28396059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78365953-G-A

28396110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78365902-C-T

28396226-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 78365787-G-C

28396305-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78365708-G-C

http://identifiers.org/hco/17/GRCh38#28396426-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#78365595-A-C

28396426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78365595-A-G

28396426-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78365595-A-T

http://identifiers.org/hco/17/GRCh38#28396438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#78365584-C-A

28396599-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78365448-T-A

28396599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78365448-T-C

28396599-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78365448-T-G

28396612-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78365441-T-A

28396612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78365441-T-C

28396612-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78365441-T-G

http://identifiers.org/hco/17/GRCh38#28396665-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#78365387-A-C

28396665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78365387-A-G

28396665-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78365387-A-T

http://identifiers.org/hco/17/GRCh38#28396677-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#78365375-A-C

28396765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78365308-T-C

28396789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78365285-T-C

28396789-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78365285-T-G

28396990-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78365129-G-T

http://identifiers.org/hco/17/GRCh38#28397078-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#78365060-C-A

28397078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78365060-C-T

28397125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78365013-G-A

28397125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78365013-G-T

28397128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78365010-T-C

http://identifiers.org/hco/17/GRCh38#28397166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#78364980-C-A

28397166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78364980-C-T

http://identifiers.org/hco/17/GRCh38#28397178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#78364968-C-A

28397178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78364968-C-T

28397254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78364896-T-C

http://identifiers.org/hco/17/GRCh38#28397445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#78364738-C-A

28397540-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78364662-G-C

28397540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78364662-G-T

28397544-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78364658-T-A

28397651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78364554-G-A

28397651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78364554-G-T

28397827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78364404-A-G

http://identifiers.org/hco/17/GRCh38#28397864-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#78364369-C-A

28397864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78364369-C-T

28397937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78364302-T-C

28398254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3 prime UTR variant
orthologous variants: 78364045-A-G

http://identifiers.org/hco/17/GRCh38#28398290-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#78364012-C-A

28398290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3 prime UTR variant
orthologous variants: 78364012-C-T

28398317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 78363986-G-A

28398317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 78363986-G-T

28398408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3 prime UTR variant
orthologous variants: 78363896-C-T

http://identifiers.org/hco/17/GRCh38#28398564-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#78363775-C-A

28398588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3 prime UTR variant
orthologous variants: 78363751-A-G

28398595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3 prime UTR variant
orthologous variants: 78363744-G-A

28398595-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3 prime UTR variant
orthologous variants: 78363744-G-C

28398602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3 prime UTR variant
orthologous variants: 78363737-G-A

http://identifiers.org/hco/17/GRCh38#28398613-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#78363726-C-A

28398634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3 prime UTR variant
orthologous variants: 78363696-C-T

28398656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 78363674-G-A

28398656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 78363674-G-T

28398739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 78363606-A-G

28398788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3 prime UTR variant
orthologous variants: 78363556-T-C

http://identifiers.org/hco/17/GRCh38#28398790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#78363554-C-A

28398790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3 prime UTR variant
orthologous variants: 78363554-C-T

http://identifiers.org/hco/17/GRCh38#28398817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#78363535-C-A

http://identifiers.org/hco/17/GRCh38#28398916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#78362855-C-A

http://identifiers.org/hco/17/GRCh38#28398953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#78362822-C-A

28399109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3 prime UTR variant
orthologous variants: 78362686-G-A

28399109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3 prime UTR variant
orthologous variants: 78362686-G-T

http://identifiers.org/hco/17/GRCh38#28399136-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#78362663-C-A

28399136-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3 prime UTR variant
orthologous variants: 78362663-C-G

http://identifiers.org/hco/17/GRCh38#28399138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#78362661-C-A

28399138-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3 prime UTR variant
orthologous variants: 78362661-C-G

28399139-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3 prime UTR variant
orthologous variants: 78362660-T-A

28399139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3 prime UTR variant
orthologous variants: 78362660-T-C

http://identifiers.org/hco/17/GRCh38#28399159-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#78362640-C-A

28399159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3 prime UTR variant
orthologous variants: 78362640-C-T

28399195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3 prime UTR variant
orthologous variants: 78362634-A-G

28399291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3 prime UTR variant
orthologous variants: 78362605-A-G

28399327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3 prime UTR variant
orthologous variants: 78362577-T-C

28399327-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3 prime UTR variant
orthologous variants: 78362577-T-G

http://identifiers.org/hco/17/GRCh38#28399333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#78362571-C-A

28399365-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3 prime UTR variant
orthologous variants: 78362553-T-G

http://identifiers.org/hco/17/GRCh38#28399417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#78362497-C-A

http://identifiers.org/hco/17/GRCh38#28399484-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#78362434-C-A

28399484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3 prime UTR variant
orthologous variants: 78362434-C-T

http://identifiers.org/hco/17/GRCh38#28399552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#78362361-C-A

28399552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 78362361-C-T

28399573-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 78362322-T-G

28399595-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 78362294-A-T

28399633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 78362262-C-T

28399698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, missense_variant, synonymous_variant
orthologous variants: 78362210-A-G

28399782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 78362127-C-T

28399797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 78362115-G-A

28399797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 78362115-G-T

28399800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 78362112-G-A

28400263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 78362021-A-G

28400342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 78361950-G-A

28400342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 78361950-G-T

http://identifiers.org/hco/17/GRCh38#28400416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#78361862-C-A

28400416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 78361862-C-T

http://identifiers.org/hco/17/GRCh38#28400428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#78361850-C-A

http://identifiers.org/hco/17/GRCh38#28400430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#78361848-C-A

