45954470-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75584550-G-C

45954648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75584255-G-A

45954674-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75584228-G-T

45954722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75584180-A-G

45954793-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75584117-G-T

45954794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75584116-C-T

45954980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75583960-T-C

45955132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75583845-T-C

45955382-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75583664-A-T

45955385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75583660-T-C

45955690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75583220-C-T

http://identifiers.org/hco/13/GRCh38#45955747-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75583163-C-A

45955747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75583163-C-T

45955938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75582288-T-C

http://identifiers.org/hco/13/GRCh38#45956388-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75581925-A-C

45956406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75581907-C-T

45956459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75581854-T-C

45956543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75581764-A-G

45956650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75581656-A-G

http://identifiers.org/hco/13/GRCh38#45956651-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75581655-C-A

45956729-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75581591-T-A

45956729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75581591-T-C

45956782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75581541-A-G

http://identifiers.org/hco/13/GRCh38#45956822-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75581500-C-A

45956822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75581500-C-T

http://identifiers.org/hco/13/GRCh38#45956873-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75581448-C-A

45956873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75581448-C-T

http://identifiers.org/hco/13/GRCh38#45956958-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75581364-A-C

45956971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75581351-T-C

45957060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75581265-A-G

http://identifiers.org/hco/13/GRCh38#45957109-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75581219-C-A

45957109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75581219-C-T

45957162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 75581167-G-A

45957363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75580967-G-A

45957363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75580967-G-T

45957370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75580961-T-C

45957370-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75580961-T-G

http://identifiers.org/hco/13/GRCh38#45957371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75580960-C-A

http://identifiers.org/hco/13/GRCh38#45957396-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75580937-A-C

45957396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75580937-A-G

45957678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75580683-A-G

45958141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75577473-C-T

45959455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75576918-T-C

45959455-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75576918-T-G

45962535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75576050-C-T

45962652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75575966-C-T

http://identifiers.org/hco/13/GRCh38#45962698-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75575924-C-A

http://identifiers.org/hco/13/GRCh38#45962952-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75575754-C-A

45963031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75575694-G-A

45963031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75575694-G-T

45963048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75575674-G-A

45963048-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75575674-G-T

http://identifiers.org/hco/13/GRCh38#45963074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75575648-C-A

45963115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75575607-C-T

45963182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75575540-T-C

http://identifiers.org/hco/13/GRCh38#45963233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75575502-C-A

45963244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75575493-A-G

45963276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75575462-G-T

http://identifiers.org/hco/13/GRCh38#45963305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75575423-C-A

45963305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75575423-C-T

http://identifiers.org/hco/13/GRCh38#45963361-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75575360-C-A

45963392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75575331-G-A

45963420-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75575303-T-G

45963486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75575270-A-G

45963487-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75575269-T-A

45963671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75575152-A-G

45963671-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75575152-A-T

45963734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75575108-T-C

45963770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75575076-G-A

45963770-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75575076-G-C

45963770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75575076-G-T

45963803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75575046-G-A

http://identifiers.org/hco/13/GRCh38#45964426-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75574340-C-A

45964426-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75574340-C-G

45964426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75574340-C-T

45965083-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75573677-T-G

http://identifiers.org/hco/13/GRCh38#45965312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75573480-C-A

45965312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75573480-C-T

http://identifiers.org/hco/13/GRCh38#45965494-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75573289-A-C

45965494-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75573289-A-T

45965785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75572913-T-C

45966086-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75572637-T-A

45966156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75572564-T-C

45966161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75572559-C-T

45966321-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75572413-T-C

45966474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75571626-C-T

45966603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75571495-T-C

45966937-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75570345-A-T

45966968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75570314-T-C

45966968-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75570314-T-G

45967398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75569743-A-G

45967421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75569716-G-A

45967421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75569716-G-T

45967657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75569503-A-G

http://identifiers.org/hco/13/GRCh38#45967707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75569453-C-A

45967842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75569330-T-C

45968157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75569049-T-C

http://identifiers.org/hco/13/GRCh38#45968163-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75569043-C-A

