http://identifiers.org/hco/3/GRCh38#45755795-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123463277-A-C

45755836-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 123464092-G-T

45755874-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 123464129-T-G

45755964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 123464214-T-C

http://identifiers.org/hco/3/GRCh38#45755999-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123464247-C-A

45755999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 123464247-C-T

45756053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 123464301-G-A

45756053-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 123464301-G-C

45756053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 123464301-G-T

45756164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 123464397-G-A

45756519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 123464670-G-T

45756595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 123464736-A-G

45756697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: -C-T

45757749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123465265-T-C

http://identifiers.org/hco/3/GRCh38#45757775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123465291-C-A

45757775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123465291-C-T

45758370-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 123465475-T-A

45758370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 123465475-T-C

http://identifiers.org/hco/3/GRCh38#45758541-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123465638-A-C

45758541-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123465638-A-T

45758554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123465651-G-A

45758554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123465651-G-T

http://identifiers.org/hco/3/GRCh38#45758756-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123465843-C-A

45758802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123465893-G-A

http://identifiers.org/hco/3/GRCh38#45758891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123465972-C-A

45758891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123465972-C-T

45759032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123466115-C-T

45759043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123466126-G-A

45759043-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 123466126-G-C

http://identifiers.org/hco/3/GRCh38#45759074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123466157-C-A

45759092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123466175-T-C

45759221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123466312-G-A

45759221-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123466312-G-T

45759226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123466317-G-A

45759235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123466325-T-C

45759751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123466742-A-G

45759751-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123466742-A-T

http://identifiers.org/hco/3/GRCh38#45759756-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123466747-C-A

45759756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123466747-C-T

http://identifiers.org/hco/3/GRCh38#45759757-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123466748-C-A

45759757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123466748-C-T

45759887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123466888-G-A

45759887-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123466888-G-T

45759893-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123466894-C-G

45759893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123466894-C-T

45760043-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123467044-G-C

45760079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123467061-G-A

45760079-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123467061-G-T

45760080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123467062-T-C

45760082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123467064-C-T

45760166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123467142-A-G

45760197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123467173-G-A

45760200-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123467176-G-C

45760200-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123467176-G-T

45760216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123467192-G-A

45760235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123467209-G-A

45760411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123467359-C-T

http://identifiers.org/hco/3/GRCh38#45760412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123467360-C-A

45760462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123467409-T-C

45761239-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 123467989-T-A

45761239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 123467989-T-C

45761239-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 123467989-T-G

45761269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 123468018-C-T

45761338-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123468079-C-G

45761339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 123468080-T-C

45761547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123468262-T-C

45761825-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123468461-G-T

45762016-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123468657-G-C

45762060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123468699-C-T

45762453-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123469003-C-G

45762453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123469003-C-T

45762537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123469285-A-G

45762583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123469332-T-C

45762778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123469520-A-G

45762800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123469539-G-A

45762800-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123469539-G-C

45762800-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123469539-G-T

45762801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123469540-A-G

45762805-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123469544-T-A

45762825-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123469546-T-A

45762842-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123469563-G-T

http://identifiers.org/hco/3/GRCh38#45762848-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123469569-C-A

45762848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123469569-C-T

45762984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123469704-C-T

45763053-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 123469773-G-C

45765302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123470550-G-A

45765302-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123470550-G-T

45765329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123470589-C-T

45765453-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123470693-G-T

45765462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123470702-G-A

45765462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123470702-G-T

http://identifiers.org/hco/3/GRCh38#45765479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123470717-C-A

http://identifiers.org/hco/3/GRCh38#45765485-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123470723-C-A

45765485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123470723-C-T

http://identifiers.org/hco/3/GRCh38#45765490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123470728-C-A

45765490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123470728-C-T

45765500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123470742-C-T

45765501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123470743-T-C

http://identifiers.org/hco/3/GRCh38#45765505-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123470747-C-A

45765505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123470747-C-T

45765509-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123470751-G-C

45765509-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123470751-G-T

45768329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123476976-A-G

45768526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123477154-C-T

45769935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123483813-T-C

45769957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123483835-G-A

45769957-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123483835-G-C

45770009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123483885-G-A

http://identifiers.org/hco/3/GRCh38#45770070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123483947-C-A

http://identifiers.org/hco/3/GRCh38#45770123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123483995-C-A

