http://identifiers.org/hco/16/GRCh38#3027709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23887663-C-A

3027709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23887663-C-T

http://identifiers.org/hco/16/GRCh38#3027766-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23887570-C-A

3027766-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23887570-C-G

3027766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23887570-C-T

http://identifiers.org/hco/16/GRCh38#3027835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23887499-C-A

3027869-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23887440-T-A

3027869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23887440-T-C

3027869-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23887440-T-G

3027921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23887392-T-C

3027922-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23887391-C-G

3027944-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23887371-T-A

3027944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23887371-T-C

3027944-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23887371-T-G

http://identifiers.org/hco/16/GRCh38#3027957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23887358-C-A

3027957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23887358-C-T

3027991-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23887342-G-C

3027991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23887342-G-T

3028022-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23887317-G-T

http://identifiers.org/hco/16/GRCh38#3028034-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23887305-C-A

3028034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23887305-C-T

3028097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23887245-G-A

3028097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23887245-G-T

3028182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 23887160-G-A

3028182-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 23887160-G-T

http://identifiers.org/hco/16/GRCh38#3028183-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23887159-C-A

3028183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 23887159-C-T

3028195-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 23887148-T-A

3028195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 23887148-T-C

3028195-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 23887148-T-G

3028206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 23887142-G-A

3028206-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 23887142-G-C

3028206-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 23887142-G-T

http://identifiers.org/hco/16/GRCh38#3028241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#23887107-C-A

3028241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 23887107-C-T

http://identifiers.org/hco/16/GRCh38#3028322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#23887008-C-A

3028322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23887008-C-T

3028333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23886997-G-A

3028333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23886997-G-T

3028373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 23886956-A-G

3028526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23886801-G-A

3028526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23886801-G-T

http://identifiers.org/hco/16/GRCh38#3028530-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23886797-C-A

3028530-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23886797-C-G

3028530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23886797-C-T

http://identifiers.org/hco/16/GRCh38#3028547-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23886793-C-A

3028547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23886793-C-T

3028555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23886785-A-G

3028604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23886762-G-A

3028612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23886754-G-A

3028612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23886754-G-T

3028632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23886735-G-A

3028632-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23886735-G-C

3028632-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23886735-G-T

http://identifiers.org/hco/16/GRCh38#3028667-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23886681-C-A

3028667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23886681-C-T

http://identifiers.org/hco/16/GRCh38#3028669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23886679-C-A

3028669-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23886679-C-G

3028669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23886679-C-T

http://identifiers.org/hco/16/GRCh38#3028816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23886535-C-A

3028816-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 23886535-C-G

3028823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 23886528-A-G

3028847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23886505-G-A

3028847-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23886505-G-T

http://identifiers.org/hco/16/GRCh38#3028859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23886493-C-A

3028859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23886493-C-T

3028870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23886482-A-G

http://identifiers.org/hco/16/GRCh38#3028941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23886436-C-A

3028941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23886436-C-T

3029245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23886212-G-A

3029245-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23886212-G-T

3029396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 23886065-T-C

http://identifiers.org/hco/16/GRCh38#3029540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#23885923-C-A

3029540-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23885923-C-G

3029609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 23885851-T-C

3029626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 23885834-A-G

http://identifiers.org/hco/16/GRCh38#3029656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23885804-C-A

3029656-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 23885804-C-G

3029656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 23885804-C-T

3029673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 23885787-A-G

3029673-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 23885787-A-T

3029729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 23885731-G-A

3029729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 23885731-G-T

3029848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23885622-G-A

3029848-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23885622-G-T

3029863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23885606-C-T

http://identifiers.org/hco/16/GRCh38#3029928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23885545-C-A

3029928-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23885545-C-G

3029928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23885545-C-T

http://identifiers.org/hco/16/GRCh38#3029995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23885439-C-A

3029995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23885439-C-T

3030054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23885371-A-G

http://identifiers.org/hco/16/GRCh38#3030074-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23885351-A-C

3030074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23885351-A-G

3030074-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23885351-A-T

3030136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23885300-G-A

3030136-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23885300-G-T

3030162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23885273-C-T

3030165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23885270-C-T

http://identifiers.org/hco/16/GRCh38#3030178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23885262-C-A