45968163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75569043-C-T

45968217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75569002-A-G

45968395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75568836-T-C

45969034-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75568411-C-G

45969034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75568411-C-T

45969173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75568299-G-A

45969173-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75568299-G-C

45969270-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75568208-T-A

45969270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75568208-T-C

45969270-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75568208-T-G

45969278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75568200-G-A

45969307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75568171-T-C

45969332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75568146-T-C

45969356-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75568122-G-C

45969359-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75568119-G-C

45969359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75568119-G-T

45969366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75568112-C-T

45969383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75568095-T-C

45969388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75568090-A-G

45969407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75568071-C-T

45969414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75568064-C-T

45969485-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75567993-T-G

45969533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75567945-T-C

45969704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75567774-T-C

45969814-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75567664-G-C

45969978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 75567499-A-G

45970004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75567473-C-T

45970120-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75567431-C-G

45970120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75567431-C-T

http://identifiers.org/hco/13/GRCh38#45970226-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75567319-A-C

http://identifiers.org/hco/13/GRCh38#45970277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75567280-C-A

45970307-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75567258-T-G

45970312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75567253-G-T

45970370-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75567207-T-A

45970373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75567204-C-T

http://identifiers.org/hco/13/GRCh38#45970430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75567147-C-A

45970504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75567076-G-T

45970594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75566978-T-C

45971030-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75566607-G-C

45971073-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75566570-G-T

45971164-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75566458-T-A

45971164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75566458-T-C

45971270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75566359-G-A

45975066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75565779-A-G

45975631-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75565183-A-T

http://identifiers.org/hco/13/GRCh38#45975667-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75565147-C-A

45975667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75565147-C-T

http://identifiers.org/hco/13/GRCh38#45975684-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75565136-C-A

45975684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75565136-C-T

45975727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75565093-C-T

45975888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75564933-T-C

http://identifiers.org/hco/13/GRCh38#45975936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75564897-C-A

45975936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75564897-C-T

45975939-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75564894-T-G

http://identifiers.org/hco/13/GRCh38#45975967-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75564864-A-C

45976076-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75564778-C-G

http://identifiers.org/hco/13/GRCh38#45976118-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75564741-A-C

45976118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75564741-A-G

http://identifiers.org/hco/13/GRCh38#45976157-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75564702-A-C

45976288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75564572-C-T

45976343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75564518-T-C

45976392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75564473-G-A

45976392-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75564473-G-T

45976849-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75564164-T-A

45976917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75564112-A-G

45977248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75563780-G-A

45977318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75563716-A-G

45977634-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75563464-A-T

45977754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75563349-G-A

http://identifiers.org/hco/13/GRCh38#45977866-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75563240-C-A

45977866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75563240-C-T

45977976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75563156-T-C

45978016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75563111-A-G

45978079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75563054-T-C

45979585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75562240-A-G

45979719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75562130-T-C

45979776-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75562079-T-A

45979776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75562079-T-C

45979798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75562057-T-C

45979818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75562037-T-C

45979822-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75562033-T-G

45979839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75562016-C-T

45979866-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75561989-G-T

45979872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75561983-C-T

45979874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 75561981-T-C

45979875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75561980-G-A

45979875-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75561980-G-C

45979876-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75561979-C-G

45979876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75561979-C-T

45979929-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75561926-C-G

45979929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75561926-C-T

45980050-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75561806-T-G

http://identifiers.org/hco/13/GRCh38#45980085-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75561773-A-C

45980105-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75561751-T-A

45980143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75561703-T-C

http://identifiers.org/hco/13/GRCh38#45985253-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75561356-C-A

45985253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75561356-C-T

45985810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75560622-A-G

45985833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75560599-T-C

45985837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75560595-G-A

45985871-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75560562-G-C

45985871-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75560562-G-T

45987947-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75560185-T-G

45987994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75560083-G-A

45988259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75559824-T-C

45988331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75559751-C-T

45988383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75559686-G-A

45988387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75559682-A-G

45988641-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75559497-T-A

45988641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75559497-T-C

45988650-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75559488-T-A

45988767-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75559368-A-T

45988933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75559196-G-A

45989083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75559049-G-A

45989083-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75559049-G-T

45989086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75559046-G-A

45991307-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75556807-T-A

45991395-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75556739-G-T

46002636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75553911-G-A

http://identifiers.org/hco/13/GRCh38#46003033-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75553615-A-C

46003262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75553393-A-G

46003262-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75553393-A-T

46003286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75553369-G-A

46003342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 75553313-G-A

46003342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 75553313-G-T

46003356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75553300-A-G

http://identifiers.org/hco/13/GRCh38#46003398-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75553249-C-A