28400430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 78361848-C-T

28400467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 78361813-G-A

28400467-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 78361813-G-T

28400625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 78361660-G-A

28400625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 78361660-G-T

28400852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 78361436-G-A

28400852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 78361436-G-T

28400858-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 78361430-T-A

28400858-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 78361430-T-G

http://identifiers.org/hco/17/GRCh38#28400875-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#78361418-C-A

28400875-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 78361418-C-G

28400900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 78361396-T-C

28401093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 78360787-C-T

28401106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 78360774-T-C

28401113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 78360767-T-C

28401712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 78360208-G-A

28401712-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 78360208-G-T

28401751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 78360054-C-T

28401819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 78359867-G-T

28401859-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 78359827-C-G

28401896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 78359789-C-T

http://identifiers.org/hco/17/GRCh38#28401931-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#78359750-C-A

http://identifiers.org/hco/17/GRCh38#28401932-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#78359749-C-A

28402138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 78359629-G-A

28402138-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 78359629-G-C

28402138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 78359629-G-T

28402243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 78359527-T-C

28402403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 78359379-T-C

28402403-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 78359379-T-G

28402404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 78359378-A-G

28402404-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 78359378-A-T

28402433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 78359349-G-A

28402435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 78359347-A-G

28402435-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 78359347-A-T

28402544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 78359297-A-G

28402613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 78359234-G-T

28402628-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 78359219-A-T

http://identifiers.org/hco/17/GRCh38#28402637-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#78359210-A-C

28402637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 78359210-A-G

28402638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 78359209-A-G

28402642-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 78359205-T-A

http://identifiers.org/hco/17/GRCh38#28402715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#78359143-C-A

28402724-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 78359137-T-A

28402724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 78359137-T-C

28402945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 78358973-T-C

28403157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 78358859-G-A

28403157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 78358859-G-T

28403167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 78358847-A-G

28403183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 78358839-T-C

28403240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 78358787-G-A

28403240-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 78358787-G-T

28403269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 78358758-A-G

28403327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 78358716-G-T

28403346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 78358698-G-A

28403346-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 78358698-G-T

28404065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: intron variant
orthologous variants: 78358448-G-A

28404065-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: intron variant
orthologous variants: 78358448-G-T

28404095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: intron variant
orthologous variants: 78358417-A-G

http://identifiers.org/hco/17/GRCh38#28404104-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#78358409-A-C

28404104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: intron variant
orthologous variants: 78358409-A-G

28404131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: intron variant
orthologous variants: 78358382-G-T

28404147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: intron variant
orthologous variants: 78358366-G-A

28404147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: intron variant
orthologous variants: 78358366-G-T

28404214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: intron_variant, undefined
orthologous variants: 78358320-G-A

28404214-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: intron_variant, undefined
orthologous variants: 78358320-G-C

28404214-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: intron_variant, undefined
orthologous variants: 78358320-G-T

28404229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: intron variant
orthologous variants: 78358305-G-A

28404229-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: intron variant
orthologous variants: 78358305-G-T

28404321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 78358239-G-A

28404321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 78358239-G-T

28404395-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 78358211-G-C

28404475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 78358131-C-T

28404629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 78358014-A-G

28404861-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78357782-G-T

28404933-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78357710-T-A

28404933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78357710-T-C

28405035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78357608-G-A

28405035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78357608-G-T

28405380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78357263-G-A

28405380-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78357263-G-T

28405485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78357158-A-G

28405498-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78357145-T-A

http://identifiers.org/hco/17/GRCh38#28405716-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#78356980-C-A

28405716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78356980-C-T

28405781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78356906-T-C

http://identifiers.org/hco/17/GRCh38#28405902-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#78356814-C-A

28405902-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 78356814-C-G

28405902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 78356814-C-T

http://identifiers.org/hco/17/GRCh38#28406007-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#78356709-C-A

28406041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78356675-A-G

http://identifiers.org/hco/17/GRCh38#28406053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#78356663-C-A

28406053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78356663-C-T

28406087-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78356629-T-G

28406117-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78356599-G-T

28406123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78356593-G-A

28406123-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78356593-G-T

http://identifiers.org/hco/17/GRCh38#28406132-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#78356584-C-A

28406132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78356584-C-T

http://identifiers.org/hco/17/GRCh38#28406194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#78356556-C-A

28406194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78356556-C-T

http://identifiers.org/hco/17/GRCh38#28406276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#78356454-C-A

28406276-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78356454-C-G

28406276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78356454-C-T

28406300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78356445-G-A

28406300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78356445-G-T

http://identifiers.org/hco/17/GRCh38#28406313-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#78356432-C-A

28406313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78356432-C-T

28406314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78356431-C-T

28406367-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78356394-G-T

28406442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78356312-G-A

28406442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78356312-G-T

28406534-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 78356228-T-G

28406563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 78356199-A-G

28406612-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 78356158-T-A

28406612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 78356158-T-C

28406664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 78356107-A-G

http://identifiers.org/hco/17/GRCh38#28406687-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#78356084-A-C

28406687-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 78356084-A-T

28406864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 5 prime UTR variant
orthologous variants: 78355869-T-C

http://identifiers.org/hco/17/GRCh38#28406911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#78355818-C-A

28406913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 5 prime UTR variant
orthologous variants: 78355816-T-C

28406938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 5 prime UTR variant
orthologous variants: 78355776-T-C

28406940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30521
most severe consequence: 5 prime UTR variant
orthologous variants: 78355774-G-T