous variant
orthologous variants: 79388123-G-A

158869396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: synonymous variant
orthologous variants: 79387896-A-G

158869434-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79387858-T-A

158869495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79387819-G-A

158869495-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79387819-G-T

158869500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79387814-G-A

158869500-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79387814-G-T

158869797-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79387533-T-G

http://identifiers.org/hco/4/GRCh38#158870173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79387091-C-A

158870173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79387091-C-T

http://identifiers.org/hco/4/GRCh38#158870224-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79387046-C-A

158870224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79387046-C-T

http://identifiers.org/hco/4/GRCh38#158870292-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79386969-A-C

http://identifiers.org/hco/4/GRCh38#158870320-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79386941-A-C

158870398-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 79386863-G-C

158870597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79386689-T-C

158870670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79386632-G-A

158870670-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79386632-G-C

158870862-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79386464-C-G

158871170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79386172-A-G

158871170-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79386172-A-T

158871310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79386030-A-G

158871310-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79386030-A-T

158871466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 79385855-C-T

158871527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79385800-G-A

158871532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79385794-A-G

158871882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79385470-T-C

158872130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79385261-A-G

158872130-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79385261-A-T

158872265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79385124-C-T

158872464-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79384929-T-A

158872673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79384727-A-G

158872833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79384441-G-A

158872840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79384434-C-T

158872976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79384319-T-C

158873847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79383644-C-T

158873892-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79383596-G-T

158875510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79382447-G-T

158876664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79381710-T-C

158877274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79380548-A-G

158877510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79380007-T-C

http://identifiers.org/hco/4/GRCh38#158877519-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79379998-A-C

158877665-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79379886-G-C

158887781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79378757-T-C

158887881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79378654-G-A

158888091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79378472-C-T

158888258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79378317-G-T

158888296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79378288-G-A

158888423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79378168-A-G

158891560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: missense variant
orthologous variants: 79372939-G-A

158891560-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: missense variant
orthologous variants: 79372939-G-C

158891685-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79372813-T-G

158891706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79372790-T-C

158891708-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79372788-T-G

158891929-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79372611-T-A

158891989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79372572-G-A

158892660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79372237-A-G

158892703-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79372197-T-G

158893074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79371866-T-C

158893079-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron variant
orthologous variants: 79371862-T-A

158893411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 79371545-T-C

158893411-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 79371545-T-G

http://identifiers.org/hco/4/GRCh38#158893530-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79371438-C-A

158893530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 79371438-C-T

158893555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79371416-G-T

http://identifiers.org/hco/4/GRCh38#158893666-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79371334-C-A

158893666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79371334-C-T

158893764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79371248-G-A

158893764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79371248-G-T

http://identifiers.org/hco/4/GRCh38#158893800-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79371213-A-C

158893800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79371213-A-G

http://identifiers.org/hco/4/GRCh38#158893806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79371207-C-A

158893806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79371207-C-T

158893848-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79371168-T-A

158893852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79371164-G-A

158894195-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79370911-G-T

158894353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79370852-G-A

158894617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79370794-A-G

158894675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79370738-A-G

158894714-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79370695-T-A

158894763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79370644-T-C

158894833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79370588-G-T

158895032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79370392-G-A

158895049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79370375-G-A

158895090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79370334-A-G

158895124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79370301-A-G

158895185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79370244-A-G

158895414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79370024-A-G

158895424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79370013-T-C

158895527-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79369816-A-T

158895546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79369780-G-A

158895626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79369670-G-A

158895626-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79369670-G-C

158895626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79369670-G-T

158895640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79369656-G-A

158895640-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79369656-G-T

158895727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79369572-T-C

158895731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79369568-A-G

http://identifiers.org/hco/4/GRCh38#158895915-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79369380-C-A

158895915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79369380-C-T

http://identifiers.org/hco/4/GRCh38#158895955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79369331-C-A

158895955-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79369331-C-G

158895955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79369331-C-T

http://identifiers.org/hco/4/GRCh38#158895964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79369320-C-A

158895964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79369320-C-T

http://identifiers.org/hco/4/GRCh38#158896014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79369275-C-A

http://identifiers.org/hco/4/GRCh38#158896585-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79368889-A-C

158896612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79368853-T-C

158903804-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79367777-C-G

158903804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79367777-C-T

158903843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79367740-C-T

http://identifiers.org/hco/4/GRCh38#158904242-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79367403-C-A

158904242-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79367403-C-G

158904376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79367112-G-A

158904376-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79367112-G-C

158904376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79367112-G-T

158904544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79366968-A-G

158904610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79366924-A-G

158904611-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79366923-T-A

158904613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79366921-A-G

http://identifiers.org/hco/4/GRCh38#158904757-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79366784-C-A

http://identifiers.org/hco/4/GRCh38#158904876-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79366676-A-C

158904894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79366657-G-A

158904894-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79366657-G-C

158904894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79366657-G-T

158905008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79366573-C-T

http://identifiers.org/hco/4/GRCh38#158905105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79366481-C-A

158905105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79366481-C-T

158905193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79366392-T-C

158905280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79366332-G-A

158905322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79366299-T-C

158905365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79366260-G-A

158905365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79366260-G-T

158905457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79366167-A-G

158905537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79366102-A-G

158905676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79365962-G-A

http://identifiers.org/hco/4/GRCh38#158905711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79365950-C-A

158905749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79365913-T-C

158905797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79365870-G-A

158905797-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79365870-G-C

158905866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79365810-A-G

http://identifiers.org/hco/4/GRCh38#158905924-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#79365760-A-C

158905966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79365698-T-C

158906014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79365655-T-C

158906096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79365516-G-A

158906096-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79365516-G-T

http://identifiers.org/hco/4/GRCh38#158906186-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79365429-A-C

158906293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79365373-A-G

158906295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79365371-A-G

158906307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79365355-A-G

158906399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79365275-G-T

158906439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79365235-C-T

158906499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79365181-A-G

http://identifiers.org/hco/4/GRCh38#158906596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#79365085-C-A

http://identifiers.org/hco/4/GRCh38#158906796-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79364936-A-C

158906845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79364891-G-A

http://identifiers.org/hco/4/GRCh38#158906921-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79364838-C-A

158907032-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79364732-T-A

158907040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79364724-G-A

158907130-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79364634-T-A

158907550-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79364232-G-T

http://identifiers.org/hco/4/GRCh38#158907851-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79363945-A-C

158907853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79363943-G-A

158907922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29280
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79363863-T-C