46003398-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75553249-C-G

46003476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75553178-A-G

46003724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75552807-C-T

46003984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75552565-T-C

46004230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75552396-T-C

46006432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75551248-A-G

46006456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75551225-T-C

46006456-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75551225-T-G

46006516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75551166-T-C

46006554-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75551128-G-C

46006666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75551070-C-T

46006706-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75551039-T-A

46006706-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75551039-T-G

46006737-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75551008-T-A

46006737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75551008-T-C

46006737-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75551008-T-G

46006880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75550856-G-A

46006880-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75550856-G-C

46007175-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75550596-T-G

46007595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75549933-G-A

46008505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75548762-T-C

46008731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75548558-G-A

46009390-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75548076-C-G

46009402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75548064-G-A

http://identifiers.org/hco/13/GRCh38#46010003-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75547514-A-C

http://identifiers.org/hco/13/GRCh38#46010067-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75547444-C-A

46010159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75547401-C-T

46010243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75547339-T-C

http://identifiers.org/hco/13/GRCh38#46010389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75547199-C-A

46010429-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75547159-T-A

46010520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75547067-A-G

46010520-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75547067-A-T

46010532-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75547055-C-G

46010755-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75547024-C-G

46010830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75546991-T-C

46011151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75546736-T-C

46011166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75546721-C-T

46011177-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75546712-G-T

46011346-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75546548-G-T

http://identifiers.org/hco/13/GRCh38#46011375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75546519-C-A

46011375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75546519-C-T

46011491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75546410-T-C

46011664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75546250-T-C

46011936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75545951-T-C

46014990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75545493-C-T

46015337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75545218-G-A

46015404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75545153-G-A

http://identifiers.org/hco/13/GRCh38#46019181-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75544176-C-A

46019824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75543820-G-A

46020132-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75543634-C-G

46020656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75543128-T-C

46021000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75542897-T-C

46021398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75542547-T-C

46021838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75542157-C-T

46021934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75542090-G-A

46022735-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75541202-A-T

46022920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75541025-T-C

46023153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75540809-C-T

http://identifiers.org/hco/13/GRCh38#46023262-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75540683-A-C

46035975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75536649-A-G

46036354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75536378-T-C

46036474-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75536261-G-C

46036474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75536261-G-T

46037368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75535825-T-C

46037648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75535552-C-T

46038396-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75534997-C-G

46039313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75534271-C-T

46039435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75534155-T-C

46039464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75534134-C-T

http://identifiers.org/hco/13/GRCh38#46039591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75534011-C-A

46042079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75531530-T-C

46042354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75531281-T-C

http://identifiers.org/hco/13/GRCh38#46044194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75530711-C-A

46044221-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75530684-G-T

46044368-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75530544-C-G

46044847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75529828-T-C

http://identifiers.org/hco/13/GRCh38#46044857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75529818-C-A

46044858-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75529817-T-A

46044858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75529817-T-C

46044859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75529816-G-A

46044859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75529816-G-T

http://identifiers.org/hco/13/GRCh38#46045105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75529586-C-A

46045105-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75529586-C-G

46045105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75529586-C-T

http://identifiers.org/hco/13/GRCh38#46045147-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75529547-C-A

46045147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75529547-C-T

46045175-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75529523-T-A

46045175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75529523-T-C

46045175-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75529523-T-G

46045377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75529146-T-C

46045377-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75529146-T-G

http://identifiers.org/hco/13/GRCh38#46045596-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75528928-A-C

46045735-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75528794-T-A

http://identifiers.org/hco/13/GRCh38#46045917-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75528667-A-C

46046087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75528442-C-T

46046280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75528255-T-C

46047293-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75527374-A-T

46047298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75527369-A-G

46047463-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75527244-C-G

http://identifiers.org/hco/13/GRCh38#46047524-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75527192-C-A

46048005-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75526477-C-G

46048005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75526477-C-T

46048171-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75525798-A-T

46049545-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75524552-T-G

46049799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75524313-T-C

46050516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75523724-A-G

46050518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75523722-G-A

46051168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75523240-A-G

46051184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75523224-G-A

46051222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75523190-A-G

46051349-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75523062-T-A

46051349-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75523062-T-G

46051561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75522879-T-C

46051591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75522849-T-C

46052055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75522409-T-C

46052055-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75522409-T-G

http://identifiers.org/hco/13/GRCh38#46052096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75522366-C-A

46052096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75522366-C-T

46052209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75522296-T-C

46052293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75522214-T-C

46052299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75522208-T-C

46052311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75522195-A-G

46052311-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75522195-A-T

http://identifiers.org/hco/13/GRCh38#46052346-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75522150-A-C

46052346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75522150-A-G

46052383-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75522124-A-T

46052461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75522046-C-T

46052590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75521940-A-G

http://identifiers.org/hco/13/GRCh38#46052710-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#75521825-A-C

46052710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75521825-A-G

46052739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20368
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 75521796-A-G