45770123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123483995-C-T

45770318-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 123484177-G-C

45770319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 123484178-C-T

http://identifiers.org/hco/3/GRCh38#45770447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123484334-C-A

45770482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123484371-T-C

45770493-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123484382-T-A

45770493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123484382-T-C

45770563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123484452-A-G

45770571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123484460-A-G

45770605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123484489-G-A

45770622-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123484506-G-C

45770741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123484734-C-T

45770919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123484937-C-T

45771093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123485103-T-C

http://identifiers.org/hco/3/GRCh38#45771119-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123485146-C-A

45771119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123485146-C-T

45771134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123485165-A-G

45771178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123485229-C-T

45771189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123485258-G-A

45771191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123485260-G-A

45771191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123485260-G-T

45771751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123485763-G-A

45771751-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123485763-G-C

45771751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123485763-G-T

http://identifiers.org/hco/3/GRCh38#45771831-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123485793-A-C

45771831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123485793-A-G

http://identifiers.org/hco/3/GRCh38#45771860-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123485820-A-C

45772031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123485985-G-T

45772042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123485996-A-G

http://identifiers.org/hco/3/GRCh38#45772197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123486154-C-A

45772197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123486154-C-T

45772261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123486237-G-A

45772261-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123486237-G-T

45772262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123486238-A-G

45772296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123486272-A-G

45772296-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123486272-A-T

45772398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123486354-T-C

45772401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123486357-G-A

45772401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123486357-G-T

http://identifiers.org/hco/3/GRCh38#45772457-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123486407-C-A

45772457-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123486407-C-G

45772457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123486407-C-T

45772470-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123486424-G-C

45772470-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123486424-G-T

http://identifiers.org/hco/3/GRCh38#45772680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123486643-C-A

45772746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123486709-T-C

45772757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123486716-G-T

45772870-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123486824-C-G

45772870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123486824-C-T

45772872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123486826-G-A

45772875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123486829-C-T

45772878-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123486832-C-G

45772881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123486835-C-T

45772906-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123486858-C-G

45772906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123486858-C-T

45772914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123486866-G-A

45773511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123487318-C-T

45773920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123487632-T-C

45773938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123487650-A-G

45774156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123487879-T-C

45774576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123488223-A-G

45775026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123488729-G-A

45775109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123488896-G-A

45775327-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123489101-G-C

45775327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123489101-G-T

45775614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123489341-G-A

45775614-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123489341-G-C

45775614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123489341-G-T

45775654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123489375-G-A

45775654-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123489375-G-C

45775654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123489375-G-T

45775709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123489420-T-C

45775716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123489427-T-C

45775717-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123489428-C-G

45775717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123489428-C-T

http://identifiers.org/hco/3/GRCh38#45775718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123489429-C-A

45775737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123489448-G-A

45775737-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123489448-G-T

45775819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 123489518-A-G

45775935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123489634-A-G

45775935-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 123489634-A-T

45775947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 123489646-G-T

45775956-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 123489655-A-T

http://identifiers.org/hco/3/GRCh38#45775998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123489696-C-A

45775998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123489696-C-T

45776073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123489768-G-A

http://identifiers.org/hco/3/GRCh38#45777749-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123490219-A-C

45777940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123490354-G-A

45778023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123490391-C-T

45778190-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123490554-T-A

45778190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123490554-T-C

45778190-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123490554-T-G

45779676-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123491765-C-G

45779677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123491766-T-C

45779753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123491834-G-A

http://identifiers.org/hco/3/GRCh38#45779930-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123491955-C-A

45779930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123491955-C-T

45779952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123491972-G-A

45779952-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123491972-G-T

45779983-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123491996-G-C

http://identifiers.org/hco/3/GRCh38#45780006-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123492011-C-A

45780182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123492175-C-T

45780204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123492197-G-A

45780204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123492197-G-T

45780364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123492344-C-T

45780632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123492559-G-A

45780632-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123492559-G-T

45780677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123492604-C-T

45780790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123492709-G-A

45781328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123492976-C-T

45781510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123493121-G-T

45781560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123493157-A-G

45781772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123493330-G-A

45781916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123493466-C-T

45781940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123493491-G-A

45781940-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123493491-G-C

45781940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123493491-G-T

http://identifiers.org/hco/3/GRCh38#45781941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123493492-C-A