3030178-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23885262-C-G

3030198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23885253-T-C

3030198-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23885253-T-G

3030208-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23885243-G-T

3030257-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23885199-T-G

http://identifiers.org/hco/16/GRCh38#3030285-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23885171-C-A

3030285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23885171-C-T

3030348-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23885135-C-G

3030450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 23885059-T-C

http://identifiers.org/hco/16/GRCh38#3030608-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23884901-C-A

3030681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23884844-C-T

http://identifiers.org/hco/16/GRCh38#3030720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23884805-C-A

3030720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 23884805-C-T

3030737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 23884788-C-T

http://identifiers.org/hco/16/GRCh38#3030872-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23884636-C-A

http://identifiers.org/hco/16/GRCh38#3030990-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23884520-C-A

3030990-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 23884520-C-G

3030990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 23884520-C-T

3031032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 23884478-T-C

3031206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23884317-G-A

3031206-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23884317-G-T

3031243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23884282-G-A

http://identifiers.org/hco/16/GRCh38#3031283-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23884242-A-C

3031283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23884242-A-G

http://identifiers.org/hco/16/GRCh38#3031337-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23884171-A-C

3031337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23884171-A-G

3031337-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23884171-A-T

3031349-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23884163-A-T

http://identifiers.org/hco/16/GRCh38#3031401-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23884111-A-C

3031401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23884111-A-G

3031418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 23884094-G-A

3031418-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23884094-G-T

3031470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 23884045-T-C

http://identifiers.org/hco/16/GRCh38#3031548-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23883968-C-A

3031548-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23883968-C-G

3031548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23883968-C-T

http://identifiers.org/hco/16/GRCh38#3031666-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#23883823-C-A

3031666-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 23883823-C-G

3031666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 23883823-C-T

http://identifiers.org/hco/16/GRCh38#3031756-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#23883743-C-A

3031756-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 23883743-C-G

3031756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 23883743-C-T

3034051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23882107-G-A

3034051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23882107-G-T

3034058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23882100-G-A

3034192-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23881987-C-G

3034192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23881987-C-T

3034281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23881899-T-C

http://identifiers.org/hco/16/GRCh38#3034525-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23881537-A-C

3034564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23881501-G-A

3034564-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23881501-G-C

3034567-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23881498-C-G

3034567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23881498-C-T

http://identifiers.org/hco/16/GRCh38#3034724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23881337-C-A

3034724-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23881337-C-G

3034724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23881337-C-T

3034832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23881269-G-A

3034832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23881269-G-T

http://identifiers.org/hco/16/GRCh38#3034932-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23881208-C-A

http://identifiers.org/hco/16/GRCh38#3034938-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23881202-C-A

3035020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23881176-A-G

3035020-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23881176-A-T

3035022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23881174-G-A

http://identifiers.org/hco/16/GRCh38#3035043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23881169-C-A

3035049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23881163-G-A

3035049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23881163-G-T

http://identifiers.org/hco/16/GRCh38#3035070-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23881146-A-C

3035070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23881146-A-G

3035070-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23881146-A-T

3035120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23881108-T-C

http://identifiers.org/hco/16/GRCh38#3035180-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23881063-C-A

3035180-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23881063-C-G

3035180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23881063-C-T

3035198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23881046-G-A

3035198-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23881046-G-C

3035198-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23881046-G-T

3035237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23881012-G-A

3035446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 23880803-G-A

3035458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 23880791-C-T

3035621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23880665-G-A

3035621-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23880665-G-C

3035621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23880665-G-T

3035781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23880503-T-C

3035815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23880458-G-A

3035815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23880458-G-T

3035870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23880435-A-G

3035915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23880385-T-C

3035915-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23880385-T-G

3035924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23880376-G-A

3035924-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23880376-G-T

http://identifiers.org/hco/16/GRCh38#3036048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23880245-C-A

3036048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23880245-C-T

http://identifiers.org/hco/16/GRCh38#3036185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23880110-C-A

3036185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23880110-C-T

http://identifiers.org/hco/16/GRCh38#3036287-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23880009-C-A

http://identifiers.org/hco/16/GRCh38#3036414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23879881-C-A

3036789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 23879607-T-C

3036852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33584
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23879565-A-G