45781941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123493492-C-T

45781947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123493498-G-A

45781947-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123493498-G-C

45781947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123493498-G-T

45781951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123493501-A-G

45781956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123493506-A-G

45781960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123493510-A-G

http://identifiers.org/hco/3/GRCh38#45781965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123493513-C-A

http://identifiers.org/hco/3/GRCh38#45781977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123493525-C-A

45781977-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123493525-C-G

http://identifiers.org/hco/3/GRCh38#45782019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123493551-C-A

45782019-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123493551-C-G

45782019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123493551-C-T

http://identifiers.org/hco/3/GRCh38#45782027-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123493559-C-A

45782027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123493559-C-T

http://identifiers.org/hco/3/GRCh38#45782042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123493574-C-A

45782042-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123493574-C-G

45782042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123493574-C-T

45782062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123493594-G-A

45782062-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123493594-G-C

45782062-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123493594-G-T

45782073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123493608-C-T

45782267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123493799-T-C

45782280-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123493806-C-G

45782280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123493806-C-T

45782301-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123493827-T-A

45782301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123493827-T-C

45782328-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123493847-G-C

45782328-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123493847-G-T

45782334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123493853-G-A

45782334-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123493853-G-T

45782346-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123493863-C-G

45782483-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123494012-T-A

http://identifiers.org/hco/3/GRCh38#45782590-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123494106-A-C

45782590-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123494106-A-T

45784360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123494479-G-A

45784360-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123494479-G-T

http://identifiers.org/hco/3/GRCh38#45785973-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123495615-C-A

45786205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123495813-T-C

45786318-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123495866-C-G

45786493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123496030-G-A

45786784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123496421-T-C

45786916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123496552-T-C

http://identifiers.org/hco/3/GRCh38#45790195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123502211-C-A

45790195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123502211-C-T

45790230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123502240-A-G

45790238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123502247-A-G

45790379-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123502322-G-C

45791501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123503354-G-T

45791502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123503355-G-T

45791940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123503395-C-T

45791974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123503422-C-T

45792014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123503473-G-A

45792147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123503620-A-G

45792234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123503675-G-A

45792368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123503760-T-C

45792533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123503918-G-A

45792663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123504166-G-A

45792794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123504317-C-T

45793030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123504499-C-T

45793287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123504730-G-A

45793582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123505056-C-T

45794073-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123505726-T-G

45794109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123505759-A-G

45794636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123506163-A-G

http://identifiers.org/hco/3/GRCh38#45794795-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123506322-A-C

45794864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123506365-C-T

45795115-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123506591-C-G

45795115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123506591-C-T

http://identifiers.org/hco/3/GRCh38#45795126-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123506602-A-C

http://identifiers.org/hco/3/GRCh38#45795512-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123506986-A-C

45795640-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 123507100-T-A

45795893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123507402-T-C

http://identifiers.org/hco/3/GRCh38#45795910-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123507419-A-C

http://identifiers.org/hco/3/GRCh38#45795972-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123507458-A-C

http://identifiers.org/hco/3/GRCh38#45796002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123507493-C-A

45796023-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123507516-G-C

45796038-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123507532-A-T

45796054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123507548-G-A

45796111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123507622-T-C

http://identifiers.org/hco/3/GRCh38#45796145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123507655-C-A

45796146-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123507656-T-G

45796151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123507661-A-G

http://identifiers.org/hco/3/GRCh38#45796198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123507691-C-A

45796216-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123507713-T-A

45796216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123507713-T-C

45796221-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123507718-T-G

45796248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123507727-G-A

45796248-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123507727-G-T

45796285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123507737-C-T

45796291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 123507743-G-A

45796308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123507760-A-G

45796348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 123507800-G-A

45796348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 123507800-G-T

45796390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 123507842-G-A

45796399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 123507851-C-T

45796400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123507852-A-G

http://identifiers.org/hco/3/GRCh38#45796402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#123507854-C-A

45796402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 123507854-C-T

45796427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123507878-G-A

45796427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123507878-G-T

45796430-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123507881-T-A

45796430-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123507881-T-G

45796440-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123507891-C-G

45796440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123507891-C-T

45796472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123507894-T-C

45796482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123507904-G-T

45796485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123507907-G-A

45796485-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123507907-G-C

45796485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30927
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123507907-G-T